Page last updated: 2024-11-06

fluorodeoxyglucose f18

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Description

Fluorodeoxyglucose F18 (FDG) is a radioactive glucose analog used in Positron Emission Tomography (PET) scans to visualize glucose metabolism in living tissues. It is synthesized by reacting a fluorine-18 atom with a precursor molecule via nucleophilic substitution. FDG is taken up by cells via the glucose transporter and is then phosphorylated by hexokinase, trapping it within the cell. FDG is not metabolized further, allowing its accumulation in tissues with high glucose uptake. FDG PET imaging is commonly used to diagnose and monitor cancer, heart disease, and neurological disorders. It is an important research tool for studying glucose metabolism and for understanding disease processes at the cellular level.'

Fluorodeoxyglucose F18: The compound is given by intravenous injection to do POSITRON-EMISSION TOMOGRAPHY for the assessment of cerebral and myocardial glucose metabolism in various physiological or pathological states including stroke and myocardial ischemia. It is also employed for the detection of malignant tumors including those of the brain, liver, and thyroid gland. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1162) [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

magnesium tanshinoate B: an acitve compound purified from Danshen [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID68614
CHEMBL ID1808698
CHEBI ID49136
CHEBI ID49134
MeSH IDM0029360
PubMed CID6918234
CHEMBL ID39993
MeSH IDM0029360

Synonyms (64)

Synonym
2-deoxy-2-((18)f)fluoro-aldehydo-d-glucose
CHEBI:49136 ,
fluorodeoxyglucose f18
18f fluorodeoxyglucose
63503-12-8
2-deoxy-2-(18f)fluoro-d-glucose
fdg f-18
fludeoxyglucose, f-18
fdg-pet
18-fdg
18f-fluorodeoxyglucose
(18f)-fluorodeoxyglucose
fluorine (18f) fludeoxyglucose
18-f fdg
s8fdg
fluglucoscan
(18f)fluoro-2-deoxyglucose
(18f)-fdg
2-deoxy-2-fluoro-d-glucose, f-18
CHEMBL1808698
d-glucose, 2-deoxy-2-(fluoro-18f)-
2-deoxy-2(f-18)fluoro-2-d-glucose
unii-0z5b2cjx4d
2-deoxy-2-fluoro-18f-d-glucose
2-(18f)fluoro-2-deoxy-d-glucose
(18f)-2-fluoro-2-deoxy-d-glucose
18f-flurodeoxyglucose
2-deoxy-2-(fluoro-18f)-d-glucose
fluorine-18 fluorodeoxyglucose
fludeoxyglucose f 18 [usan]
2-deoxy-2-(18f)fluoroglucose
0z5b2cjx4d ,
fludeoxyglucose (18f) [who-dd]
fludeoxyglucose f 18 [mi]
fludeoxyglucose f 18 [vandf]
fludeoxyglucose (18f) [jan]
fludeoxyglucose f 18 [usp impurity]
fludeoxyglucose ((1)f) [inn]
fludeoxyglucose f-18 [orange book]
fludeoxyglucose f(sup 18) [mi]
DTXSID40212908
DB09502
(2r,3s,4r,5r)-2-(18f)fluoranyl-3,4,5,6-tetrahydroxyhexanal
fluorine-18 2-fluoro-2-deoxy-d-glucose
chebi:49134
2-f18-fluoro-2-deoxy-d-glucose
dtxcid801324219
fludeoxyglucosef 18
fludeoxyglucose f 18 injection
2-f18-fluoro-2-deoxyglucose
fludeoxyglucose f 18 (usp impurity)
fludeoxyglucosef18
fludeoxyglucose f-18 injection
magnesium tanshinoate b
magnesium salvianolate b
lithospermic acid b magnesium salt
CHEMBL39993
8v4r1e4c5y ,
154334-65-3
magnesium lithospermate b [inci]
magnesium tanshinoate b [who-dd]
magnesium, ((1r)-1-(carboxy-.kappa.o)-2-(3,4-dihydroxyphenyl)ethyl (2s,3s)-4-((1e)-3-((1r)-1-(carboxy-.kappa.o)-2-(3,4-dihydroxyphenyl)ethoxy)-3-(oxo-.kappa.o)-1-propenyl)-2-(3,4-dihydroxyphenyl)-2,3-dihydro-7-hydroxy-3-benzofurancarboxylato(2-)-.kappa.o3
magnesium;(2r)-2-[(e)-3-[(2s,3s)-3-[(1r)-1-carboxylato-2-(3,4-dihydroxyphenyl)ethoxy]carbonyl-2-(3,4-dihydroxyphenyl)-7-hydroxy-2,3-dihydro-1-benzofuran-4-yl]prop-2-enoyl]oxy-3-(3,4-dihydroxyphenyl)propanoate
Q27271065

Research Excerpts

Toxicity

ExcerptReferenceRelevance
" Similarly synthesized nonradioactive FDG and Na 18F were not toxic under comparable experimental conditions."( Transient toxicity of 2-deoxy-2-[18F]fluoro-D-glucose in mammalian cells: concise communication.
Adelstein, SJ; Fowler, JG; Kassis, AI; Shiue, CY; Wolf, AP, 1983
)
0.27
" We did a phase I study to identify the dose-limiting toxic effects of imatinib in patients with advanced soft tissue sarcomas including GISTs."( Safety and efficacy of imatinib (STI571) in metastatic gastrointestinal stromal tumours: a phase I study.
Dimitrijevic, S; Donato di Paola, E; Judson, I; Martens, M; Nielsen, OS; Sciot, R; Silberman, S; Stroobants, S; Van Glabbeke, M; van Oosterom, AT; Verweij, J; Webb, A, 2001
)
0.31
" Toxic effects and haematological, biochemical, and radiological measurements were assessed during 8 weeks of follow-up."( Safety and efficacy of imatinib (STI571) in metastatic gastrointestinal stromal tumours: a phase I study.
Dimitrijevic, S; Donato di Paola, E; Judson, I; Martens, M; Nielsen, OS; Sciot, R; Silberman, S; Stroobants, S; Van Glabbeke, M; van Oosterom, AT; Verweij, J; Webb, A, 2001
)
0.31
"Five patients on 500 mg imatinib twice daily had dose-limiting toxic effects (severe nausea, vomiting, oedema, or rash)."( Safety and efficacy of imatinib (STI571) in metastatic gastrointestinal stromal tumours: a phase I study.
Dimitrijevic, S; Donato di Paola, E; Judson, I; Martens, M; Nielsen, OS; Sciot, R; Silberman, S; Stroobants, S; Van Glabbeke, M; van Oosterom, AT; Verweij, J; Webb, A, 2001
)
0.31
" It is concluded that cardiac FDG imaging during clamping is safe and provides excellent image quality, including in patients with diabetes mellitus."( Feasibility, safety and image quality of cardiac FDG studies during hyperinsulinaemic-euglycaemic clamping.
Bax, JJ; Boersma, E; Elhendy, A; Poldermans, D; van Lingen, A; Visser, CA; Visser, FC, 2002
)
0.31
"Cardiac FDG single photon emission computed tomography after Acipimox is a simple and safe approach that renders comparable image quality to that obtained during hyperinsulinemic euglycemic clamping."( Safety and feasibility of cardiac FDG SPECT following oral administration of Acipimox, a nicotinic acid derivative: Comparison of image quality with hyperinsulinemic euglycemic clamping in nondiabetic patients.
Bax, JJ; Boersma, E; Elhendy, A; Poldermans, D; Sloof, GW; Van Lingen, A; Visser, CA; Visser, FC,
)
0.13
" Maximum toxicities were monitored and classified according to the Common Terminology Criteria for Adverse Events (ver."( Full-dose 90Y ibritumomab tiuxetan therapy is safe in patients with prior myeloablative chemotherapy.
Avril, N; Jacobs, SA; Joyce, J; McCook, B; Torok, F; Vidnovic, N, 2005
)
0.33
"Our experience suggests that 90Y ibritumomab tiuxetan treatment is safe for use in patients with prior myeloablative therapy when the general inclusion criteria are fulfilled."( Full-dose 90Y ibritumomab tiuxetan therapy is safe in patients with prior myeloablative chemotherapy.
Avril, N; Jacobs, SA; Joyce, J; McCook, B; Torok, F; Vidnovic, N, 2005
)
0.33
" Because etoposide-induced pulmonary toxicity is an uncommon but serious adverse event, clinicians must be vigilant about the possibility of it, so that the optimal treatment can start as soon as possible."( PET scintigraphy of etoposide-induced pulmonary toxicity.
Biesma, DH; Grutters, JC; Post, MC; Verzijlbergen, JF, 2007
)
0.34
"3%) experienced a grade 3/grade 4 adverse event judged related to pertuzumab; none exhibited grade 3/grade 4 cardiac toxicity."( Efficacy and safety of single-agent pertuzumab, a human epidermal receptor dimerization inhibitor, in patients with non small cell lung cancer.
Dang, TP; Davies, AM; de Vries, DJ; Eberhard, DA; Garland, LL; Herbst, RS; Johnson, BE; Lutzker, SG; Lyons, B; Melenevsky, Y; Mendelson, D; Miller, VA; Natale, RB; Schiller, JH; Van den Abbeele, AD, 2007
)
0.34
" Therefore, at the current rate of 50-100 simulations annually, the addition of PET studies to SBRT simulations is safe for our staff."( Radiation safety issues with positron-emission/computed tomography simulation for stereotactic body radiation therapy.
Blackstock, AW; Hampton, CJ; Hinson, WH; Kearns, WT; McMullen, KP; Stieber, VW; Urbanic, JJ, 2008
)
0.35
" Many adverse reactions and false positive reactions related to radiopharmaceuticals take place every day in hospitals, but most of them are not reported."( Undesirable events with radiopharmaceuticals.
Santos-Oliveira, R, 2009
)
0.35
" Most adverse effects are due to infusion-related reactions, and severe respiratory complications are rare."( [18F]-fluorodeoxyglucose positron emission tomography combined with computed tomography detection of asymptomatic late pulmonary toxicity in patients with non-Hodgkin lymphoma treated with rituximab-containing chemotherapy.
Escalon, MP; Kalkanis, D; Lossos, IS; Paes, F; Serafini, A; Stefanovic, A, 2009
)
0.35
" The aim of this study was to analyze the acute single toxic effects dose of two nonradiochemical labeled compounds in rats."( Acute toxicity of two Alzheimer's disease radiopharmaceuticals: FDDNP and IMPY.
Chang, KW; Chen, CC; Lee, SY; Wang, HE, 2009
)
0.35
" Grade 3-4 toxic effects included neutropenia (n=7), raised alanine aminotransferase concentrations (n=5), peripheral neuropathy (n=5), and hypertension (n=5)."( Efficacy and safety of gemcitabine, oxaliplatin, and bevacizumab in advanced biliary-tract cancers and correlation of changes in 18-fluorodeoxyglucose PET with clinical outcome: a phase 2 study.
Abrams, TA; Allen, JN; Bhargava, P; Blaszkowsky, LS; Chan, JA; Clark, JW; Enzinger, PC; Fuchs, CS; Horgan, K; Jain, SR; Kambadakone, AR; Kwak, EL; Meyerhardt, JA; Muzikansky, A; Ryan, DP; Sahani, DV; Sheehan, S; Stuart, K; Zheng, H; Zhu, AX, 2010
)
0.36
" Our results suggest that auto-cell transplantation therapy using MSC-derived Schwann cells is safe and effective for accelerating the regeneration of transected axons and for functional recovery of injured nerves."( Long-term observation of auto-cell transplantation in non-human primate reveals safety and efficiency of bone marrow stromal cell-derived Schwann cells in peripheral nerve regeneration.
Dezawa, M; Hayashi, T; Iida, H; Itokazu, Y; Kitada, M; Kohama, M; Koshino, K; Matsue, D; Ose, T; Tabata, Y; Takamoto, T; Teramoto, N; Wakao, S; Watabe, H, 2010
)
0.36
"To determine safe surgical margins for soft tissue sarcoma, it is essential to perform a general evaluation of the extent of tumor, responses to auxiliary therapy, and other factors preoperatively using multiple types of diagnostic imaging."( Clinical implications of determination of safe surgical margins by using a combination of CT and 18FDG-positron emission tomography in soft tissue sarcoma.
Arishima, Y; Komiya, S; Nagano, S; Tanimoto, A; Terahara, M; Yokouchi, M; Yoshioka, T; Zemmyo, M, 2011
)
0.37
"Three patients (125 mg cohort) had dose-limiting toxic effects (grade 3 nausea/vomiting, diarrhea)."( Phase I safety, pharmacokinetic, and pharmacodynamic study of the oral phosphatidylinositol-3-kinase and mTOR inhibitor BGT226 in patients with advanced solid tumors.
Anak, Ö; Baselga, J; Birle, D; Chen, LC; Hackl, W; Krop, I; Markman, B; Melendez Cuero, M; Mita, M; Shapiro, GI; Siu, L; Stutvoet, S; Tabernero, J, 2012
)
0.38
" Hence, the current challenge is to develop a new therapeutic strategy maintaining excellent patient outcome while reducing potentially life-threatening late adverse effects."( Interim FDG-PET in Hodgkin lymphoma: a compass for a safe navigation in clinical trials?
Gallamini, A; Kostakoglu, L, 2012
)
0.38
" It has a favorable toxicity profile but may induce unexpected adverse effects, such as an infiammatory reaction in the bladder."( Gefitinib in non-small cell lung carcinoma: a case report of an unusual side effect and complete response in advanced disease.
Brangi, M; Cartenì, G; Chiurazzi, B; Laterza, MM; Riccardi, F,
)
0.13
"3-40 mg/kg) resulted in no dose-limiting toxicities (DLTs); adverse events (AEs) included fatigue, hypotension, abdominal pain, dyspnea, and nausea."( Safety, pharmacokinetics, and pharmacodynamics of the DR5 antibody LBY135 alone and in combination with capecitabine in patients with advanced solid tumors.
Bilic, S; Burris, HA; de Vries, EG; Gietema, JA; Goldbrunner, M; Infante, JR; Oldenhuis, CN; Parker, K; Scott, JW; Sharma, S; Yang, L, 2014
)
0.4
"Short-course pre-operative administration of cetuximab is safe and shows a high rate of (18)FDG-PET response."( Tumour response and safety of cetuximab in a window pre-operative study in patients with squamous cell carcinoma of the head and neck.
Cappoen, N; Duprez, T; Gillain, A; Hamoir, M; Hanin, FX; Lhommel, R; Lonneux, M; Machiels, JP; Magremanne, M; Michoux, N; Reychler, H; Rommel, D; Schmitz, S; Weynand, B, 2013
)
0.39
"In 37 patients receiving dalantercept, the most common treatment-related adverse events were peripheral edema, fatigue, and anemia."( Safety, pharmacokinetics, pharmacodynamics, and antitumor activity of dalantercept, an activin receptor-like kinase-1 ligand trap, in patients with advanced cancer.
Agarwal, N; Attie, KM; Bendell, JC; Blobe, GC; Condon, CH; Gordon, MS; Hurwitz, HI; Jones, SF; McClure, T; Mendelson, DS; Pearsall, AE; Sharma, S; Sherman, ML; Wilson, D; Yang, Y, 2014
)
0.4
" Most of the patients on erlotinib show cutaneous adverse effects."( Erlotinib-induced cutaneous toxicity: findings on 18F-FDG PET/CT imaging.
Bal, C; Gupta, RK; Kumar, K; Kumar, R; Singh, H, 2015
)
0.42
" There were no incidences of anaphylaxis or Grade 4/5 adverse events."( Neoadjuvant triweekly nanoparticle albumin-bound paclitaxel followed by epirubicin and cyclophosphamide for Stage II/III HER2-negative breast cancer: evaluation of efficacy and safety.
Hasebe, T; Hirokawa, E; Kuji, I; Matsuura, K; Osaki, A; Saeki, T; Shigekawa, T; Shimada, H; Sugitani, I; Sugiyama, M; Takahashi, T; Takeuchi, H; Ueda, S; Yamane, T, 2015
)
0.42
"Ipilimumab is a promising novel immunotherapy agent and is associated with a variety of immune-related adverse events (irAE)."( Radiographic Profiling of Immune-Related Adverse Events in Advanced Melanoma Patients Treated with Ipilimumab.
Bailey, ND; Hodi, FS; Keraliya, A; Nishino, M; Ott, PA; Ramaiya, NH; Tirumani, SH, 2015
)
0.42
" Sequential lobar treatment and absence of prior angiosuppressive therapy were both associated with a lower rate of serious adverse events."( Safety, Efficacy, and Prognostic Factors After Radioembolization of Hepatic Metastases from Breast Cancer: A Large Single-Center Experience in 81 Patients.
Bartenstein, P; Fendler, WP; Haug, AR; Jakobs, TF; Lechner, H; Lehner, S; Michl, M; Paprottka, KJ; Paprottka, PM; Todica, A, 2016
)
0.43
"Radioembolization for breast cancer liver metastases shows encouraging local response rates with low incidence of serious adverse events, especially in those patients with sequential lobar treatment or without prior angiosuppressive therapy."( Safety, Efficacy, and Prognostic Factors After Radioembolization of Hepatic Metastases from Breast Cancer: A Large Single-Center Experience in 81 Patients.
Bartenstein, P; Fendler, WP; Haug, AR; Jakobs, TF; Lechner, H; Lehner, S; Michl, M; Paprottka, KJ; Paprottka, PM; Todica, A, 2016
)
0.43
"Cumulative cardiotoxicity is a well-established adverse effect of Adriamycin therapy."( Substantial Increase in Myocardial FDG Uptake on Interim PET/CT May Be an Early Sign of Adriamycin-Induced Cardiotoxicity.
Gorla, AK; Mittal, BR; Parmar, M; Prakash, G; Sood, A, 2016
)
0.43
" There is an ongoing debate as to whether progressive ataxia reflects a delayed therapeutic failure due to disease progression or an adverse effect related to repeated increases of stimulation intensity."( Progressive gait ataxia following deep brain stimulation for essential tremor: adverse effect or lack of efficacy?
Åström, M; Brumberg, J; Buck, AK; Isaias, IU; Lanotte, M; Lehrke, R; Lopiano, L; Marotta, G; Musacchio, T; Pozzi, NG; Reich, MM; Roothans, J; Volkmann, J, 2016
)
0.43
" Adverse events within 30 days of MWA were considered procedure-related complications."( Safety and efficacy of microwave ablation for medically inoperable colorectal pulmonary metastases: Single-centre experience.
Ferguson, CD; Luis, CR; Steinke, K, 2017
)
0.46
"Microwave ablation is safe and efficacious in the local control of colorectal pulmonary metastases."( Safety and efficacy of microwave ablation for medically inoperable colorectal pulmonary metastases: Single-centre experience.
Ferguson, CD; Luis, CR; Steinke, K, 2017
)
0.46
" We analyzed the adverse events related to NACRT and surgical complications following surgery."( Efficacy and Safety of Neoadjuvant Chemoradiotherapy Following Esophagectomy with Japanese-style Extended 3-Field Lymphadenectomy for Thoracic Esophageal Cancer.
Imai, K; Kawakita, Y; Konno, H; Liu, J; Minamiya, Y; Mizusawa, KT; Motoyama, S; Nagaki, Y; Saito, H; Sasaki, T; Sato, Y; Wakita, A, 2017
)
0.46
"Transthoracic esophagectomy with Japanese-style extended 3-field lymph node dissection after NACRT is a safe and powerful treatment."( Efficacy and Safety of Neoadjuvant Chemoradiotherapy Following Esophagectomy with Japanese-style Extended 3-Field Lymphadenectomy for Thoracic Esophageal Cancer.
Imai, K; Kawakita, Y; Konno, H; Liu, J; Minamiya, Y; Mizusawa, KT; Motoyama, S; Nagaki, Y; Saito, H; Sasaki, T; Sato, Y; Wakita, A, 2017
)
0.46
" These study findings confirm that the novel radiotracer would be safe for use in human PET imaging."( Dosimetry and Toxicity Studies of the Novel Sulfonamide Derivative of Sulforhodamine 101([18F]SRF101) at a Preclinical Level.
Bardiès, M; Engler, H; Kreimerman, I; Mora-Ramirez, E; Reyes, L; Savio, E, 2019
)
0.51
" Further studies are necessary to determine if the F-FDG PET/CT could early predict adverse effects of mTOR inhibitors."( Everolimus-induced pulmonary toxicity: Findings on 18F-FDG PET/CT imaging.
Bruna-Muraille, C; Dejust, S; Eymard, JC; Morland, D; Papathanassiou, D; Savoye, AM; Yazbek, G, 2018
)
0.48
"To investigate whether the evaluation of tumors, lymphoid cell-rich organs, and immune-related adverse events (IRAE) with F-FDG PET/CT can predict the efficacy and outcome of immunotherapy."( Predicting Response to Immunotherapy by Evaluating Tumors, Lymphoid Cell-Rich Organs, and Immune-Related Adverse Events Using FDG-PET/CT.
Baratto, L; Hatami, N; Mittra, E; Nobashi, T; Reddy, SA; Srinivas, S; Toriihara, A; Yohannan, TK, 2019
)
0.51
"CD19-targeting chimeric antigen receptor (CAR)-T cell therapy has shown great efficacy in patients with relapsed/refractory non-Hodgkin lymphoma (NHL) but has been associated with serious adverse effects, such as cytokine release syndrome (CRS)."( Role of Fluorodeoxyglucose Positron Emission Tomography/Computed Tomography in Predicting the Adverse Effects of Chimeric Antigen Receptor T Cell Therapy in Patients with Non-Hodgkin Lymphoma.
Chang, AH; Chen, D; Hu, Y; Huang, H; Wang, J; Wei, G; Wu, W; Wu, Z; Xiao, L; Yang, S; Zhang, Y; Zhao, K; Zhao, X, 2019
)
0.51
"To investigate the frequency and imaging features of radiographically evident abdominal immune-related adverse events (irAEs) in patients with metastatic non-small-cell lung cancer (NSCLC) treated with PD-1 inhibitors."( Frequency and imaging features of abdominal immune-related adverse events in metastatic lung cancer patients treated with PD-1 inhibitor.
Adeni, AE; Alessandrino, F; Awad, MM; Nishino, M; Sahu, S; Shinagare, AB; Tirumani, SH, 2019
)
0.51
"Blocking the PD-1 pathway induces immune-related adverse events (irAEs) which often involve the thyroid gland (thyroid irAEs)."( Incidence, features, and prognosis of immune-related adverse events involving the thyroid gland induced by nivolumab.
Fujii, T; Hishizawa, M; Inagaki, N; Kawaguchi-Sakita, N; Kim, YH; Kitamura, M; Kitawaki, T; Matsumoto, S; Nomura, M; Otsuka, A; Saito, R; Sakamori, Y; Sone, M; Taura, D; Yamasaki, T; Yamauchi, I; Yasoda, A, 2019
)
0.51
" Fat necrosis, an immune-related adverse event, can be FDG-avid and mimic malignancy on PET/CT scan."( Nivolumab-Induced Subcutaneous Fat Necrosis: Another FDG-Avid Immune-Related Adverse Event.
Bhargava, P; Flynt, L; Marcal, L, 2020
)
0.56
"Both doses were safe and tolerated."( Safety and target engagement profile of two oxaloacetate doses in Alzheimer's patients.
Anderson, H; Becker, A; Bothwell, R; Brooks, W; Burns, JM; Choi, IY; Clutton, J; Harris, RA; Lee, P; Mahnken, JD; Mosconi, L; Pleen, J; Reed, G; Sherry, E; Swerdlow, RH; Vidoni, ED; Wilkins, HM; Zhang, N, 2021
)
0.62
"1000 mg OAA, taken twice daily for 1 month, is safe in AD patients and engages brain energy metabolism."( Safety and target engagement profile of two oxaloacetate doses in Alzheimer's patients.
Anderson, H; Becker, A; Bothwell, R; Brooks, W; Burns, JM; Choi, IY; Clutton, J; Harris, RA; Lee, P; Mahnken, JD; Mosconi, L; Pleen, J; Reed, G; Sherry, E; Swerdlow, RH; Vidoni, ED; Wilkins, HM; Zhang, N, 2021
)
0.62
"BIMRT may be a safe and effective treatment for patients with peritoneal metastases, especially for patients who cannot undergo surgery."( Safety and Efficacy of the Metabolic Profiling of the BIMRT Utilizing 18F FDG PET-CT.
Dang, YZ; Huang, SG; Li, J; Wang, GD; Zhang, DX; Zhao, HL,
)
0.13
"Immune checkpoint inhibitor and chimeric antigen receptor T-cell therapies are associated with a unique spectrum of complications termed immune-related adverse events (irAEs)."( Abdominal immune-related adverse events: detection on ultrasonography, CT, MRI and 18F-Fluorodeoxyglucose positron emission tomography.
Anderson, MA; Bradley, W; Kilcoyne, A; Kurra, V; Lee, SI; Mojtahed, A, 2021
)
0.62
"Lung toxicity is a rare but serious side effect of sirolimus, a mammalian target of rapamycin inhibitor used as an immunosuppressive agent in solid-organ transplant recipients."( Role of Fluorodeoxyglucose Positron Emission Tomogram Scan in Sirolimus-Induced Lung Toxicity: A Rare Case Report.
Albaiz, F; Alothman, B; Alrasheedi, S; Saleemi, A; Saleemi, S; Shah, YZ, 2020
)
0.56
"In this pilot study, patients with refractory CS treated with infliximab, on top of standard of care, had a reduction in inflammation on FDG-PET/CT and an improvement in LV function, without serious adverse events."( Effectiveness and safety of infliximab in cardiac Sarcoidosis.
Akdim, F; Azzahhafi, J; Bakker, ALM; Grutters, JC; Keijsers, RGM; Mathijssen, H; Post, MC; Swaans, MJ; Veltkamp, M, 2021
)
0.62
" A variety of adverse effects from chemotherapy, targeted therapy, immunotherapy, and radiation therapy are commonly encountered in oncologic patients."( Side Effects of Oncologic Treatment in the Chest: Manifestations at FDG PET/CT.
Bhalla, S; Felder, GJ; Ganeshan, D; Itani, M; Lang, JA,
)
0.13

Pharmacokinetics

ExcerptReferenceRelevance
" The MRI data were acquired with a turbo fast low-angle shot sequence and analyzed using a pharmacokinetic model."( Comparison of pharmacokinetic MRI and [18F] fluorodeoxyglucose PET in the diagnosis of breast cancer: initial experience.
Brix, G; Doll, J; Haberkorn, U; Hawighorst, H; Henze, M; Junkermann, H; Knopp, MV; Lucht, R, 2001
)
0.31
" The development of a PET proliferation probe would be a useful pharmacodynamic tool."( Measuring tumor pharmacodynamic response using PET proliferation probes: the case for 2-[(11)C]-thymidine.
Harris, A; Jones, T; Price, P; Wells, P; West, C, 2004
)
0.32
"The microBC is a compact automated counter allowing real-time measurement of blood radioactivity for pharmacokinetic studies in animals as small as mice."( A new tool for molecular imaging: the microvolumetric beta blood counter.
Archambault, M; Bentourkia, M; Cadorette, J; Convert, L; Lecomte, R; Morin-Brassard, G, 2007
)
0.34
" Inhibition of glucose metabolism measured by (18)F-FDG PET was postulated to serve as a pharmacodynamic marker in everolimus-treated non-small cell lung cancer (NSCLC) patients."( Downregulation of 18F-FDG uptake in PET as an early pharmacodynamic effect in treatment of non-small cell lung cancer with the mTOR inhibitor everolimus.
Bangard, C; Boellaard, R; Dietlein, M; Dimitrijevic, S; Eschner, W; Giaccone, G; Gross, SH; Hayes, W; Hoekstra, OS; Hoetjes, N; Kobe, C; Lammertsma, AA; Nogová, L; Pellas, T; Schmidt, K; Thomas, RK; Wolf, J; Zander, T, 2009
)
0.35
"To evaluate 2-deoxy-2-[(18)F]fluoro-d-glucose positron emission tomography imaging ((18)FDG-PET) as a predictive, noninvasive, pharmacodynamic (PD) biomarker of response following administration of a small-molecule insulin-like growth factor-1 receptor and insulin receptor (IGF-1R/IR) inhibitor, OSI-906."( 18FDG-PET predicts pharmacodynamic response to OSI-906, a dual IGF-1R/IR inhibitor, in preclinical mouse models of lung cancer.
Bugaj, JE; Gokhale, PC; Guleryuz, S; Manning, HC; Mantis, C; McKinley, ET; Wild, R; Zhao, P, 2011
)
0.37
" PF-03814735 was rapidly absorbed and demonstrated linear pharmacokinetics up to 100mg QD; mean terminal half-life ranged from 14."( Phase I, open-label, multicentre, dose-escalation, pharmacokinetic and pharmacodynamic trial of the oral aurora kinase inhibitor PF-03814735 in advanced solid tumours.
Burris, HA; Dumez, H; English, PA; Fowst, C; Gerletti, P; Infante, JR; Jakubczak, JL; Jones, SF; Pierce, KJ; Schöffski, P; Van Mieghem, E; Xu, H, 2011
)
0.37
" This work aims to evaluate F-fluorodeoxyglucose-positron emission tomography (FDG-PET) as a pharmacodynamic (PD) biomarker for linifanib treatment utilizing the Calu-6 model of human non-small cell lung (NSCLC) cancer in SCID-beige mice."( FDG-PET as a pharmacodynamic biomarker for early assessment of treatment response to linifanib (ABT-869) in a non-small cell lung cancer xenograft model.
Albert, DH; Day, M; Fox, GB; Hickson, JA; Luo, Y; Mudd, SR; Refici-Buhr, M; Reuter, DR; Tapang, P; Voorbach, MJ, 2012
)
0.38
" We describe a chemotherapy-refractory patient whose clinical condition necessitated rapid identification of an effective agent in whom we used (18)F-fluorodeoxyglucose-positron emission tomography (FDG-PET)/computed tomographic scanning 48 hours after an initial dose of panitumumab to document a pharmacodynamic response to the antibody."( Early FDG/PET scanning as a pharmacodynamic marker of anti-EGFR antibody activity in colorectal cancer.
Alesi, E; Krystal, GW; Tatum, JL, 2012
)
0.38
" Pharmacokinetic MRI parameters such as the volume transfer constant (K(trans)), the extravascular-extracellular volume fraction (ν(e)), and the blood volume fraction (ν(p)) calculated with the Gd-DTPA AIF and the Gd-DTPA AIF converted from (18)F-FDG AIF normalized with or without blood sample were not statistically different."( Conversion of arterial input functions for dual pharmacokinetic modeling using Gd-DTPA/MRI and 18F-FDG/PET.
Bentourkia, M; Blanchette, M; Croteau, E; Lebel, R; Lecomte, R; Lepage, M; Poulin, E; Tremblay, L, 2013
)
0.39
" In addition to determining the MTD, we evaluated pharmacokinetics of BIIB021 and pharmacodynamic effects of BIIB021 [Hsp70, HER2 extracellular domain (HER2-ECD)]."( A phase 1, dose-escalation, pharmacokinetic and pharmacodynamic study of BIIB021 administered orally in patients with advanced solid tumors.
Banerji, U; Castro, J; Lamanna, N; Mita, M; O'Brien, S; Saif, MW; Stogard, C; Takimoto, C; Von Hoff, D, 2014
)
0.4
" Cmax occurred at approximately 90 minutes and t1/2 was approximately 1 hour across dosing cohorts of 25 to 800 mg BIIB021 twice weekly."( A phase 1, dose-escalation, pharmacokinetic and pharmacodynamic study of BIIB021 administered orally in patients with advanced solid tumors.
Banerji, U; Castro, J; Lamanna, N; Mita, M; O'Brien, S; Saif, MW; Stogard, C; Takimoto, C; Von Hoff, D, 2014
)
0.4
" [(18)F]Fluorodeoxyglucose positron emission tomography (FDG-PET) was performed as a pharmacodynamic marker of mTOR inhibition, and dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI) was performed as an indicator of tumor perfusion changes, at 3 time points."( Phase 1 and pharmacodynamic trial of everolimus in combination with cetuximab in patients with advanced cancer.
Avadhani, AN; Ciunci, CA; Divgi, CR; Englander, S; Flaherty, KT; Giantonio, BJ; Harlacker, K; Kang, HC; O'Dwyer, PJ; Perini, RF; Redlinger, M; Rosen, MA; Schnall, M; Song, HK; Sun, W; Troxel, A, 2014
)
0.4
" Correlative pharmacodynamic markers included tumor metabolic activity and tumor blood flow, which decreased from baseline in 63% and 82% of evaluable patients, respectively, and telangiectasia in eight patients."( Safety, pharmacokinetics, pharmacodynamics, and antitumor activity of dalantercept, an activin receptor-like kinase-1 ligand trap, in patients with advanced cancer.
Agarwal, N; Attie, KM; Bendell, JC; Blobe, GC; Condon, CH; Gordon, MS; Hurwitz, HI; Jones, SF; McClure, T; Mendelson, DS; Pearsall, AE; Sharma, S; Sherman, ML; Wilson, D; Yang, Y, 2014
)
0.4
" This Perspective discusses the use of (18)F-fluorodeoxyglucose-positron emission tomography (FDG-PET) for pharmacodynamic evaluation in a very early phase of treatment to predict clinical outcomes in patients with advanced non-small-cell lung cancer."( Early pharmacodynamic assessment using ¹⁸F-fluorodeoxyglucose positron-emission tomography on molecular targeted therapy and cytotoxic chemotherapy for clinical outcome prediction.
Ando, M; Asami, K; Atagi, S; Ishii, M; Kanazu, M; Kawaguchi, T; Kubo, A; Kusunoki, Y; Maruyama, K; Matsuda, Y; Minomo, S; Ogawa, Y; Takada, M; Uehira, K, 2014
)
0.4
" In pharmacokinetic image analysis, the blood concentration of the imaging compound as a function of time, [i."( Optimization of the reference region method for dual pharmacokinetic modeling using Gd-DTPA/MRI and (18) F-FDG/PET.
Bentourkia, M; Blanchette, M; Croteau, É; Lebel, R; Lecomte, R; Lepage, M; Poulin, É; Tremblay, L, 2015
)
0.42
"An AIF derived from an RR in MRI can be accurately converted into a (18) F-FDG AIF and used in PET pharmacokinetic modeling."( Optimization of the reference region method for dual pharmacokinetic modeling using Gd-DTPA/MRI and (18) F-FDG/PET.
Bentourkia, M; Blanchette, M; Croteau, É; Lebel, R; Lecomte, R; Lepage, M; Poulin, É; Tremblay, L, 2015
)
0.42
" We studied the pharmacodynamic effects of everolimus in resectable non-small cell lung cancer (NSCLC) to inform further development of these agents in lung cancer."( A Translational, Pharmacodynamic, and Pharmacokinetic Phase IB Clinical Study of Everolimus in Resectable Non-Small Cell Lung Cancer.
Auffermann, WF; Bechara, R; Behera, M; Chen, Z; Deng, X; Force, SD; Fu, H; Fu, RW; Gal, AA; Harvey, RD; Khuri, FR; Kim, S; Mendel, J; Miller, DL; Owonikoko, TK; Pickens, A; Ramalingam, SS; Rogatko, A; Rossi, MR; Saba, NF; Sica, GL; Sun, SY; Tighiouart, M; Torres, WE, 2015
)
0.42
" We modeled the pharmacokinetic parameters regarding the nasal cavity and pharynx using mass balance equations, and evaluated the values that were obtained by fitting concentration-time profiles using WinNonlin® software."( Visualization of drug translocation in the nasal cavity and pharmacokinetic analysis on nasal drug absorption using positron emission tomography in the rat.
Cui, Y; Furubayashi, T; Hayashi, T; Hayashinaka, E; Irie, S; Katayama, Y; Nakaoka, T; Okauchi, T; Onoe, K; Ose, T; Sakane, T; Shingaki, T; Tanki, N; Wada, Y; Watanabe, Y; Yamaguchi, M, 2016
)
0.43
" 18F-Fluoro-deoxy-glucose positron emission tomography (18F-FDG PET) is a non-invasive pharmacodynamic imaging biomarker that has become an integral part of drug development."( The use of 18F-Fluoro-deoxy-glucose positron emission tomography (18F-FDG PET) as a non-invasive pharmacodynamic biomarker to determine the minimally pharmacologically active dose of AZD8835, a novel PI3Kα inhibitor.
Barjat, H; Ble, FX; Emmas, SA; Hancox, U; Hudson, K; Lawrie, E; Maynard, J; Polanska, UM; Pritchard, A, 2017
)
0.46
"Our pre-clinical studies support the use of 18F-FDG PET imaging as a sensitive and non- invasive pharmacodynamic biomarker (understanding the role of PI3K signalling in glucose uptake) for AZD8835 with a decrease in 18F-FDG uptake observed at only two hours post treatment."( The use of 18F-Fluoro-deoxy-glucose positron emission tomography (18F-FDG PET) as a non-invasive pharmacodynamic biomarker to determine the minimally pharmacologically active dose of AZD8835, a novel PI3Kα inhibitor.
Barjat, H; Ble, FX; Emmas, SA; Hancox, U; Hudson, K; Lawrie, E; Maynard, J; Polanska, UM; Pritchard, A, 2017
)
0.46
" Pharmacokinetic analyses were accompanied by pharmacodynamics assessment of E by FDG-PET."( Sorafenib and everolimus in patients with advanced solid tumors and KRAS-mutated NSCLC: A phase I trial with early pharmacodynamic FDG-PET assessment.
Abdulla, DSY; Backes, H; Behringer, D; Buettner, R; Eichstaedt, M; Fischer, RN; Franklin, J; Frechen, S; Fuhr, U; Gardizi, M; Junge, L; Kaminsky, B; Kinzig, M; Kobe, C; Limburg, M; Mattonet, C; Merkelbach-Bruse, S; Michels, S; Nogova, L; Ouyang, D; Persigehl, T; Rokitta, D; Scheffler, M; Schnell, R; Sörgel, F; Sos, ML; Stelzer, C; Suleiman, AA; Taubert, M; Tian, Y; Wolf, J, 2020
)
0.56

Compound-Compound Interactions

ExcerptReferenceRelevance
"[(18)F]FDG-PET was combined with microdialysis."( Human adipose tissue glucose uptake determined using [(18)F]-fluoro-deoxy-glucose ([(18)F]FDG) and PET in combination with microdialysis.
Asola, M; Huupponen, R; Knuuti, J; Lönnroth, P; Marjamäki, P; Nuutila, P; Parkkola, R; Peltoniemi, P; Strindberg, L; Virtanen, KA, 2001
)
0.31
"Positron-emitting glucose analogue FDG, combined with microdialysis and tissue analysis, is a feasible method in studying glucose metabolism at the cellular level in animal studies."( 2-[(18)F]fluoro-2-deoxy-D-glucose combined with microdialysis can be used for the comparison of tissue glucose metabolism in obese and lean rats.
Bergman, J; Grönroos, T; Haaparanta, M; Huupponen, R; Nuutila, P; Rouru, J; Solin, O; Virtanen, KA, 2002
)
0.31
"To determine the additional value of [(18)F]FDG-PET in combination with computed tomography (CT) over CT used alone, for evaluating ovarian cancer patients after primary treatment."( Advanced ovarian carcinoma: usefulness of [(18)F]FDG-PET in combination with CT for lesion detection after primary treatment.
Aletti, G; De Cobelli, F; De Marzi, P; Del Maschio, A; Fazio, F; Ferrari, A; Gianolli, L; Landoni, C; Mangili, G; Messa, C; Picchio, M; Sironi, S; Viganò, R; Zangheri, B, 2003
)
0.32
"PET used in combination with CT allows to accurately assess tumor response."( Advanced ovarian carcinoma: usefulness of [(18)F]FDG-PET in combination with CT for lesion detection after primary treatment.
Aletti, G; De Cobelli, F; De Marzi, P; Del Maschio, A; Fazio, F; Ferrari, A; Gianolli, L; Landoni, C; Mangili, G; Messa, C; Picchio, M; Sironi, S; Viganò, R; Zangheri, B, 2003
)
0.32
"To evaluate the results of surgical treatment of patients with ischemic heart disease in combination with intraoperative intramyocardial introduction of the human gene VEGF165 (angiostimulin)."( [New approaches to the treatment of ischemic heart disease: therapeutic angiogenesis in combination with surgical revascularization of the myocardium].
Aslanidi, IP; Bokeriia, LA; Eremeeva, MV; Golukhova, EZ; Kiselev, SL; Kliueva, AF; Lukashkin, MA; Poliakova, ES; Vakhromeeva, MN, 2004
)
0.32
"The aim of this study was to define the recommended dose of oxaliplatin when combined with infusional 5-fluorouracil (5-FU) and concurrent pelvic radiotherapy."( Oxaliplatin combined with infusional 5-fluorouracil and concomitant radiotherapy in inoperable and metastatic rectal cancer: a phase I trial.
Hicks, RJ; Leong, T; Lim-Joon, D; Loi, S; Mackay, J; Michael, M; Mitchell, P; Mukesh, B; Ngan, SY; Rischin, D; Zalcberg, J, 2005
)
0.33
"This study was sought to compare the sensitivity, specificity and accuracy of (1) dual isotope simultaneous acquisition single-photon emission computed tomography (DISA SPECT) myocardial image with (99m)Tc-sestamibi/(18)F-fluorodeoxyglucose ((99m)Tc-MIBI/(18)FDG); (2) low dose dobutamine alone and combined with Isosorbide Dinitrate (ISDN: Isoket) stress two dimensional echocardiography (2DE) to predict regional movement recovery after revascularization (CRV) in patients with old myocardial infarction (OMI) and severe left ventricular dysfunction."( [Head to head comparison of dobutamine alone and combined with nitrate stress echocardiography and 99mTc-MIBI/18FDG myocardial SPECT image for diagnosis of viable myocardium in patients with severe left ventricular dysfunction].
Chen, JL; Chen, ZJ; Gao, RL; He, ZX; Hu, FH; Shi, RF; Tian, YQ; Wang, YW; Yang, WX; Yang, YJ; Ye, L; You, SJ, 2005
)
0.33
"9%) underwent low dose dobutamine 10 microg x kg(-1) x min(-1) (Dob10 microg) and ISDN (286 +/- 31 microg/min) combined with Dob5 microg (ISDN-Dob 5 microg) 2DE and DISA SPECT within one week."( [Head to head comparison of dobutamine alone and combined with nitrate stress echocardiography and 99mTc-MIBI/18FDG myocardial SPECT image for diagnosis of viable myocardium in patients with severe left ventricular dysfunction].
Chen, JL; Chen, ZJ; Gao, RL; He, ZX; Hu, FH; Shi, RF; Tian, YQ; Wang, YW; Yang, WX; Yang, YJ; Ye, L; You, SJ, 2005
)
0.33
" When ISDN combined with Dob5 microg, the sensitivity (91."( [Head to head comparison of dobutamine alone and combined with nitrate stress echocardiography and 99mTc-MIBI/18FDG myocardial SPECT image for diagnosis of viable myocardium in patients with severe left ventricular dysfunction].
Chen, JL; Chen, ZJ; Gao, RL; He, ZX; Hu, FH; Shi, RF; Tian, YQ; Wang, YW; Yang, WX; Yang, YJ; Ye, L; You, SJ, 2005
)
0.33
"Judging tumor residue of hepatocellular carcinoma (HCC) after treatment of transcatheter arterial chemo-embolization (TACE) combined with radiofrequency ablation (RFA) by computed tomography (CT) scan is difficult; while 18-fluorodeoxyglucose-positron emission tomography/CT ((18)FDG-PET/CT) has some advantages in this aspect."( [Evaluating efficacy of transcatheter arterial chemo-embolization combined with radiofrequency ablation on patients with hepatocellular carcinoma by 18FDG-PET/CT].
Fan, WJ; Gu, YK; Huang, JH; Lin, YE; Tan, ZB; Wu, PH; Zeng, YX; Zhang, FJ; Zhang, L; Zhao, M, 2005
)
0.33
" The results of CT and (18)FDG-PET/CT of the 13 patients 2-3 weeks after treatment of TACE combined with RFA were compared."( [Evaluating efficacy of transcatheter arterial chemo-embolization combined with radiofrequency ablation on patients with hepatocellular carcinoma by 18FDG-PET/CT].
Fan, WJ; Gu, YK; Huang, JH; Lin, YE; Tan, ZB; Wu, PH; Zeng, YX; Zhang, FJ; Zhang, L; Zhao, M, 2005
)
0.33
"Of the 13 HCC patients that received 1 course of TACE combined with RFA, 11 had tumor residues which were conformed by fine needle biopsy and digital substraction angiography (DSA)."( [Evaluating efficacy of transcatheter arterial chemo-embolization combined with radiofrequency ablation on patients with hepatocellular carcinoma by 18FDG-PET/CT].
Fan, WJ; Gu, YK; Huang, JH; Lin, YE; Tan, ZB; Wu, PH; Zeng, YX; Zhang, FJ; Zhang, L; Zhao, M, 2005
)
0.33
"(18)FDG-PET/CT is better than CT in judging tumor residue of HCC after treatment of TACE combined with RFA or surgery, and in guiding further treatment of HCC."( [Evaluating efficacy of transcatheter arterial chemo-embolization combined with radiofrequency ablation on patients with hepatocellular carcinoma by 18FDG-PET/CT].
Fan, WJ; Gu, YK; Huang, JH; Lin, YE; Tan, ZB; Wu, PH; Zeng, YX; Zhang, FJ; Zhang, L; Zhao, M, 2005
)
0.33
"To evaluate the use of positron emission tomography using 18F-fluorodeoxyglucose (FDG-PET) to assess early response to pre-operative chemoradiation therapy in combination with external locoregional hyperthermia in patients with oesophageal cancer by correlating the reduction of metabolic activity with histopathologic response."( Monitoring of response to pre-operative chemoradiation in combination with hyperthermia in oesophageal cancer by FDG-PET.
Boellaard, R; Crezee, H; Hoekstra, OS; Hulshof, MC; Omloo, JM; Sloof, GW; ten Kate, FJ; van Lanschot, JJ; Vervenne, WL; Westerterp, M, 2006
)
0.33
"FDG-PET is a promising tool for early response monitoring in patients undergoing chemoradiation therapy in combination with hyperthermia."( Monitoring of response to pre-operative chemoradiation in combination with hyperthermia in oesophageal cancer by FDG-PET.
Boellaard, R; Crezee, H; Hoekstra, OS; Hulshof, MC; Omloo, JM; Sloof, GW; ten Kate, FJ; van Lanschot, JJ; Vervenne, WL; Westerterp, M, 2006
)
0.33
" Clinical data on patients with recurring lymphoma who were treated with second-line chemotherapy (DHAP-VIM-DHAP) followed by autologous stem cell transplantation (ASCT) were collected and combined with the results of FDG-PET performed before and after 2 cycles of reinduction chemotherapy."( Early FDG-PET assessment in combination with clinical risk scores determines prognosis in recurring lymphoma.
Pruim, J; Schot, BW; Sluiter, WJ; Vaalburg, W; van Imhoff, GW; Vellenga, E; Zijlstra, JM, 2007
)
0.34
"5-25 mg/kg) was administered every 3 days for 3 weeks alone or in combination with a single dose of 10 Gy or fractionated RT (3 x 5 Gy)."( VEGF trap in combination with radiotherapy improves tumor control in u87 glioblastoma.
Burd, R; Cardi, C; Daskalakis, C; Dicker, AP; Holash, J; Thakur, M; Wachsberger, PR; Yancopoulos, GD, 2007
)
0.34
"Improved tumor control was seen when RT (either single dose or fractionated doses) was combined with the lowest dose of VEGF Trap (2."( VEGF trap in combination with radiotherapy improves tumor control in u87 glioblastoma.
Burd, R; Cardi, C; Daskalakis, C; Dicker, AP; Holash, J; Thakur, M; Wachsberger, PR; Yancopoulos, GD, 2007
)
0.34
" PET combined with computed tomography (PET/CT) shows the metabolic activity with precise anatomic localization."( Detection of aortic graft infection by 18-fluorodeoxyglucose positron emission tomography combined with computed tomography.
Björck, M; Savitcheva, I; Sörensen, J; Tegler, G; Wanhainen, A, 2007
)
0.34
" This study was conducted to investigate the usefulness of (18)F-FMT PET in combination with fluorine-18-fluorodeoxyglucose ((18)F-FDG) PET for the diagnosis of sarcoidosis in patients with suspected malignancy."( Diagnostic usefulness of fluorine-18-alpha-methyltyrosine positron emission tomography in combination with 18F-fluorodeoxyglucose in sarcoidosis patients.
Endo, K; Hisada, T; Ishizuka, T; Kaira, K; Mori, M; Oriuchi, N; Otani, Y; Sunaga, N; Yanagitani, N, 2007
)
0.34
" Use of (18)F-FMT PET in combination with (18)F-FDG PET may be the effective method to distinguish sarcoidosis from malignancy."( Diagnostic usefulness of fluorine-18-alpha-methyltyrosine positron emission tomography in combination with 18F-fluorodeoxyglucose in sarcoidosis patients.
Endo, K; Hisada, T; Ishizuka, T; Kaira, K; Mori, M; Oriuchi, N; Otani, Y; Sunaga, N; Yanagitani, N, 2007
)
0.34
"The purpose of this study was to describe our experiences and analyze the benefits of video-assisted thoracoscopic surgery (VATS) combined with positron emitted tomography (PET)-computed tomography (CT) in the diagnosis of patients with early (Stage 1) sarcoidosis."( Experiences and benefits of positron emitted tomography-computed tomography (PET-CT) combined with video-assisted thoracoscopic surgery (VATS) in the diagnosis of Stage 1 sarcoidosis.
Chen, JY; Luh, SP; Tsao, TC; Wang, YT; Wu, TC, 2007
)
0.34
" VATS combined with PET-CT can provide more accurate and earlier diagnosis of patients with unknown intrathoracic lesions, including the sarcoidosis."( Experiences and benefits of positron emitted tomography-computed tomography (PET-CT) combined with video-assisted thoracoscopic surgery (VATS) in the diagnosis of Stage 1 sarcoidosis.
Chen, JY; Luh, SP; Tsao, TC; Wang, YT; Wu, TC, 2007
)
0.34
" The aim of this article is to show the first case of focal CHI diagnosed in Spain using PET-CT imaging combined with genetic analysis."( [18F-fluoro-L-DOPA PET-CT imaging combined with genetic analysis for optimal classification and treatment in a child with severe congenital hyperinsulinism].
Arbizu Lostao, J; Azcona San Julián, C; Carracedo, A; Fernández-Marmiesse, A; Garrastachu Zumarrán, P; Martino Casado, E; Richter Echevarría, JA, 2008
)
0.35
" However, 18F-FDG PET/CT in combination with qualitative STIR MRI analysis had a significantly higher capability to detect nodal involvement on an individual-patient basis (96."( The effectiveness of 18F-FDG PET/CT combined with STIR MRI for diagnosing nodal involvement in the thorax.
Ameshima, S; Demura, Y; Fujibayashi, Y; Ishizaki, T; Kimura, H; Miyamori, I; Morikawa, M; Okazawa, H; Sasaki, M; Tsuchida, T, 2009
)
0.35
" A microautoradiographic study combined with immunohistochemistry revealed heavy accumulation of 18F-FDG in inflammatory cells containing peroxidase on day 1 and in cells forming granulation tissue (alpha-smooth muscle actin-positive myofibroblasts and ED2-positive macrophages) on days 2-4 in and around ulcers."( PET and macro- and microautoradiographic studies combined with immunohistochemistry for monitoring rat intestinal ulceration and healing processes.
Kataoka, Y; Mizuma, H; Wada, Y; Watanabe, Y; Yamato, M, 2009
)
0.35
"To evaluate the clinical usefulness of fluorodeoxyglucose (FDG)-PET maximal SUV in combination with CT features for differentiation of adenocarcinoma with bronchioloalveolar carcinoma (BAC) from other subtypes of non-small cell lung cancer (NSCLC)."( Clinical usefulness of the fluorodeoxyglucose (FDG)-PET maximal standardized uptake value (SUV) in combination with CT features for the differentiation of adenocarcinoma with a bronchioloalveolar carcinoma from other subtypes of non-small cell lung cancer
Hwang, SC; Lee, KB; Park, KJ; Sheen, SS; Sun, JS; Yoon, JK; Yoon, SN, 2009
)
0.35
" A few patients have been reported with semantic dementia (SD) combined with MND."( Semantic dementia combined with motor neuron disease.
Chin, J; Go, SM; Jeong, JH; Kim, SH; Na, DL; Seo, SW; Suh, MK, 2009
)
0.35
"To assess the value of F-18-fluorodeoxyglucose positron emission tomography (FDG-PET) combined with CT in critically ill patients suspected of having an infection."( F-18-fluorodeoxyglucose positron emission tomography combined with CT in critically ill patients with suspected infection.
Bleeker-Rovers, CP; Oyen, WJ; Pickkers, P; Simons, KS; van der Hoeven, JG, 2010
)
0.36
" We aimed to define the maximum tolerated dose, toxicity, activity, and pharmacokinetics of oral panobinostat, a pan-deacetylase inhibitor, alone and in combination with docetaxel for the treatment of castration-resistant prostate cancer (CRPC)."( A phase I study of oral panobinostat alone and in combination with docetaxel in patients with castration-resistant prostate cancer.
Anand, A; Dzik-Jurasz, A; Hu, J; Rathkopf, D; Ross, RW; Scher, HI; Tanaka, E; Wong, BY; Woo, MM; Yang, W, 2010
)
0.36
" In arm II, oral panobinostat (15 mg) was administered on the same schedule in combination with docetaxel 75 mg/m(2) every 21 days."( A phase I study of oral panobinostat alone and in combination with docetaxel in patients with castration-resistant prostate cancer.
Anand, A; Dzik-Jurasz, A; Hu, J; Rathkopf, D; Ross, RW; Scher, HI; Tanaka, E; Wong, BY; Woo, MM; Yang, W, 2010
)
0.36
" In the diagnostic evaluation, positron emission tomography combined with computed tomography (PET-CT) made a significant contribution--beyond that which would have been possible if only conventional imaging modalities such as magnetic resonance imaging (MRI) and transthoracic echocardiography (TTE) were utilized--and played a major role in follow-up."( Positron emission tomography combined with computed tomography as an integral component in evaluation of primary cardiac lymphoma.
Huang, YT; Lee, JC; Platts, DG; Slaughter, RE, 2010
)
0.36
" On the basis of promising preclinical data, the safety and tolerability of therapy with the mTOR inhibitor RAD001 in combination with radiation (RT) and temozolomide (TMZ) was evaluated in this Phase I study."( North Central Cancer Treatment Group Phase I trial N057K of everolimus (RAD001) and temozolomide in combination with radiation therapy in patients with newly diagnosed glioblastoma multiforme.
Brown, PD; Buckner, JC; Galanis, E; Giannini, C; Jaeckle, KA; McGraw, S; Peller, PJ; Sarkaria, JN; Uhm, JH; Wu, W, 2011
)
0.37
"All patients received weekly oral RAD001 in combination with standard chemoradiotherapy, followed by RAD001 in combination with standard adjuvant temozolomide."( North Central Cancer Treatment Group Phase I trial N057K of everolimus (RAD001) and temozolomide in combination with radiation therapy in patients with newly diagnosed glioblastoma multiforme.
Brown, PD; Buckner, JC; Galanis, E; Giannini, C; Jaeckle, KA; McGraw, S; Peller, PJ; Sarkaria, JN; Uhm, JH; Wu, W, 2011
)
0.37
" On the basis of these results, the recommended Phase II dosage currently being tested is RAD001 70 mg/week in combination with standard chemoradiotherapy."( North Central Cancer Treatment Group Phase I trial N057K of everolimus (RAD001) and temozolomide in combination with radiation therapy in patients with newly diagnosed glioblastoma multiforme.
Brown, PD; Buckner, JC; Galanis, E; Giannini, C; Jaeckle, KA; McGraw, S; Peller, PJ; Sarkaria, JN; Uhm, JH; Wu, W, 2011
)
0.37
"RAD001 in combination with RT/TMZ and adjuvant TMZ was reasonably well tolerated."( North Central Cancer Treatment Group Phase I trial N057K of everolimus (RAD001) and temozolomide in combination with radiation therapy in patients with newly diagnosed glioblastoma multiforme.
Brown, PD; Buckner, JC; Galanis, E; Giannini, C; Jaeckle, KA; McGraw, S; Peller, PJ; Sarkaria, JN; Uhm, JH; Wu, W, 2011
)
0.37
"(18)F-fluorodeoxyglucose (FDG) positron emission tomography (PET) combined with computed tomography (CT) is a promising new tool for the identification of infectious foci."( Diagnostic value of positron emission tomography combined with computed tomography for evaluating patients with septic shock of unknown origin.
Braune, S; Derlin, T; Kluge, S; Klutmann, S; Mester, J; Nierhaus, A; Wichmann, D, 2012
)
0.38
" We investigated whether mental imagery training combined with electromyogram-triggered electric stimulation improved motor function of the paretic upper extremity in patients with chronic stroke and induced cortical changes."( Cortical changes after mental imagery training combined with electromyography-triggered electrical stimulation in patients with chronic stroke.
Choi, JB; Hong, IK; Lee, JH, 2012
)
0.38
"Fourteen subjects with chronic stroke (≥12 months) were randomly allocated to receive mental imagery training combined with electromyogram-triggered electric stimulation (n=7) or generalized functional electric stimulation (n=7) on the forearm extensor muscles of the paretic extremity in 2 20-minute daily sessions 5 days a week for 4 weeks."( Cortical changes after mental imagery training combined with electromyography-triggered electrical stimulation in patients with chronic stroke.
Choi, JB; Hong, IK; Lee, JH, 2012
)
0.38
"The group receiving mental imagery training combined with electromyogram-triggered electric stimulation exhibited significant improvements in the upper extremity component of the Fugl-Meyer Motor Assessment after intervention (median, 7; interquartile range, 5-8; P<0."( Cortical changes after mental imagery training combined with electromyography-triggered electrical stimulation in patients with chronic stroke.
Choi, JB; Hong, IK; Lee, JH, 2012
)
0.38
"Mental imagery training combined with electromyogram-triggered electric stimulation improved motor function of the paretic extremity in patients with chronic stroke."( Cortical changes after mental imagery training combined with electromyography-triggered electrical stimulation in patients with chronic stroke.
Choi, JB; Hong, IK; Lee, JH, 2012
)
0.38
"The aim of this study was to assess the diagnostic performance of fluorodeoxyglucose-positron emission tomography/computed tomography (FDG-PET/CT) in combination with ultrasonography-guided fine needle aspiration cytology (US-guided FNAC) for the preoperative diagnosis of axillary lymph node (ALN) metastases in patients with breast cancer."( Diagnostic performance of fluorodeoxyglucose-positron emission tomography/computed tomography combined with ultrasonography-guided fine needle aspiration cytology for identifying axillary lymph node status in patients with breast cancer.
Katayama, T; Kubota, K; Machida, Y; Shibuya, H; Toriihara, A, 2013
)
0.39
"The allogenic UCB therapy combined with rhEPO in the present study was safe and suggested potential therapeutic efficacy for patients with TBI."( Allogenic umbilical cord blood therapy combined with erythropoietin for patients with severe traumatic brain injury: three case reports.
Jang, SJ; Kang, MS; Kim, M; Kim, SH; Lee, JH; Min, K; Song, J, 2013
)
0.39
"The significance of (18)F-2-deoxy-2-fluoro-glucose positron emission tomography combined with computed tomography imaging (FDG-PET/CT) in the diagnosis of gastric cancer remains controversial."( Assessment of (18)F-fluorodeoxyglucose positron emission tomography combined with computed tomography in the preoperative management of patients with gastric cancer.
Hanazaki, K; Kobayashi, M; Namikawa, T; Nogami, M; Ogawa, Y; Okabayshi, T, 2014
)
0.4
" Overall, i-PET was highly and independently predictive of any outcome, and its negative predictive value was improved by combination with IPI."( Quantitative and qualitative analysis of metabolic response at interim positron emission tomography scan combined with International Prognostic Index is highly predictive of outcome in diffuse large B-cell lymphoma.
André, M; Bosly, A; Bouazza, S; Costantini, S; Lhommel, R; Michaux, L; Mounier, N; Nols, N; Sonet, A; Van Den Neste, E; Vander Borght, T; Vekemans, MC, 2014
)
0.4
" The recommended phase 2 dose of oral weekly everolimus is 70 mg in combination with standard cetuximab."( Phase 1 and pharmacodynamic trial of everolimus in combination with cetuximab in patients with advanced cancer.
Avadhani, AN; Ciunci, CA; Divgi, CR; Englander, S; Flaherty, KT; Giantonio, BJ; Harlacker, K; Kang, HC; O'Dwyer, PJ; Perini, RF; Redlinger, M; Rosen, MA; Schnall, M; Song, HK; Sun, W; Troxel, A, 2014
)
0.4
"Complete insulin suppression combined with markedly increased circulating FFAs does not completely suppress physiological myocardial 18F-FDG uptake and thus conveys no extra diagnostic value compared with extended fasting."( Complete somatostatin-induced insulin suppression combined with heparin loading does not significantly suppress myocardial 18F-FDG uptake in patients with suspected cardiac sarcoidosis.
Bendstrup, E; Christensen, NL; Gormsen, LC; Nielsen, SS; Tolbod, LP, 2013
)
0.39
", in a week-on/week-off schedule, combined with FOLFIRI or FOLFOX."( Intermittent dosing of axitinib combined with chemotherapy is supported by (18)FLT-PET in gastrointestinal tumours.
Bendell, JC; Burris, HA; Hoh, CK; Infante, JR; Kim, S; Reid, TR; Rosbrook, B; Tarazi, J, 2014
)
0.4
"Axitinib administered in a week-on/week-off schedule combined with FOLFIRI or FOLFOX is supported by (18)FLT-PET data and was well tolerated in patients with gastrointestinal tumours."( Intermittent dosing of axitinib combined with chemotherapy is supported by (18)FLT-PET in gastrointestinal tumours.
Bendell, JC; Burris, HA; Hoh, CK; Infante, JR; Kim, S; Reid, TR; Rosbrook, B; Tarazi, J, 2014
)
0.4
" We hypothesized that the combination with rationally selected other therapeutic agents may improve response."( Temsirolimus combined with cisplatin or bevacizumab is active in osteosarcoma models.
Boerman, OC; Fleuren, ED; Flucke, UE; Franssen, GM; Houghton, PJ; Oyen, WJ; Roeffen, MH; van der Graaf, WT; Versleijen-Jonkers, YM, 2014
)
0.4
" This prospective pilot study aimed to assess (18)F-fluorodeoxyglucose positron emission tomography (FDG-PET), combined with whole-body computed tomographic angiography (CTA), in patients with suspected severe sepsis and for whom the prior diagnostic workup had been inconclusive."( ¹⁸F-fluorodeoxyglucose positron emission tomography combined with whole-body computed tomographic angiography in critically ill patients with suspected severe sepsis with no definite diagnosis.
Bollaert, PE; Chevalier-Mathias, E; Gibot, S; Lemarié, J; Mandry, D; Marie, PY; Olivier, P; Roch, V; Tatopoulos, A, 2014
)
0.4
" In this study, we investigated the utility of 13N-ammonia and its combination with 18F-FDG in differentiating brain abscess from necrotic high-grade gliomas."( 13N-ammonia combined with 18F-FDG could discriminate between necrotic high-grade gliomas and brain abscess.
Chen, Z; Shi, X; Tang, G; Wang, X; Yi, C; Zhang, B; Zhang, X, 2015
)
0.42
"13N-ammonia is effective in distinguishing brain abscess from necrotic high-grade gliomas, and its combination with 18F-FDG could further elevate the diagnostic accuracy."( 13N-ammonia combined with 18F-FDG could discriminate between necrotic high-grade gliomas and brain abscess.
Chen, Z; Shi, X; Tang, G; Wang, X; Yi, C; Zhang, B; Zhang, X, 2015
)
0.42
"To explore the preoperative diagnostic value of ¹⁸F-fluorodexyglucose positron emission tomography combined with contrast enhanced computed tomography (¹⁸F-FDG PET-ceCT) in patients with colorectal cancer liver metastasis."( [Diagnostic value of ¹⁸F-fluorodexyglucose positron emission tomography combined with contrast enhanced computed tomography in colorectal cancer liver metastasis].
Chen, F; Hu, P; Hu, R; Liao, S; Lyu, Q; Zhang, J; Zhang, Z, 2015
)
0.42
"To estimate the diagnostic accuracy of sentinel node biopsy (SNB) combined with preoperative (18) F-fluorodeoxyglucose positron emission tomography/computed tomography (FDG PET/CT) for inguinal lymph node (LN) evaluation in patients with invasive penile squamous cell carcinoma (PSCC) with no clinical evidence of inguinal metastases (cN0) at two tertiary centres with complete clinical follow-up."( DaPeCa-3: promising results of sentinel node biopsy combined with (18) F-fluorodeoxyglucose positron emission tomography/computed tomography in clinically lymph node-negative patients with penile cancer - a national study from Denmark.
Alslev, L; Bouchelouche, K; Costa, JC; Høyer, S; Ipsen, P; Jakobsen, JK; Jensen, JB; Krarup, KP; Nerstrøm, H; Sommer, P; Toft, BG, 2016
)
0.43
" The primary endpoints were the sensitivity, specificity, and false-negative rate of SNB combined with FDG PET/CT."( DaPeCa-3: promising results of sentinel node biopsy combined with (18) F-fluorodeoxyglucose positron emission tomography/computed tomography in clinically lymph node-negative patients with penile cancer - a national study from Denmark.
Alslev, L; Bouchelouche, K; Costa, JC; Høyer, S; Ipsen, P; Jakobsen, JK; Jensen, JB; Krarup, KP; Nerstrøm, H; Sommer, P; Toft, BG, 2016
)
0.43
"We examined 254 groins in 129 patients by SNB combined with FDG PET/CT."( DaPeCa-3: promising results of sentinel node biopsy combined with (18) F-fluorodeoxyglucose positron emission tomography/computed tomography in clinically lymph node-negative patients with penile cancer - a national study from Denmark.
Alslev, L; Bouchelouche, K; Costa, JC; Høyer, S; Ipsen, P; Jakobsen, JK; Jensen, JB; Krarup, KP; Nerstrøm, H; Sommer, P; Toft, BG, 2016
)
0.43
"We describe 10 cases of diffuse large B-cell lymphoma (DLBCL) confined to the bone marrow (BM), spleen, and liver, as evidenced by the uniformly increased uptake of fluorodeoxyglucose (FDG) on positron emission tomography combined with computed tomography (PET/CT)."( A unique subtype of diffuse large B-cell lymphoma primarily involving the bone marrow, spleen, and liver, defined by fluorodeoxyglucose-positron emission tomography combined with computed tomography.
Akasaka, T; Fukutsuka, K; Honjo, G; Iioka, F; Izumi, K; Kamoda, Y; Kitamura, K; Misaki, T; Nagai, Y; Nakagwa, M; Ohno, H; Okumura, A; Toda, Y, 2016
)
0.43
" We prospectively evaluated the long-term seizure and cognitive outcomes of MHT combined with multiple subpial transection or lesionectomy (MHT + MST/L)."( Long-term outcome and neuroradiologic changes after multiple hippocampal transection combined with multiple subpial transection or lesionectomy for temporal lobe epilepsy.
Aoki, S; Ibayashi, K; Kamada, K; Kawai, K; Kubota, M; Kunii, N; Matsuo, T; Momose, T; Saito, N; Takahashi, M; Usami, K, 2016
)
0.43
" The present case reports an extremely rare case of HLRCC syndrome combined with adrenocortical carcinoma."( Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome Combined With Adrenocortical Carcinoma on 18F-FDG PET/CT.
Chen, H; Fu, H; Guo, X; Wu, H, 2017
)
0.46
" Using patients with pulmonary nodules as a study model, we hypothesized that IMI with a folate receptor targeted near-infrared contrast agent (OTL38) can improve malignant pulmonary nodule identification when combined with PET."( Intraoperative Molecular Imaging Combined With Positron Emission Tomography Improves Surgical Management of Peripheral Malignant Pulmonary Nodules.
Baldassari, MP; Barbosa, EM; Connolly, C; Delikatny, EJ; Deshpande, C; Drebin, J; Dunbar, A; Keating, J; Kucharczuk, JC; Kularatne, SA; Low, P; Mizelle, J; Newton, AD; Okusanya, O; Predina, JD; Singhal, S; Xia, L, 2017
)
0.46
" We examined F-fluoro-deoxy-glucose positron emission tomography combined with computed tomography (FDG-PET/CT)'s value in ruling out cancer or infection in patients with AAV."( 18F-fluoro-deoxy-glucose positron emission tomography combined with computed tomography can reliably rule-out infection and cancer in patients with anti-neutrophil cytoplasmic antibody-associated vasculitis suspected of disease relapse.
Frary, EC; Gerke, O; Hess, S; Laustrup, H, 2017
)
0.46
"The aim of the study was to investigate the value of F-fluorodeoxyglucose positron-emission tomography combined with computed tomography (F-FDG-PET/CT) in diagnosing native valve endocarditis (NVE)."( 18F-fluorodeoxyglucose positron-emission tomography combined with computed tomography as a diagnostic tool in native valve endocarditis.
Aarntzen, EHJG; Berrevoets, MAH; Bleeker-Rovers, CP; de Geus-Oei, LF; de Vries, J; Kouijzer, IJE; Oyen, WJG; van Dijk, APJ, 2018
)
0.48
"To investigate and discuss the clinical value of positron emission tomography-computed tomography (PET-CT) combined with ultrasound in detection of primary tumors in patients with malignant ascites (MA)."( Clinical Value of Positron Emission Tomography-Computed Tomography Combined with Ultrasound in Detection of Primary Tumors in Patients with Malignant Ascites.
Gou, B; Liu, G; Liu, J; Liu, X; Wang, Y; You, L; Zhu, X, 2019
)
0.51
"7%), and PET-CT combined with abdominal B-ultrasound had the highest sensitivity and accuracy in diagnosing the primary foci of MA (98."( Clinical Value of Positron Emission Tomography-Computed Tomography Combined with Ultrasound in Detection of Primary Tumors in Patients with Malignant Ascites.
Gou, B; Liu, G; Liu, J; Liu, X; Wang, Y; You, L; Zhu, X, 2019
)
0.51
"The PET-CT combined with ultrasound is conducive to improving the diagnostic efficiency for primary tumors in patients with MA."( Clinical Value of Positron Emission Tomography-Computed Tomography Combined with Ultrasound in Detection of Primary Tumors in Patients with Malignant Ascites.
Gou, B; Liu, G; Liu, J; Liu, X; Wang, Y; You, L; Zhu, X, 2019
)
0.51
" He received 3 cycles of radiopeptide therapy using [Lu]Lutetium-DOTATATE combined with temozolomide."( Dual Imaging With 68Ga-DOTATOC and 18F-FDG PET for Planning and Follow-up of PRRT in Combination With Temozolomide Treatment in a Patient With a Metastatic Neuroendocrine Tumor.
Ahmadzadehfar, H; Hain, S; Hartmann, L; Hirzebruch, S; Wei, X, 2019
)
0.51
"The study is to evaluate biodistribution, dosimetry, safety, and clinical usefulness of F-AlF-NOTA-octreotide (F-OC) PET/CT in combination with F-FDG PET/CT for detection of neuroendocrine neoplasms (NENs)."( Clinical Application of 18F-AlF-NOTA-Octreotide PET/CT in Combination With 18F-FDG PET/CT for Imaging Neuroendocrine Neoplasms.
Chen, D; Hu, S; Li, J; Li, Y; Li, Z; Liu, Z; Long, T; Tang, Y; Yang, N; Zhou, M, 2019
)
0.51
"We report a case of a patient with chronic inflammatory rheumatism, psoriasis and Hashimoto thyroiditis and subsequent appearance of static and dynamic ataxia and episodic memory deficit who was diagnosed as PLE combined with small cell lung cancer (SCLC)."( The role of 18F-FDG PET/CT in management of paraneoplastic limbic encephalitis combined with small cell lung cancer: A case report.
Capoccetti, F; Castagnoli, H; Fattori, S; Manni, C; Marchesani, F; Rossi, G, 2019
)
0.51
"To investigate the diagnostic value of ultrasound combined with computed tomography (CT) in pancreatic cancer."( Ultrasound combined with computed tomography in pancreatic cancer.
Huang, X; Li, X; Liu, L; Ma, L; Yang, X; Zhao, X,
)
0.13
" A hundred and one patients with ultrasonic diagnosis were enrolled into the ultrasound group, 98 patients with CT diagnosis were enrolled into CT group, and 113 patients undergoing ultrasound combined with CT diagnosis were enrolled into combined group."( Ultrasound combined with computed tomography in pancreatic cancer.
Huang, X; Li, X; Liu, L; Ma, L; Yang, X; Zhao, X,
)
0.13
"Ultrasound combined with CT can make up for the deficiency of each other and effectively improve the predictive value in the diagnosis of pancreatic cancer, which can be used as an effective examination method in the diagnosis of this disease."( Ultrasound combined with computed tomography in pancreatic cancer.
Huang, X; Li, X; Liu, L; Ma, L; Yang, X; Zhao, X,
)
0.13
" Both plasma Aβ42/40 ratio alone or combined with an FDG-PET-based biomarker of neurodegeneration were assessed as potential AD biomarkers."( Plasma Aβ42/40 ratio alone or combined with FDG-PET can accurately predict amyloid-PET positivity: a cross-sectional analysis from the AB255 Study.
Alegret, M; Arbizu, J; Boada, M; Buendía, M; Guillen, F; Hernández, I; Martínez-Lage, P; Monleón, I; Munuera, J; Pérez-Grijalba, V; Pesini, P; Prieto, E; Romero, J; Ruiz, A; San-José, I; Sarasa, L; Sarasa, M; Sotolongo-Grau, O; Tárraga, L, 2019
)
0.51
"This exploratory study suggests that FES-PET heterogeneity may potentially identify the subset of ER positive, metastatic breast cancer patients who benefit from letrozole combined with CDK inhibition."( Molecular imaging to identify patients with metastatic breast cancer who benefit from endocrine treatment combined with cyclin-dependent kinase inhibition.
Boers, J; de Vries, EFJ; Elias, SG; Glaudemans, AWJM; Hospers, GAP; Kwee, TC; Martens, JWM; Schröder, CP; Schuuring, E; Venema, CM, 2020
)
0.56
"To explore the clinical application value of 18F-fluorodeoxyglucose (18F-FDG) PET/CT imaging combined with detection of serum tumor molecular markers (carbohydrate antigen 125 (CA 125) and human epididymis protein 4 (HE4)) in the diagnosis of recurrence and metastasis of ovarian cancer."( The value of 18F-FDG PET/CT imaging combined with detection of CA125 and HE4 in the diagnosis of recurrence and metastasis of ovarian cancer.
Cui, XW; Gu, L; Li, YS; Sun, J; Wang, SY; Wang, XN; Yin, Q, 2020
)
0.56
"Clinical data about 18F-FDG PET/CT imaging and serum CA125 and HE4 of 69 ovarian cancer patients after the first cytoreductive surgery and chemotherapy were retrospectively analyzed, and the clinical application value of 18F-FDG PET/CT imaging combined with detection of CA125 and HE4 in the diagnosis of recurrence and metastasis of ovarian cancer was evaluated."( The value of 18F-FDG PET/CT imaging combined with detection of CA125 and HE4 in the diagnosis of recurrence and metastasis of ovarian cancer.
Cui, XW; Gu, L; Li, YS; Sun, J; Wang, SY; Wang, XN; Yin, Q, 2020
)
0.56
" In addition, the sensitivity and specificity of 18F-FDG PET/CT combined with detection of serum CA125 and HE4 for the diagnosis were 100."( The value of 18F-FDG PET/CT imaging combined with detection of CA125 and HE4 in the diagnosis of recurrence and metastasis of ovarian cancer.
Cui, XW; Gu, L; Li, YS; Sun, J; Wang, SY; Wang, XN; Yin, Q, 2020
)
0.56
"18F-FDG PET/CT imaging combined with detection of serum CA125 and HE4 can significantly improve the diagnostic efficiency to recurrence and metastasis of ovarian cancer and is conducive to the early diagnosis of the recurrence and metastasis, which provides a basis for further clinical intervention."( The value of 18F-FDG PET/CT imaging combined with detection of CA125 and HE4 in the diagnosis of recurrence and metastasis of ovarian cancer.
Cui, XW; Gu, L; Li, YS; Sun, J; Wang, SY; Wang, XN; Yin, Q, 2020
)
0.56
" More and more evidence shows that 11C-2β-carbomethoxy-3β-(4-fluorophenyl) tropane positron emission tomography ( 11C-CFT PET) combined with 18F-fluorodeoxyglucose positron emission tomography (18F-FDG PET) can effectively improve the accuracy of early diagnosis."( Efficacy of 11C-2β-carbomethoxy-3β-(4-fluorophenyl) tropane positron emission tomography combined with 18F-fluorodeoxyglucose positron emission tomography in the diagnosis of early Parkinson disease: A protocol for systematic review and meta analysis.
Feng, Z; Jiang, L; Li, P; Shao, H; Shi, X; Wang, X, 2020
)
0.56
"We will integrate the existing randomized controlled trials to evaluate the value of 11C-CFT PET combined with 18F-FDG PET in the diagnosis of early PD."( Efficacy of 11C-2β-carbomethoxy-3β-(4-fluorophenyl) tropane positron emission tomography combined with 18F-fluorodeoxyglucose positron emission tomography in the diagnosis of early Parkinson disease: A protocol for systematic review and meta analysis.
Feng, Z; Jiang, L; Li, P; Shao, H; Shi, X; Wang, X, 2020
)
0.56
"Our study may prove that 11C-CFT PET combined with 18F-FDG PET can effectively diagnose early PD."( Efficacy of 11C-2β-carbomethoxy-3β-(4-fluorophenyl) tropane positron emission tomography combined with 18F-fluorodeoxyglucose positron emission tomography in the diagnosis of early Parkinson disease: A protocol for systematic review and meta analysis.
Feng, Z; Jiang, L; Li, P; Shao, H; Shi, X; Wang, X, 2020
)
0.56
" Amyloidosis with diffuse abdominal involvement in combination with pulmonary squamous cell carcinoma carcinoma is an exceptionally rare occurrence."( Lung cancer combined with diffuse peritoneal and mesenteric amyloidosis detected on 18F-FDG PET/CT: A case report.
Song, T; Sun, J; Wang, J; Zhao, B, 2021
)
0.62
"In patients with fever or inflammation of unknown origin (fever of unknown origin [FUO] or inflammation of unknown origin [IUO], respectively), expert consensus recommends the use of positron emission tomography with fluorine-18-fluorodeoxy glucose combined with computed tomography (FDG-PET/CT) when standard work-up fails to identify diagnostic clues."( Predictors of Diagnostic Contributions and Spontaneous Remission of Symptoms Associated with Positron Emission Tomography with Fluorine-18-Fluorodeoxy Glucose Combined with Computed Tomography in Classic Fever or Inflammation of Unknown Origin: a Retrospe
Iwata, M; Terasawa, T; Toyama, H; Tsuzuki, S; Watanabe, A, 2021
)
0.62
"Determine the safety and specificity of a tumor-targeted radiotracer (89Zr-pan) in combination with 18F-FDG PET/CT to improve diagnostic accuracy in head and neck squamous cell carcinoma (HNSCC)."( 89Zr-panitumumab Combined With 18F-FDG PET Improves Detection and Staging of Head and Neck Squamous Cell Carcinoma.
Azevedo, EC; Baik, FM; Castillo, J; Chin, FT; Colevas, AD; Duan, H; Ferri, V; Freeman, L; Hom, M; Iagaru, A; Kaplan, MJ; Koran, ME; Lee, YJ; Martin, BA; Raymundo, RC; Rosenthal, EL; Shen, B; Valencia, A; van den Berg, NS; Zhou, Q, 2022
)
0.72
" In this study, the watershed algorithm (WA) was used to segment the abdominal images to extract images of pancreatic cancer cells and to compare the value of F-FDG PET/CT combined with MRI in the diagnosis of pancreatic occupying lesions."( The Clinical Diagnostic Value of F-FDG PET/CT Combined with MRI in Pancreatic Cancer.
Liu, X; Lu, L; Ren, Y; Wang, J; Yang, X, 2022
)
0.72
" We report here a case diagnosed by positron emission tomography/computed tomography (PET-CT) combined with tumour markers."( Primary small cell carcinoma of the gallbladder diagnosed by PET/CT combined with tumour markers: A case report.
Fu, P; Guo, A; Li, S, 2023
)
0.91

Bioavailability

ExcerptReferenceRelevance
"17), whereas [(18)F]FAc has the highest bioavailability (area under concentration of radiotracer vs."( Biodistribution, pharmacokinetics and PET imaging of [(18)F]FMISO, [(18)F]FDG and [(18)F]FAc in a sarcoma- and inflammation-bearing mouse model.
Chang, CH; Chang, CW; Chang, TJ; Chou, TK; Lin, WJ; Liu, RS; Wang, HE; Wang, SJ; Wu, CY, 2009
)
0.35
"Hypofractionated radiotherapy of rectal cancer leads to an increased tumor perfusion as reflected by an elevated K(trans), possibly improving the bioavailability of cytotoxic agents in rectal tumors, often administered early after radiotherapy treatment."( Tumor perfusion increases during hypofractionated short-course radiotherapy in rectal cancer: sequential perfusion-CT findings.
Aerts, HJ; Backes, WH; Buijsen, J; Janssen, MH; Kierkels, RG; Lambin, P; Lammering, G; Ollers, MC, 2010
)
0.36
" In anesthetized rats, the gastric emptying rate of (18)F-FDG decreased dramatically whereas the intestinal absorption rate constant was not significantly different from that in conscious rats."( PET imaging of the gastrointestinal absorption of orally administered drugs in conscious and anesthetized rats.
Cui, Y; Hayashinaka, E; Kataoka, M; Oh, H; Sakuma, S; Suzuki, N; Takahashi, M; Takashima, T; Wada, Y; Watanabe, Y; Yamashita, S, 2011
)
0.37
" After oral administration of 11C-labeled telmisartan with or without non-radiolabeled telmisartan, systemic bioavailability and hepatic distribution of radioactivity significantly increased non-linearly with dose."( [Dynamic analysis of pharmacokinetics of orally administered drugs using positron emission tomography].
Kataoka, M, 2012
)
0.38
"We aimed to determine whether BAT can be activated in lean and obese humans after acute administration of an orally bioavailable sympathomimetic."( Ephedrine activates brown adipose tissue in lean but not obese humans.
Bertovic, D; Carey, AL; Cherk, MH; Duffy, SJ; Eikelis, N; Formosa, MF; Kalff, V; Kingwell, BA; Lambert, GW; Van Every, B, 2013
)
0.39
" The whole-body average specific absorption rate (SAR) was 4 W/kg for the field of the 915 MHz RFID signal."( The effects of exposure to 915 MHz radiofrequency identification on cerebral glucose metabolism in rat: a [F-18] FDG micro-PET study.
Ahn, YH; An, YS; Choi, HD; Kim, BC; Kim, HS; Kim, N; Lee, YS; Pack, JK; Paik, MJ, 2013
)
0.39
"05), which reduces [(18)F]FDG bioavailability for BAT and other tissues."( Brown adipose tissue activity after a high-calorie meal in humans.
Brans, B; Mottaghy, FM; Schrauwen, P; van Baak, MA; van der Lans, AA; van Marken Lichtenbelt, WD; Vosselman, MJ; Wierts, R, 2013
)
0.39
" Analysis of the PET imaging data revealed that the pharmacokinetic parameters were independent of the dosing solution volume; however, the viscosity increased the absorption rate constant and decreased the mucociliary clearance rate constant."( Visualization of drug translocation in the nasal cavity and pharmacokinetic analysis on nasal drug absorption using positron emission tomography in the rat.
Cui, Y; Furubayashi, T; Hayashi, T; Hayashinaka, E; Irie, S; Katayama, Y; Nakaoka, T; Okauchi, T; Onoe, K; Ose, T; Sakane, T; Shingaki, T; Tanki, N; Wada, Y; Watanabe, Y; Yamaguchi, M, 2016
)
0.43

Dosage Studied

ExcerptRelevanceReference
" Since all patients were scanned while on their current medication regimen, the duration and dosage of the medication of the two patient groups were compared."( Regional metabolism in microsmic patients with schizophrenia.
Clark, C; Hurwitz, T; Kopala, L; Li, D, 1991
)
0.28
"The cognitive-enhancing effects of pramiracetam in animal models of learning and memory are characterized by an inverted U-shaped dose-response curve."( Nootropic drugs in Alzheimer's disease: symptomatic treatment with pramiracetam.
Blin, J; Chase, TN; Claus, JJ; Giuffra, M; Ludwig, C; Mohr, E, 1991
)
0.28
" We measured the standardized uptake value (SUV), a semiquantative evaluation, ROI activity divided by the dosage per weight of each patient."( Monitoring of response to radiotherapy with fluorine-18 deoxyglucose PET of head and neck squamous cell carcinomas.
Kawabe, J; Kitayama, H; Matsuda, M; Nakai, Y; Nasako, Y; Ochi, H; Ohashi, Y; Okamura, T; Sakamoto, H; Sakashita, T, 1998
)
0.3
" The dosage form is the injectable solution (2 ml) containing 185 MBq of 18F-FDG at a calibration time."( [Development of 18F-FDG ([F-18]-2-fluoro-2-deoxy-D-glucose) injection for imaging of tumor reflecting glucose metabolism--results of preclinical studies].
Ino, S; Ito, O; Kanagawa, M; Kato-Azuma, M; Kondo, S; Shimada, T; Shirakami, Y; Suzuki, N, 1999
)
0.3
"To determine the dose-response relationship between the probability of tumor control on the basis of pathologic tumor response (pTCP) and the residual metabolic rate of glucose (MRglc) in response to preoperative chemoradiotherapy in locally advanced non-small-cell lung cancer and to define the level of residual MRglc that corresponds to pTCP 50% and pTCP > or = 95%."( Dose-response relationship between probability of pathologic tumor control and glucose metabolic rate measured with FDG PET after preoperative chemoradiotherapy in locally advanced non-small-cell lung cancer.
Choi, NC; Fidias, P; Fischman, AJ; Lynch, T; Mathisen, D; Niemierko, A; Ryu, JS; Wain, J; Wright, C, 2002
)
0.31
"The correlation between the gradient of residual MRglc after chemoradiotherapy and pTCP is an inverse dose-response relationship."( Dose-response relationship between probability of pathologic tumor control and glucose metabolic rate measured with FDG PET after preoperative chemoradiotherapy in locally advanced non-small-cell lung cancer.
Choi, NC; Fidias, P; Fischman, AJ; Lynch, T; Mathisen, D; Niemierko, A; Ryu, JS; Wain, J; Wright, C, 2002
)
0.31
"A novel microfluidic device was designed and developed to miniaturize, multiplex, and automate serial dilution and three-reagent dose-response assays using submicroliter quantities of reagents."( A prototype microfluidic platform for miniaturization and automation of serial dilution and dose-response assays.
Coyne, C; Flynn, T; Koehler, J; Levine, L; Pezzuto, M; Vajjhala, S; Williams, M, 2002
)
0.31
" However, in the other patient, critical structure dosage from the nonuniform dose prescription exceeded dose-volume/function limits, and greatly exceeded that from the uniform dose prescription."( Feasibility of optimizing the dose distribution in lung tumors using fluorine-18-fluorodeoxyglucose positron emission tomography and single photon emission computed tomography guided dose prescriptions.
Baydush, AH; Bell, M; Craciunescu, O; Das, SK; Dewhirst, MW; Marks, LB; Miften, MM; Munley, MT; Rosenman, JG; Whiddon, CS; Wong, T; Zhou, S, 2004
)
0.32
" From these results, the tumor control probability (TCP) was estimated, assuming a clinical dose-response curve with a median toxic dose of 84."( Increased therapeutic ratio by 18FDG-PET CT planning in patients with clinical CT stage N2-N3M0 non-small-cell lung cancer: a modeling study.
Bentzen, SM; Boersma, L; De Ruysscher, D; Hochstenbag, M; Lambin, P; Lamers, R; Lutgens, L; Nijsten, S; van Der Wel, A; Wanders, R; Wouters, B; Zimny, M, 2005
)
0.33
"Controlling the patient's environmental temperature prior to the dosing and during the uptake phase can significantly reduce FDG uptake in brown fat in the neck and paravertebral areas."( Reduction of brown fat 2-deoxy-2-[F-18]fluoro-D-glucose uptake by controlling environmental temperature prior to positron emission tomography scan.
Acio, E; Atkins, F; Butler, C; Esposito, G; Garcia, CA; Kulkarni, K; Majd, M; Van Nostrand, D,
)
0.13
" We imaged 18 normal volunteers in a dose-escalation study with 3 endotoxin dosing groups (n = 6 in each group): 1 ng/kg, 2 ng/kg, and 4 ng/kg."( FDG-PET imaging of pulmonary inflammation in healthy volunteers after airway instillation of endotoxin.
Chen, DL; Mintun, MA; Rosenbluth, DB; Schuster, DP, 2006
)
0.33
" The mean lamotrigine dosage was 211."( Regional effects of lamotrigine on cerebral glucose metabolism in idiopathic generalized epilepsy.
Hong, SB; Joo, EY; Tae, WS, 2006
)
0.33
" Deviation of the dose-response curve from a linear model was tested."( Radiation pneumonitis: local dose versus [18F]-fluorodeoxyglucose uptake response in irradiated lung.
Ajani, J; Guerrero, T; Hart, J; Johnson, V; Khan, M; Komaki, R; Liao, Z; Luo, D; Pan, T; Stevens, C, 2007
)
0.34
"Because C75 causes an effect that is shorter in duration than expected, modification of the current weekly dosing regimen should be considered."( FDG-PET for pharmacodynamic assessment of the fatty acid synthase inhibitor C75 in an experimental model of lung cancer.
Alvey, S; Gabrielson, E; Gabrielson, K; Hagemann, RL; Kuhajda, FP; Lee, JS; Orita, H; Pomper, MG, 2007
)
0.34
" CT and FDG-related dosage data were gathered from the literature and then extrapolated to the scan parameters at a model PET center."( Cancer screening with whole-body PET/CT for healthy asymptomatic people in Japan: re-evaluation of its test validity and radiation exposure.
Ghotbi, N; Iwanaga, M; Ogawa, Y; Ohtsuru, A; Yamashita, S,
)
0.13
" In addition, we aimed to determine optimum dosing and to determine if there are positron emission tomography (PET)-attenuation effects on 2-deoxy-2[F-18]fluoro-D-glucose (FDG) values due to Fenestra LC."( MicroCT liver contrast agent enhancement over time, dose, and mouse strain.
Stout, DB; Suckow, CE,
)
0.13
"The previously published European Association of Nuclear Medicine (EANM) paediatric dosage card recommends 70 MBq F-18 or F-18 Fluoro-2-Deoxyglucose (F-18-FDG) as the "minimum recommended activity"."( The new EANM paediatric dosage card: additional notes with respect to F-18.
Biassoni, L; Franzius, C; Lassmann, M; Monsieurs, M, 2008
)
0.35
"Mean patient dosage of (18)F-FDG was 699 +/- 181 MBq (range 451-984)."( Comprehensive evaluation of occupational radiation exposure to intraoperative and perioperative personnel from 18F-FDG radioguided surgical procedures.
Hall, NC; Hinkle, GH; Knopp, MV; Marsh, SG; Martin, EW; Povoski, SP; Sarikaya, I; White, WC, 2008
)
0.35
" This protocol is based on standardisation of: (1) patient preparation; (2) matching of scan statistics by prescribing dosage as function of patient weight, scan time per bed position, percentage of bed overlap and image acquisition mode (2D or 3D); (3) matching of image resolution by prescribing reconstruction settings for each type of scanner; (4) matching of data analysis procedure by defining volume of interest methods and SUV calculations and; (5) finally, a multi-centre QC procedure is defined using a 20-cm diameter phantom for verification of scanner calibration and the NEMA NU 2 2001 Image Quality phantom for verification of activity concentration recoveries (i."( The Netherlands protocol for standardisation and quantification of FDG whole body PET studies in multi-centre trials.
Arends, B; Boellaard, R; Comans, EF; Hoekstra, CJ; Hoekstra, OS; Oyen, WJ; Paans, AM; Pruim, J; Verzijlbergen, FJ; Visser, EP; Willemsen, AT; Zijlstra, J, 2008
)
0.35
" This case was deemed in operable, and one-shot bolus of 5-FU was administered through the tumor feeding arteries: the left 3rd, 4th lumbar, and ilio -- lumbar arteries at a dosage of 250 mg/body from each artery."( Arterial infusion chemotherapy in patient with repeated recurrent tumor of cecal cancer: report of a case.
Anazawa, S; Eto, K; Ogawa, M; Takao, Y; Ushigome, T; Watanabe, M; Yamagata, T; Yanaga, K, 2008
)
0.35
" An activation index (AI) was calculated from microPET data o quantify the changes in local metabolic activities normalized to variations in FDG dosage between animals."( MicroPET study of brain neuronal metabolism under electrical and mechanical stimulation of the rat tail.
Chen, YY; Chien, CN; Chou, TW; Jaw, FS; Lee, TW; Shih, YY, 2009
)
0.35
" Consequences are under dosing and thereby possibly ineffective treatment."( Consequences of additional use of PET information for target volume delineation and radiotherapy dose distribution for esophageal cancer.
Beukema, JC; Busz, DM; Langendijk, JA; Muijs, CT; Plukker, JT; Pruim, J; Schreurs, LM; van der Borden, AJ; Van der Jagt, EJ, 2009
)
0.35
" However, IMRT requires a particular attention at the target delineation step to avoid inadequate dosage to TVs/OARs."( [Potential place of FDG-PET for the GTV delineation in head and neck and lung cancers].
Bol, A; Castadot, P; Geets, X; Grégoire, V; Lee, JA, 2009
)
0.35
" Importantly, loss or decrease in PTEN expression was found in all murine MPNSTs and a majority of human NF1-associated MPNST lesions, suggesting that PTEN dosage and its controlled signaling pathways are critical for transformation of NFs to MPNST."( PTEN dosage is essential for neurofibroma development and malignant transformation.
Ao, Y; Dang, J; Dry, SM; Eilber, FC; Gregorian, C; Lawson, G; Liu, X; Mellinghoff, IK; Mischel, PS; Nakashima, J; Nghiemphu, PL; Parada, LF; Phelps, M; Smith, KB; Sofroniew, MV; Wu, H, 2009
)
0.35
"Corticotropin-releasing factor receptor type 1 (CRF(1)) antagonists have been proposed as therapeutic agents in the treatment of mood and anxiety disorders although clinical evidence supporting their development and understanding of a dose-response relationship has been lacking."( Dose-dependent effects of the CRF(1) receptor antagonist R317573 on regional brain activity in healthy male subjects.
Andrews, RD; Brown, T; de Hoon, J; Mannaert, E; Schmidt, ME; Steckler, T; van der Ark, P; Van Laere, K, 2010
)
0.36
" The goal of this study was to investigate the real therapeutic effectiveness of 6 mol% PEG (111)In-vinorelbine liposomes via the elevation of the radiation dosage and reduction in the concentration of chemotherapeutic agents."( Therapeutic efficacy evaluation of 111In-labeled PEGylated liposomal vinorelbine in murine colon carcinoma with multimodalities of molecular imaging.
Chow, TH; Hwang, JJ; Lin, WJ; Lin, YY; Liu, RS; Pang, VF; Ting, G; Tseng, YL; Wang, HE; Yang, CS, 2009
)
0.35
"PET/CT scans obtained at a median of 2 mo after initial dosing did not demonstrate significant changes in lesion size or (18)F-FDG or (18)F-FLT uptake when focusing on metastatic lesions."( Imaging of CTLA4 blockade-induced cell replication with (18)F-FLT PET in patients with advanced melanoma treated with tremelimumab.
Allen-Auerbach, MS; Benz, MR; Chmielowski, B; Czernin, J; Gomez-Navarro, J; McCarthy, T; Radu, C; Ribas, A; Seja, E; Williams, JL, 2010
)
0.36
"[(18)F]FDG uptake was able to reflect the dose-response relationship for cyclophosphamide."( Dose-response relationship in cyclophosphamide-treated B-cell lymphoma xenografts monitored with [18F]FDG PET.
Balzarini, J; Brepoels, L; De Saint-Hubert, M; Mortelmans, L; Mottaghy, FM; Stroobants, S; Verhoef, G, 2010
)
0.36
" This study demonstrated for the first time the use of PET in attaining an IVIVC for a parenterally administered modified release dosage form."( Predicting the in vivo release from a liposomal formulation by IVIVC and non-invasive positron emission tomography imaging.
Bausbacher, N; Buchholz, HG; Hühn, E; Langguth, P; Maus, S; Rösch, F; Schreckenberger, M; Shazly, G; Thews, O, 2010
)
0.36
"The first part (Phase IA) consisted of single day BID dosing every three weeks with consecutive dose escalations."( Clinical Phase I study with an Insulin-like Growth Factor-1 receptor inhibitor: experiences in patients with squamous non-small cell lung carcinoma.
Alvfors, C; Bergman, A; Bergqvist, M; Bergström, S; Dahg, P; Ekman, S; Frödin, JE; Harmenberg, J; Hedlund, A; Ståhl, B, 2011
)
0.37
"We conducted a phase II study to assess the efficacy of continuous dosing of sunitinib in patients with flurodeoxyglucose positron emission tomography (FDG-PET)-avid, iodine-refractory well-differentiated thyroid carcinoma (WDTC) and medullary thyroid cancer (MTC) and to assess for early response per FDG-PET."( Phase II study of daily sunitinib in FDG-PET-positive, iodine-refractory differentiated thyroid cancer and metastatic medullary carcinoma of the thyroid with functional imaging correlation.
Bauman, JE; Capell, PT; Carr, LL; Eaton, KD; Goulart, BH; Kell, EM; Mankoff, DA; Martins, RG, 2010
)
0.36
" On the basis of these results, the recommended Phase II dosage currently being tested is RAD001 70 mg/week in combination with standard chemoradiotherapy."( North Central Cancer Treatment Group Phase I trial N057K of everolimus (RAD001) and temozolomide in combination with radiation therapy in patients with newly diagnosed glioblastoma multiforme.
Brown, PD; Buckner, JC; Galanis, E; Giannini, C; Jaeckle, KA; McGraw, S; Peller, PJ; Sarkaria, JN; Uhm, JH; Wu, W, 2011
)
0.37
" The goal of this retrospective study was to identify the radiation dose-response relationship of parotid gland glucose metabolism in patients with head and neck squamous cell carcinoma (HNSCC)."( FDG-PET assessment of the effect of head and neck radiotherapy on parotid gland glucose metabolism.
Brizel, DM; Hawk, TC; Higgins, KA; Hoang, JK; Roach, MC; Turkington, TG, 2012
)
0.38
" Significant dose-response relationship was observed in SUVmax between group 1 and group 2, and the SUV values gradually decreased from d7 to d14 after treatment."( [Experimental study of CT guided ³²P-CP-PLLA microparticle implantation in the treatment of rabbit VX2 lung tumor].
Huang, P; Liu, L; Pan, D; Wang, L; Xu, Y; Yang, M, 2011
)
0.37
" Pharmacodynamic analysis demonstrated inhibition of IGF-1R phosphorylation in tumors in mice dosed with MEDI-573, indicating that the antitumor activity is mediated via inhibition of IGF-1R signaling pathways."( Dual IGF-I/II-neutralizing antibody MEDI-573 potently inhibits IGF signaling and tumor growth.
Blakey, DC; Bosslet, K; Cartlidge, SA; Chang, YS; Chesebrough, JW; Coats, S; Gao, J; Incognito, L; Jallal, B; Ricketts, SA; Tabrizi, M; Trail, PA; Veldman-Jones, M, 2011
)
0.37
" Each study included in the present review was described in a narrative way, and major components of each study were reported (ie, research design, patient characteristics, types of drugs and radiopharmaceuticals, dosing information and adverse reactions)."( Pitfalls with radiopharmaceuticals.
Machado, M; Santos-Oliveira, R, 2011
)
0.37
"Pediatric (18)F-FDG dosing and acquisition durations are generally based on coarse extrapolation from adult guidelines."( Evaluation of optimal acquisition duration or injected activity for pediatric 18F-FDG PET/CT.
Alessio, AM; Manchanda, V; Mohr, BC; Parisi, MT; Phillips, GS; Sammer, M, 2011
)
0.37
" Serum ACE level was reduced in all cases, and daily steroid dosage was reduced."( Refractory multisystem sarcoidosis responding to infliximab therapy.
Carruthers, D; Croft, AP; Giovanni, G; Gordon, C; Khair, O; Situnayake, D; Sivaguru, A, 2012
)
0.38
" Clinical indices of disease activity, inflammatory markers, and 18Ffluorodeoxyglucose positron emission/computerised tomography findings normalised, while the prednisone dosage could be tapered."( Rescue treatment with tocilizumab for Takayasu arteritis resistant to TNF-α blockers.
Boiardi, L; Catanoso, MG; Dardani, L; Magnani, L; Meliconi, R; Pipitone, N; Pulsatelli, L; Salvarani, C; Versari, A,
)
0.13
" Under the condition of adding 5-FU at various concentrations for 24 hours, the uptake rate of (18)F-FDG was negatively correlated with 5-FU dosage (r = -0."( Early evaluation for treatment efficacy of 5-fluorouracil and hyperthermia on HCT-116 colon cancer cells by fluorine-18-fluorodeoxyglucose uptake.
Chen, SJ; Deng, SM; Wang, ZX; Zhang, B, 2012
)
0.38
"To quantify the post-radiotherapy 2-[(18)F]-fluoro-2-deoxyglucose (FDG) pulmonary uptake dose-response in lung cancer patients and determine its relationship with radiation pneumonitis symptoms."( [18F]-FDG uptake dose-response correlates with radiation pneumonitis in lung cancer patients.
Al Hallack, MN; Castillo, R; Guerrero, T; Lichter, J; Martinez, J; McCurdy, MR; Zouain, N, 2012
)
0.38
"The metabolic radiation pneumonitis dose-response was evaluated from post-treatment FDG-PET/CT imaging."( [18F]-FDG uptake dose-response correlates with radiation pneumonitis in lung cancer patients.
Al Hallack, MN; Castillo, R; Guerrero, T; Lichter, J; Martinez, J; McCurdy, MR; Zouain, N, 2012
)
0.38
" Zolpidem was then given in dosage of 10 mg three times per day."( Zolpidem improves neuropsychiatric symptoms and motor dysfunction in a patient with Parkinson's disease after deep brain stimulation.
Chiou, SM; Hsu, YT; Huang, HY; Kao, CH; Tsai, CH; Tsai, MC; Wu, YC, 2012
)
0.38
" (A Study to Evaluate the Effects of 3 Months Dosing With GW856553, as Assessed FDG-PET/CT Imaging; NCT00633022)."( Effects of p38 mitogen-activated protein kinase inhibition on vascular and systemic inflammation in patients with atherosclerosis.
Cai, G; Cheriyan, J; Choudhury, RP; Collier, DJ; Davies, LC; Davis, B; Elkhawad, M; Fayad, ZA; Gleeson, FV; Lepore, JJ; Marber, MS; Rudd, JH; Sarov-Blat, L; Sprecher, DL; Tawakol, A; Wells, R; Wilkinson, IB; Willette, RN, 2012
)
0.38
" Levetiracetam monotherapy at a dosage of 40 mg/kg/day improved the clinical findings, and seizures were controlled at the end of the first month of treatment."( Acquired epileptiform opercular syndrome: F-18 fluorodeoxyglucose positron emission tomography (FDG-PET) findings and efficacy of levetiracetam therapy.
Akın, R; Arslan, M; Ince, S; Ünay, B; Vurucu, S; Yiş, U, 2012
)
0.38
" A linear dose-response relationship was demonstrated for radioactivity concentrations typical of experiments with rodents."( Blood compatible microfluidic system for pharmacokinetic studies in small animals.
Aimez, V; Baril, FG; Boisselle, V; Charette, PG; Convert, L; Fontaine, R; Lecomte, R; Pratte, JF, 2012
)
0.38
"Glucose metabolic changes in CM patients taking different dosage of analgesic during headache-free periods and clear distinctions in several brain regions were observed."( Overuse of paracetamol caffeine aspirin powders affects cerebral glucose metabolism in chronic migraine patients.
Di, W; Fang, Y; Luo, N; Miao, J; Qi, W; Shi, X; Tao, Y; Xiao, Z; Yi, C; Zhang, A; Zhang, X; Zhu, Y, 2013
)
0.39
"Two mitogen-activated protein kinase kinase (MAPK2, also known as MEK) inhibitors were assessed with (18)F-FDG PET in separate phase I clinical studies, clearly illustrating the potential of metabolic imaging for dose, dosing regimen, and compound selection in early-phase trials and utility for predicting nonresponding patients."( Differences in the biologic activity of 2 novel MEK inhibitors revealed by 18F-FDG PET: analysis of imaging data from 2 phase I trials.
Carlier, T; Chua, S; Gleeson, F; Hugonnet, F; Kraeber-Bodéré, F; Lumbroso, J; Naegelen, VM; Nagarajah, J; Shochat, E; Stokkel, M; Tessier, J; Trampal, C, 2012
)
0.38
" The local dose-response relation was used in the LKB model to calculate the EUD."( Relating acute esophagitis to radiotherapy dose using FDG-PET in concurrent chemo-radiotherapy for locally advanced non-small cell lung cancer.
Belderbos, J; Kwint, M; Lebesque, J; Nijkamp, J; Rossi, M; Sonke, JJ; Uyterlinde, W; van den Heuvel, M; Vogel, W, 2013
)
0.39
" Although sunitinib treatment lowered the patient's blood glucose concentrations further and induced repeated symptomatic hypoglycemic episodes, he was able to tolerate the treatment well after changing the timing of sunitinib dosing and adjusting his diet."( Therapeutic effect of sunitinib malate and its influence on blood glucose concentrations in a patient with metastatic insulinoma.
Chen, J; Cong, L; Cui, Y; Han, J; Luan, Y; Sha, D; Shen, R; Wang, C; Wang, W; Zhang, Z, 2013
)
0.39
" All cross-sectional diagnostic imaging examinations performed for disease assessment after completion of chemotherapy were reviewed and cumulative radiation dosage from these examinations and the frequency of relapse detection by these examinations were recorded."( Pediatric Burkitt's lymphoma and diffuse B-cell lymphoma: are surveillance scans required?
Allen, CE; Bollard, CM; Dreyer, Z; Eissa, HM; Goradia, P; Guillerman, RP; Kamdar, K; McClain, KL; Simko, S; Steuber, P, 2014
)
0.4
"The MTD was 700 mg twice weekly when BIIB021 was dosed for 3 weeks out of each 4-week course."( A phase 1, dose-escalation, pharmacokinetic and pharmacodynamic study of BIIB021 administered orally in patients with advanced solid tumors.
Banerji, U; Castro, J; Lamanna, N; Mita, M; O'Brien, S; Saif, MW; Stogard, C; Takimoto, C; Von Hoff, D, 2014
)
0.4
" The significant dose-response relationship points to the clinical utility of patient-specific absorbed dose calculations for radionuclide therapy."( Quantitative dosimetry for yttrium-90 radionuclide therapy: tumor dose predicts fluorodeoxyglucose positron emission tomography response in hepatic metastatic melanoma.
Barron, B; Eaton, BR; Fox, T; Galt, JR; Kim, HS; Kim, S; Landry, J; Liu, Y; Schreibmann, E; Schuster, DM, 2014
)
0.4
"We evaluated week-on/week-off axitinib dosing plus chemotherapy in patients with gastrointestinal tumours, including tumour thymidine uptake by fluorine-18 3'-deoxy-3'-fluorothymidine positron emission tomography ((18)FLT-PET)."( Intermittent dosing of axitinib combined with chemotherapy is supported by (18)FLT-PET in gastrointestinal tumours.
Bendell, JC; Burris, HA; Hoh, CK; Infante, JR; Kim, S; Reid, TR; Rosbrook, B; Tarazi, J, 2014
)
0.4
") axitinib 7 mg (n=3) or 10 mg (n=18) for 7 days followed by a 7-day dosing interruption; serial (18)FLT-PET scans were performed before day 1 and on days 7, 10, and 14."( Intermittent dosing of axitinib combined with chemotherapy is supported by (18)FLT-PET in gastrointestinal tumours.
Bendell, JC; Burris, HA; Hoh, CK; Infante, JR; Kim, S; Reid, TR; Rosbrook, B; Tarazi, J, 2014
)
0.4
" To compensate for the heterogeneity among multi-institutional patient cohorts and corresponding treatment techniques, local control data of the cohorts were fit to a single dose-response curve with a clinically representative steepness (γ50=2), thereby defining an 'outcome-equivalent dose' (OED) for each institutional cohort."( Estimate of the impact of FDG-avidity on the dose required for head and neck radiotherapy local control.
Deasy, JO; Jeong, J; Lee, NY; Oh, JH; Setton, JS, 2014
)
0.4
"We introduced a novel outcome-equivalent dose analysis method to estimate the dose-response modifying effect of FDG uptake variation."( Estimate of the impact of FDG-avidity on the dose required for head and neck radiotherapy local control.
Deasy, JO; Jeong, J; Lee, NY; Oh, JH; Setton, JS, 2014
)
0.4
" The patient was in need of high dosage of inotrops during the following days."( Detection of necrosis of the gastric fundus after blunt abdominal trauma by PET-CT.
Gabriel, M; Hofer, A; Kratochwill, H; Pentsch, A, 2015
)
0.42
"TAK-733 was administered orally by gavage to nude xenograft rats for 2 weeks, at dosage levels of 0 (0."( Evaluation of the therapeutic efficacy of a MEK inhibitor (TAK-733) using ¹⁸F-fluorodeoxyglucose-positron emission tomography in the human lung xenograft model A549.
Ishino, S; Miyake, H; Mori, I; Vincent, P, 2015
)
0.42
" BMI showed a dose-response association with increased odds (1."(
Aleksunes, LM; Amer, H; Ashare, RL; Avula, RT; Badgaiyan, RD; Bakera, B; Beanlands, R; Bircsak, KM; Blake, J; Blum, K; Braverman, ER; Chakkera, HA; Chandy, G; Chang, CJ; Chang, YH; Chen, CL; Chen, LW; Chiu, CH; Chow, JC; Claupein, W; Contreras-Dominguez, V; D'Aiuto, F; Darbar, U; DaSilva, JN; Davies, RA; deKemp, R; Demotrovics, Z; Denic, A; Dennie, C; Döhler, J; Donath, S; Donos, N; Du, Y; Dunne, R; Dushaj, K; Ehrhart, E; Evans, GC; Gawrońska, H; Giordano, J; Gold, MS; Gruber, S; Hartung, K; Huang, CW; Hubert, S; Johnson, CA; Kolesnichenko, I; Lee, HY; Lerman, LO; Li, M; Lowenthal, DH; Madigan, MA; Makary, T; Mc Ardle, B; Mc Klein, R; McShane, MJ; Mielniczuk, LM; Müller, T; Newton, JM; Nibali, L; Ohira, H; Okoth, EA; Ongarora, BG; Oscar-Berman, M; Palmer, PH; Pekrun, C; Pena, E; Petrie, A; Piepho, HP; Pugliese, C; Rakmanee, T; Renaud, JM; Ritter, DW; Rule, AD; Sakuma, KL; Schoenthaler, SJ; Schulz, R; Smith, KM; Souprountchouk, V; Stewart, DJ; Strasser, AA; Suvan, JE; Thomas, LF; Thompson, B; Tsaur, S; Vicente, MG; Waite, RL; Wang, Q; Wang, X; Wang, YH; Watson, JG; Weiß, K; Wen, X; Xiao, J; Zhou, Z,
)
0.13
"5 %) underwent PSA dosage and biopsy to determine the nature of the incidental uptake."( Multicentre study of 18F-FDG-PET/CT prostate incidental uptake.
Bertagna, F; Bertoli, M; Biasiotto, G; Bosio, G; Dib, B; Fracassi, F; Giovanella, L; Giubbini, R; Piccardo, A; Treglia, G, 2015
)
0.42
"The 2010 North American Consensus Guidelines (NACG) for pediatric administered doses and the European Association of Nuclear Medicine (EANM) Dosage Card guidelines recommend lower activities than those administered at our institution."( Dose Optimization of the Administered Activity in Pediatric Bone Scintigraphy: Validation of the North American Consensus Guidelines.
Ayres, KL; Delbeke, D; Hodges, PK; Martin, WH; Price, R; Spottswood, SE; Wang, L, 2015
)
0.42
" Data were subsampled to represent different administered activities corresponding to the activities recommended by the NACG and the EANM Dosage Card."( Dose Optimization of the Administered Activity in Pediatric Bone Scintigraphy: Validation of the North American Consensus Guidelines.
Ayres, KL; Delbeke, D; Hodges, PK; Martin, WH; Price, R; Spottswood, SE; Wang, L, 2015
)
0.42
"5 mg continuous daily dosing of sunitinib."( FDG and FLT-PET for Early measurement of response to 37.5 mg daily sunitinib therapy in metastatic renal cell carcinoma.
Agarwal, N; Beardmore, B; Boucher, K; Butterfield, RI; Hoffman, JM; Horn, KP; Kadrmas, DJ; Morton, KA; Yap, JT, 2015
)
0.42
" This study's primary objective examined the relationship between GSK2141795, an oral, pan-AKT inhibitor, and (18)F-FDG PET markers of glucose metabolism in tumor tissue to determine whether (18)F-FDG PET could be used to guide personalized dosing of GSK2141795."( Dose-Finding Quantitative 18F-FDG PET Imaging Study with the Oral Pan-AKT Inhibitor GSK2141795 in Patients with Gynecologic Malignancies.
Agarwal, R; Babar, S; Blagden, S; Carme, S; Chen, M; Curry, E; Dina, R; El-Bahrawy, MA; Gabra, H; Gungor, H; Krachey, E; Madison, S; Morris, SR; Pickford, E; Rama, N; Saleem, A; Salinas, C; Santiago-Walker, A; Smith, DA; Stronach, EA, 2015
)
0.42
" No dose-response relationship was observed between GSK2141795 pharmacokinetics and (18)F-FDG PET pharmacodynamic measures; however, an exposure-response relationship was seen between maximum drug concentrations and maximal decrease in (18)F-FDG uptake in the best-responding tumor."( Dose-Finding Quantitative 18F-FDG PET Imaging Study with the Oral Pan-AKT Inhibitor GSK2141795 in Patients with Gynecologic Malignancies.
Agarwal, R; Babar, S; Blagden, S; Carme, S; Chen, M; Curry, E; Dina, R; El-Bahrawy, MA; Gabra, H; Gungor, H; Krachey, E; Madison, S; Morris, SR; Pickford, E; Rama, N; Saleem, A; Salinas, C; Santiago-Walker, A; Smith, DA; Stronach, EA, 2015
)
0.42
" The dosing solution of [(18)F]FDG was varied in volume (ranging from 5 to 25 μl) and viscosity (using 0% to 3% concentrations of hydroxypropylcellulose)."( Visualization of drug translocation in the nasal cavity and pharmacokinetic analysis on nasal drug absorption using positron emission tomography in the rat.
Cui, Y; Furubayashi, T; Hayashi, T; Hayashinaka, E; Irie, S; Katayama, Y; Nakaoka, T; Okauchi, T; Onoe, K; Ose, T; Sakane, T; Shingaki, T; Tanki, N; Wada, Y; Watanabe, Y; Yamaguchi, M, 2016
)
0.43
" We asked whether there is a dose-response relationship between the number of blast-related mild TBIs and uptake of (18)F-fluorodeoxyglucose (FDG), a commonly used indicator of neuronal activity, in the brains of blast-exposed veterans with mild TBI."( Repetitive blast exposure in mice and combat veterans causes persistent cerebellar dysfunction.
Cook, DG; Cross, DJ; Huber, BR; Kraemer, BC; Li, G; Meabon, JS; Meeker, KD; Minoshima, S; Pagulayan, KF; Peskind, ER; Petrie, EC; Raskind, MA; Richards, TL, 2016
)
0.43
" We included the 372 subjects (85 normal subjects, 212 patients with mild cognitive impairment, and 75 patients with AD) with a CSF biomarker dosage (Aβ1-42, t-tau, and p-tau) and brain FDG-PET."( What are the Most Frequently Impaired Markers of Neurodegeneration in ADNI Subjects?
Andriuta, D; Devendeville, A; Godefroy, O; Meyer, ME; Moullart, V; Schraen, S, 2016
)
0.43
" To minimize the acute effects of MPH on FDG uptake, microPET/CT scans were scheduled on Mondays before their first daily dosing of the week (approximately 68h since their last treatment)."( MicroPET/CT assessment of FDG uptake in brain after long-term methylphenidate treatment in nonhuman primates.
Apana, SM; Berridge, MS; Callicott, R; Liu, S; Newport, GD; Paule, MG; Slikker, W; Thompson, J; Wang, C; Zhang, X,
)
0.13
" Normalized uptake may provide patient-specific dose-response information not discernible from dose."( (18)F-Fluorodeoxyglucose Positron Emission Tomography Can Quantify and Predict Esophageal Injury During Radiation Therapy.
Briere, TM; Court, LE; Gomez, DR; Liao, Z; Martel, MK; Mohan, R; Niedzielski, JS; Stingo, F; Yang, J, 2016
)
0.43
" Imaging in two subjects was performed ~4 hr after PET/CT imaging to simulate lower injected F(18-) FDG dose by taking advantage of the natural radioactive decay of the tracer (F(18) half-life of 110 min), with an estimated imaging dosage of 25% of the standard."( Concept of an upright wearable positron emission tomography imager in humans.
Bauer, CE; Brefczynski-Lewis, J; Jaliparthi, G; Lewis, JW; Majewski, S; Mandich, MB; Marano, G; Martone, P; Raylman, RR; Stolin, A, 2016
)
0.43
" Based on this information we derived SUV driven dose-response functions and used these to optimize ideal dose redistributions under the constraint of equal average dose to the tumor volumes as for a conventional treatment."( Dose painting by numbers based on retrospectively determined recurrence probabilities.
Ahnesjö, A; Grönlund, E; Johansson, S; Montelius, A, 2017
)
0.46
" Levothyroxine dosing required doubling in three patients with a known history of hypothyroidism."( Pembrolizumab-Induced Thyroiditis: Comprehensive Clinical Review and Insights Into Underlying Involved Mechanisms.
Bornschlegl, S; Delivanis, DA; Dietz, AB; Gustafson, MP; Kottschade, L; Merten, MM; Ryder, M; Withers, S, 2017
)
0.46
" Incidence of PIs, radiological features, patients' characteristics, underlying NHL type, rituximab/chemotherapy dosing schedules, and symptoms were recorded."( 18F-FDG-PET/CT Pulmonary Infiltrates in Non-Hodgkin Lymphoma Patients Treated with Combined Immunochemotherapy: Incidence and Clinical Characteristics.
Bairey, O; Berger, T; Cohen, YC; Eshel, L; Raanani, P; Shpilberg, O; Stern, D, 2017
)
0.46
" 18F-FDG PET/CT results during treatment induced anti-fungal drugs dosage increase and/or new drugs addition in 8/54 cases (15%) and contributed to the reduction of anti-fungal drugs dosage or treatment withdraws in 17 cases (31%)."( 18F-FDG PET/CT for invasive fungal infection in immunocompromised patients.
Argemi, X; Bund, C; Herbrecht, R; Imperiale, A; Kessler, R; Leroy-Freschini, B; Treglia, G, 2018
)
0.48
" We further demonstrate the importance of precise drug volume dosing to neural structures to elicit behavioral effects reliably."( Focal, remote-controlled, chronic chemical modulation of brain microstructures.
Cima, MJ; Cotler, M; Dagdeviren, C; Graybiel, AM; Joe, P; Langer, R; Nunez-Lopez, C; Ramadi, KB; Rousseau, E; Spencer, KC, 2018
)
0.48
"3years, 48% of patients were successfully weaned from prednisone completely, and 20% were weaned to a maintenance dosage of 5-10mg/d."( Serial Cardiac FDG-PET for the Diagnosis and Therapeutic Guidance of Patients With Cardiac Sarcoidosis.
Fowler, M; Guo, HH; Iagaru, A; Mittra, E; Ning, N; Witteles, R, 2019
)
0.51
" This article describes the current state-of-the-art of the use of FDG-PET/CT for patient selection, prognosis, treatment evaluation, and as a research tool into absorbed dose-response relationships in radioembolization."( The Unique Role of Fluorodeoxyglucose-PET in Radioembolization.
Bastiaannet, R; de Jong, HWAM; Lam, MGEH; Lodge, MA, 2019
)
0.51
" These measures were equivalent to those obtained after 6 days of daily dosing by tofacitinib."( Quantitative tracking of inflammatory activity at the peak and trough plasma levels of tofacitinib, a Janus kinase inhibitor, via in vivo
Abria, C; Chaudhari, AJ; Harmany, ZT; Kundu-Raychaudhuri, S; Raychaudhuri, S; Raychaudhuri, SP; Smith, CM, 2019
)
0.51
" These measures were equivalent to those obtained after 6 days of daily dosing by tofacitinib."( Quantitative tracking of inflammatory activity at the peak and trough plasma levels of tofacitinib, a Janus kinase inhibitor, via in vivo
Abria, C; Chaudhari, AJ; Harmany, ZT; Kundu-Raychaudhuri, S; Raychaudhuri, S; Raychaudhuri, SP; Smith, CM, 2019
)
0.51
" New technologies for automated dosing and infusion delivery are available, however these incorporate both a multidose vial and a multi-patient infusion set."( Use of a radiopharmaceutical multidose dispenser for positron emission tomography: Risk assessment and mitigation measures for infection prevention.
Barton, H; Cheng, A; Karanfilovska, D; Martin, R; Yap, KS, 2020
)
0.56
" However, there is a high rate of locoregional failure in patients with locally advanced non-small cell lung cancer (NSCLC), probably due to the fact that standard dosing may not be effective in all patients."( Radiotherapy Planning and Molecular Imaging in Lung Cancer.
Casali, M; Ciammella, P; Filice, A; Fioroni, F; Galaverni, M; Iotti, C; Versari, A, 2020
)
0.56
"Findings will provide timely information on the safety, efficacy, and optimal dosing of t-PA to treat moderate/severe COVID-19-induced ARDS, which can be rapidly adapted to a phase III trial (NCT04357730; FDA IND 149634)."(
Abbasi, S; Abd El-Wahab, A; Abdallah, M; Abebe, G; Aca-Aca, G; Adama, S; Adefegha, SA; Adidigue-Ndiome, R; Adiseshaiah, P; Adrario, E; Aghajanian, C; Agnese, W; Ahmad, A; Ahmad, I; Ahmed, MFE; Akcay, OF; Akinmoladun, AC; Akutagawa, T; Alakavuklar, MA; Álava-Rabasa, S; Albaladejo-Florín, MJ; Alexandra, AJE; Alfawares, R; Alferiev, IS; Alghamdi, HS; Ali, I; Allard, B; Allen, JD; Almada, E; Alobaid, A; Alonso, GL; Alqahtani, YS; Alqarawi, W; Alsaleh, H; Alyami, BA; Amaral, BPD; Amaro, JT; Amin, SAW; Amodio, E; Amoo, ZA; Andia Biraro, I; Angiolella, L; Anheyer, D; Anlay, DZ; Annex, BH; Antonio-Aguirre, B; Apple, S; Arbuznikov, AV; Arinsoy, T; Armstrong, DK; Ash, S; Aslam, M; Asrie, F; Astur, DC; Atzrodt, J; Au, DW; Aucoin, M; Auerbach, EJ; Azarian, S; Ba, D; Bai, Z; Baisch, PRM; Balkissou, AD; Baltzopoulos, V; Banaszewski, M; Banerjee, S; Bao, Y; Baradwan, A; Barandika, JF; Barger, PM; Barion, MRL; Barrett, CD; Basudan, AM; Baur, LE; Baz-Rodríguez, SA; Beamer, P; Beaulant, A; Becker, DF; Beckers, C; 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Yamamoto, S; Yan, D; Yan, H; Yan, S; Yan, X; Yang, AD; Yang, E; Yang, H; Yang, J; Yang, JL; Yang, K; Yang, M; Yang, P; Yang, Q; Yang, S; Yang, W; Yang, X; Yang, Y; Yao, JC; Yao, WL; Yao, Y; Yaqub, TB; Ye, J; Ye, W; Yen, CW; Yeter, HH; Yin, C; Yip, V; Yong-Yi, J; Yu, HJ; Yu, MF; Yu, S; Yu, W; Yu, WW; Yu, X; Yuan, P; Yuan, Q; Yue, XY; Zaia, AA; Zakhary, SY; Zalwango, F; Zamalloa, A; Zamparo, P; Zampini, IC; Zani, JL; Zeitoun, R; Zeng, N; Zenteno, JC; Zepeda-Palacio, C; Zhai, C; Zhang, B; Zhang, G; Zhang, J; Zhang, K; Zhang, Q; Zhang, R; Zhang, T; Zhang, X; Zhang, Y; Zhang, YY; Zhao, B; Zhao, D; Zhao, G; Zhao, H; Zhao, Q; Zhao, R; Zhao, S; Zhao, T; Zhao, X; Zhao, XA; Zhao, Y; Zhao, Z; Zheng, Z; Zhi-Min, G; Zhou, CL; Zhou, HD; Zhou, J; Zhou, W; Zhou, XQ; Zhou, Z; Zhu, C; Zhu, H; Zhu, L; Zhu, Y; Zitzmann, N; Zou, L; Zou, Y, 2022
)
0.72
" However, to reliably implement this technique, the effect of uncertainties in quantitative PET/CT imaging feedback on tumor voxel dose-response assessment and DPbN needs to be determined and reduced."( Effect of uncertainties in quantitative
Chen, S; Krauss, DJ; Maniawski, P; Qin, A; Wilson, GD; Yan, D, 2020
)
0.56
"Effect of uncertainties in quantitative FDG-PET/CT imaging feedback on intratumoral dose-response quantification was not negligible."( Effect of uncertainties in quantitative
Chen, S; Krauss, DJ; Maniawski, P; Qin, A; Wilson, GD; Yan, D, 2020
)
0.56
" Abatement of arteritis symptoms along with reduction of glucocorticoid dosage was achieved in 12 patients, resulting in a remission induction rate of 70."( Evaluation of tocilizumab for intractable Takayasu arteritis and
Isobe, M; Maejima, Y; Saji, M; Tateishi, U, 2021
)
0.62
" Responder analysis definitions were based on; dosage of immunosuppressive drugs, improvement in functional class, left ventricular ejection fraction (LVEF) and SUVmax."( Effectiveness and safety of infliximab in cardiac Sarcoidosis.
Akdim, F; Azzahhafi, J; Bakker, ALM; Grutters, JC; Keijsers, RGM; Mathijssen, H; Post, MC; Swaans, MJ; Veltkamp, M, 2021
)
0.62
"In analogy to the existing EANM dosage card, new parameters for the EANM paediatric dosage card were developed (class B, baseline value: 10."( The effect of modern PET technology and techniques on the EANM paediatric dosage card.
Dickson, J; Eberlein, U; Lassmann, M, 2022
)
0.72
"With this, recommendations for paediatric dosing are given for systems that have not been considered previously."( The effect of modern PET technology and techniques on the EANM paediatric dosage card.
Dickson, J; Eberlein, U; Lassmann, M, 2022
)
0.72
" A dose-response curve was generated by binning each voxel in the heart into 10 Gy dose-bins and analyzing the SUVmean changes in each dose-bin."( Cardiac metabolic changes on
Castillo, E; Castillo, R; Goodman, KA; Jones, B; Miften, M; Olsen, J; Schefter, T; Vinogradskiy, Y; Zakem, SJ, 2023
)
0.91
" A titration dosing regimen of thionamide anti-thyroid drug (ATD) was used to establish euthyroidism over 12-24 weeks."( Brown adipose tissue influences adiponectin and thyroid hormone changes during Graves' disease therapy.
Goh, HJ; Ho, WE; Leow, MKS; Sun, L; Tint, MT, 2022
)
0.72
" However, statin dosage was significantly associated with Aβ deposition in 2 years (r = -0."( Does statin use affect amyloid beta deposition and brain metabolism?
Balabandian, M; Nabizadeh, F; Valizadeh, P, 2023
)
0.91
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (2)

ClassDescription
2-deoxy-2-fluoro-aldehydo-D-glucose
2-deoxy-2-((18)F)fluoro-D-glucose
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Bioassays (8)

Assay IDTitleYearJournalArticle
AID609650Cellular uptake in mouse S180 cells after 30 mins2011Bioorganic & medicinal chemistry letters, Aug-15, Volume: 21, Issue:16
Synthesis and biological evaluation of novel F-18 labeled pyrazolo[1,5-a]pyrimidine derivatives: potential PET imaging agents for tumor detection.
AID609652Cellular uptake in mouse S180 cells after 60 mins2011Bioorganic & medicinal chemistry letters, Aug-15, Volume: 21, Issue:16
Synthesis and biological evaluation of novel F-18 labeled pyrazolo[1,5-a]pyrimidine derivatives: potential PET imaging agents for tumor detection.
AID335928Decrease in urinary excretion of thromboxane B2 in adenine rich diet fed LWH:Wistar rat at 10 mg/g, ip administered from day 7 to day 12 of adenine ingestion
AID335930Increase in urinary excretion of prostaglandin E2 in adenine rich diet fed LWH:Wistar rat at 10 mg/g, ip administered from day 7 to day 12 of adenine ingestion
AID335929Protection against renal failure in adenine rich diet fed LWH:Wistar rat up to 20 mg/g, ip administered once daily from day 7 to day 12 of adenine ingestion
AID335927Effect on urinary excretion of prostaglandin in adenine rich diet fed LWH:Wistar rat assessed as urine TXB2 level per 24 hrs at 10 mg/g, ip administered from day 7 to day 12 of adenine ingestion
AID335925Effect on urinary excretion of prostaglandin in adenine rich diet fed LWH:Wistar rat assessed as urine prostaglandin E2 level per 24 hrs at 10 mg/g, ip administered from day 7 to day 12 of adenine ingestion
AID335926Effect on urinary excretion of prostaglandin in adenine rich diet fed LWH:Wistar rat assessed as urine 6-keto-PGF1-alpha level per 24 hrs at 10 mg/g, ip administered from day 7 to day 12 of adenine ingestion
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (32,596)

TimeframeStudies, This Drug (%)All Drugs %
pre-1990461 (1.41)18.7374
1990's2183 (6.70)18.2507
2000's8459 (25.95)29.6817
2010's15697 (48.16)24.3611
2020's5796 (17.78)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 52.35

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index52.35 (24.57)
Research Supply Index10.52 (2.92)
Research Growth Index5.42 (4.65)
Search Engine Demand Index92.59 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (52.35)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials2,160 (6.21%)5.53%
Trials0 (0.00%)5.53%
Reviews3,791 (10.90%)6.00%
Reviews0 (0.00%)6.00%
Case Studies7,933 (22.81%)4.05%
Case Studies0 (0.00%)4.05%
Observational246 (0.71%)0.25%
Observational0 (0.00%)0.25%
Other20,641 (59.36%)84.16%
Other6 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Clinical Trials (407)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
A Phase II Study of Neoadjuvant Cisplatin and Gemcitabine Plus Sorafenib for Patients With Transitional-Cell Carcinoma of the Bladder [NCT01222676]Phase 245 participants (Anticipated)Interventional2010-10-31Recruiting
Impact of Local Tissue Inflammation on Intramyocardial Conduction Pathways Post Percutaneous Valve : Evaluation by Positron Emission Tomography on Exploratory Cohort [NCT05308888]Phase 2100 participants (Anticipated)Interventional2022-05-01Not yet recruiting
Endoprosthesis Treatment Effects on Human Abdominal Aorta Aneurysms(AAA)Metabolic Activity [NCT01253252]45 participants (Actual)Interventional2009-08-31Completed
A Randomized Phase 3 Trial of Continuous vs. Intermittent Maintenance Therapy With Zanubrutinib as Upfront Treatment in Older Patients With Mantle Cell Lymphoma [NCT05976763]Phase 3421 participants (Anticipated)Interventional2023-09-08Recruiting
PET fUnCtionaL Imaging to Evaluate Cardiac Radiation Damage (EUCLID) [NCT05775939]20 participants (Anticipated)Interventional2023-01-20Recruiting
A Phase 1/2 Study of Tiragolumab (NSC# 827799) and Atezolizumab (NSC# 783608) in Patients With Relapsed or Refractory SMARCB1 or SMARCA4 Deficient Tumors [NCT05286801]Phase 1/Phase 286 participants (Anticipated)Interventional2022-11-17Recruiting
Phase I Dose-Escalation Bioavailability Study of Oral Triapine in Combination With Concurrent Chemoradiation for Locally Advanced Cervical Cancer (LACC) and Vaginal Cancer [NCT02595879]Phase 122 participants (Actual)Interventional2019-09-18Active, not recruiting
A Pilot Prospective Study of the RefleXion [18F]- FDG PET-CT Subsystem Imaging Performance in Patients With Various Malignancies [NCT05844306]20 participants (Anticipated)Interventional2023-03-15Recruiting
A Phase I Dose Escalation Trial: Concurrent Intensity-Modulated Radiotherapy (IMRT) and Chemotherapy With Molecular Image-Guided Adaptive Radiation Therapy (IGART) for Advanced Head and Neck Squamous Cell Carcinomas (HNSCC) [NCT01283178]Phase 13 participants (Actual)Interventional2011-07-31Terminated(stopped due to The study was terminated. The data analysis was futile with only 3 accruals. PI opted to terminate with IRB and withdraw FDA IND.)
A Phase I Study of Preoperative Chemoradiation With Oxaliplatin, 5-Fluorouracil, Erlotinib and Radiation Followed by Resection and Consolidative Erlotinib for Patients With Locally Advanced Cancer of the Esophagus and Gastroesophageal Junction [NCT01561014]Phase 19 participants (Actual)Interventional2007-04-30Completed
Phase I/II Study of High Dose Interleukin 2, Aldesleukin, in Combination With the Histone Deacetylase Inhibitor Entinostat in Patients With Metastatic Renal Cell Carcinoma [NCT01038778]Phase 1/Phase 247 participants (Actual)Interventional2009-10-29Active, not recruiting
Comparaison Entre la Performance du 18F-FDG PET/CT et de la Scintigraphie Osseuse/Gallium ou de la Scintigraphie Osseuse/Globules Blancs marqués /Souffre colloïdal Dans le Diagnostic d'Une ostéomyélite du Pied ou de la Cheville [NCT03712046]2 participants (Actual)Interventional2019-01-15Terminated(stopped due to Poor patient recruitment)
Tumor Angiogenesis in Non-Small Cell Lung (NSCLC), Colorectal, Breast, Esophageal, Head and Neck Cancer: Radiology-Pathology and Prognostic Correlation [NCT01254591]500 participants (Anticipated)Interventional2006-11-30Recruiting
The Role of Positron Emission Tomography (PET) Imaging in the Evaluation of Response to Sorafenib Treatment in Advanced Hepatocellular Carcinoma. [NCT01157013]40 participants (Actual)Interventional2009-01-31Completed
A Study to Assess the Impact of Moderate/Significant Infiltrations on the Standardized Uptake Values of Target Lesions [NCT03320564]2 participants (Actual)Interventional2018-08-27Terminated(stopped due to Recruitment slow due to improved extravasation rate.)
Role of Dedicated Breast PET in the Characterisation of Indeterminate Breast Lesions on MRI Requiring a Second-look Ultrasound - a Feasibility Study [NCT03198442]12 participants (Actual)Interventional2016-10-05Completed
Phase I Dose-Escalation Study of BCMA/CS1 Bispecific Chimeric Antigen Receptor (CAR)-T Cells for Relapsed/Refractory Multiple Myeloma [NCT05950113]Phase 130 participants (Anticipated)Interventional2024-03-28Not yet recruiting
18F-DCFPyL PET/CT in Hepatocellular Carcinoma [NCT05009979]Phase 250 participants (Anticipated)Interventional2023-01-18Recruiting
Non-alcoholic Fatty Liver Disease Parametric PET (FLiPP) Study [NCT02754037]120 participants (Anticipated)Observational2016-04-30Active, not recruiting
EVALUATION OF THE DIAGNOSTIC VALUE OF PET (18F-FDG) IN CHRONIC GRAFT VERSUS HOST DISEASE (cGVH) [NCT02352064]26 participants (Anticipated)Interventional2015-01-31Recruiting
An Adaptive Design Open Label Pilot Study in Rheumatoid Arthritis Patients to Assess Inflammation Using Molecular Imaging Techniques [NCT02350426]Phase 110 participants (Actual)Interventional2015-08-12Terminated(stopped due to A decision to stop the study was made by the site and GSK project team based on pre-defined stopping criteria in the protocol)
18F-FSPG PET/CT and Integrated Biomarkers for Early Lung Cancer Detection in Patients With Indeterminate Pulmonary Nodules [NCT03824535]Phase 250 participants (Anticipated)Interventional2019-02-04Recruiting
Open Label Randomized Trial of Early Assessment of Therapy Response Using 18FDG-PET/CT in Patients With Marginally Resectable Stage IIIA (N2) Non-Small Cell Lung Cancer (NSCLC) Treated With Induction Concurrent Chemoradiation Followed by Resection and Adj [NCT01314677]0 participants (Actual)Interventional2011-04-30Withdrawn(stopped due to No subjects have been accrued to this trial. The PI will no longer be at COH and requests a study withdrawal/closure.)
NY-ESO-1 TCR Engineered Adoptive Cell Transfer Therapy With CTLA4 Blockade [NCT02070406]Phase 14 participants (Actual)Interventional2014-07-17Terminated(stopped due to low accrual)
Study of the Cerebral Metabolism in Patients With Refractory Chronic Cluster Headache Treated by Occipital Nerve Stimulation [NCT02081482]20 participants (Actual)Interventional2014-03-31Active, not recruiting
Brown Adipose Tissue Activity Young and Older Individuals [NCT02130154]16 participants (Actual)Observational2013-05-31Completed
A Phase III, Multi-center, Single-blind, Cross-over Study to Evaluate the Efficacy and Safety of 18Ffluorocholine (18F-FCH) Comparing With 18F-fluorodeoxyglucose (18F-FDG) for Detecting Hepatocellular Carcinoma [NCT02074202]Phase 3150 participants (Anticipated)Interventional2014-02-28Not yet recruiting
Comparison of PET/CT vs. PET/MRI [NCT03125629]Phase 253 participants (Actual)Interventional2014-05-27Completed
Improving PET Image Quality and Quantification by Using Motion Correction, Parametric Imaging and MAP Reconstruction [NCT04417998]Phase 470 participants (Anticipated)Interventional2020-06-03Enrolling by invitation
Cohort Study Evaluating 18FDG PET for Early Identification of Tumor Exhaust for Immunotherapy in Patients With Locally Advanced or Metastatic Non-Small Cell Bronchopulmonary Carcinoma or Melanoma [NCT03584334]100 participants (Anticipated)Interventional2019-04-04Recruiting
Per-operating Use of a Probe for Detection of β+ [NCT02666599]60 participants (Anticipated)Interventional2014-02-28Recruiting
Molecular Imaging in Infective Endocarditis Using Hybrid Positron Emission Tomography/Magnetic Resonance Imaging (PET/MR) and Computed Tomography (PET/CT) [NCT03626571]60 participants (Anticipated)Observational2018-05-01Recruiting
Early Metabolic Response Evaluation With 18-FDG PET-CT in Esophageal Cancer Treated With Neoadjuvant Chemoradiotherapy Followed by Esophagectomy [NCT01269970]0 participants Observational2004-01-31Completed
Assessment of Response Before, During and After Neoadjuvant Chemoradiotherapy in Rectal Cancer Patients [NCT01171300]94 participants (Actual)Interventional2010-10-31Active, not recruiting
Phase II Study of Bevacizumab Plus Irinotecan (Camptosar™) in Children With Recurrent, Progressive, or Refractory Malignant Gliomas, Diffuse/Intrinsic Brain Stem Gliomas, Medulloblastomas, Ependymomas and Low Grade Gliomas [NCT00381797]Phase 297 participants (Actual)Interventional2006-08-31Completed
Diagnostic Performance of PET/MRI Versus Standard of Care Imaging (PET/CT and/or CT and/or PET) in Preoperative Women With Presumed Early-stage High Grade Endometrial Carcinoma [NCT05390021]33 participants (Anticipated)Interventional2023-03-30Not yet recruiting
Risk of Developing Dementia and Associated Factors in Patients With Normal Brain FDG PET [NCT04804722]100 participants (Actual)Observational2022-01-20Completed
Radiotherapy Dose De-escalation in HPV-Associated Cancers of the Oropharynx Using Metabolic Signature From Interim 18FDG-PET/CT [NCT04667585]120 participants (Anticipated)Interventional2021-04-12Recruiting
Positron Lymphography Via Intracervical 18F-FDG Injection for Pre-surgical Lymphatic Mapping in Stage IB1 Cervical Cancer and High-grade Endometrial Cancer [NCT02285192]Phase 142 participants (Actual)Interventional2014-11-30Active, not recruiting
A Pilot Study to Evaluate the Utility of Interim Digital PET/CT in Predicting Outcomes for Locally Advanced Oropharyngeal Cancer [NCT04140513]25 participants (Anticipated)Interventional2020-10-09Suspended(stopped due to PI decision)
Open-label, Multicenter Study of the 18F-labeled PET/CT (Positron Emission Tomography / Computed Tomography) Tracer BAY86-9596 Following a Single Intravenous Administration of 200 or 300 MBq (Corresponding to ≤ 18 µg Mass Dose) for Evaluation of Radiation [NCT01089998]Phase 135 participants (Actual)Interventional2010-05-31Completed
Brown Adipose Tissue Activity and Energy Metabolism in Cachexia Induced by Cancer or Chronic Disease [NCT02500004]16 participants (Actual)Interventional2015-06-30Completed
Pilot Safety and Feasibility Study of an In Vivo Sensitivity Screen Using a Direct Tumor Microinjection Technique and FDG-PET [NCT03432741]Phase 139 participants (Anticipated)Interventional2018-03-27Suspended(stopped due to funding - sponsor filing of Chapter 11 bankruptcy)
Alterations in the Brain's Connectome in Severe Traumatic Brain Injury [NCT02424656]35 participants (Actual)Observational2014-09-30Completed
Dual 64Cu-DOTATATE and 18F-FDG PET/CT Imaging of Patients With Neuroendocrine Neoplasms [NCT05709171]Phase 2200 participants (Anticipated)Interventional2023-01-17Enrolling by invitation
PET/CT Characterization of Treatment Resistance of AR-targeted Therapies in mCRPC [NCT05647564]20 participants (Anticipated)Interventional2023-03-06Recruiting
Phase IIa Clinical Trial: Feasibility Study on Non-Invasive Simultaneous Hyperpolarized [1-13C]Pyruvate Magnetic Resonance Spectroscopy and 18F-FDG PET (hyperPET) for Metabolic Imaging in Patients With Cancer [NCT05396118]Phase 215 participants (Anticipated)Interventional2022-05-18Enrolling by invitation
A Phase 3 Randomized Trial for Patients With De Novo AML Comparing Standard Therapy Including Gemtuzumab Ozogamicin (GO) to CPX-351 With GO, and the Addition of the FLT3 Inhibitor Gilteritinib for Patients With FLT3 Mutations [NCT04293562]Phase 31,400 participants (Anticipated)Interventional2020-07-21Recruiting
Pilot Study of a Breast-Dedicated PET Camera With 1 Millimeter Spatial Resolution [NCT04016818]Early Phase 120 participants (Anticipated)Interventional2023-01-31Not yet recruiting
A Prospective Study on Comparison 18F-FAPI and 18F-FDG PET/CT in the Evaluation of Patients With Various Types of Cancer [NCT05485792]200 participants (Anticipated)Interventional2022-08-01Not yet recruiting
"Combined One Stop Shop NaF/FDG PET/MRI Evaluation of Response to Xofigo® in mCRPC Patients: A Pilot Study" [NCT02429804]Phase 14 participants (Actual)Interventional2015-04-30Terminated(stopped due to Accrual factor)
A Pilot Study of 18F-FDG PET-CT Kinetic Analysis in Head and Neck Squamous Cell Carcinoma (HNSCC) [NCT02678884]20 participants (Anticipated)Interventional2014-10-31Recruiting
[18 F]-Fluorodeoxyglucose (18F-FDG) Positron Emission Tomography (PET) in Cardiac Sarcoidosis [NCT01764191]0 participants Expanded AccessApproved for marketing
Contribution of 18F-FDG PET-CT in the Diagnosis and the Detection of Peripheral Emboli of Infectious Endocarditis on Native Valves [NCT03695861]31 participants (Actual)Interventional2018-11-10Completed
Development of Radiation Free Whole Body MR Imaging Technique for Staging of Children With Cancer. [NCT01542879]Phase 1/Phase 275 participants (Anticipated)Interventional2012-02-29Recruiting
Could Positon Emission Tomography With Radiolabelled 3'-Deoxy-3'-(18)F-Fluoro-L-Thymidine be a Theranostic Tool During Erlotinib Treatment in Non-small Cell Lung Cancer Patients ? [NCT02069418]Phase 280 participants (Anticipated)Interventional2014-02-28Active, not recruiting
Evaluation of Resectable Cervical Carcinoma With PET/MRI [NCT04219904]Early Phase 125 participants (Anticipated)Interventional2018-09-07Active, not recruiting
Pilot Study of Gene Expression and FDG-PET/MR Biomarkers for Evaluation of Response to Neoadjuvant Therapy for Locally Advanced Rectal Cancer [NCT02112162]Phase 12 participants (Actual)Interventional2014-06-30Terminated(stopped due to Loss of funding)
18F-FAPI PET/CT and 18F-FDG PET/CT in Patients With Pancreatic Adenocarcinoma : A Prospective, Single-Center, Comparative Study [NCT05884463]62 participants (Actual)Interventional2021-04-01Completed
PET/CT Guided Antifungal Stewardship in Invasive Pulmonary Aspergillosis [NCT02955966]51 participants (Actual)Interventional2017-06-02Completed
Evaluation of the Diagnostic and Prognostic Role of PET (PET/CT and PET/MRI) in Gynecological Tumors. [NCT06159907]380 participants (Anticipated)Observational2021-10-27Recruiting
Exploratory Evaluation of Simultaneous Cardiac PET/MR, Metabolomic Markers and Circulating DNA as Possible Prognostic Markers in Identifying Patients Developing Transient or Permanent Cardiopulmonary Dysfunctions After Radiotherapy [NCT04901884]40 participants (Anticipated)Interventional2021-06-01Recruiting
Arterial Imaging of Inflammation and Resolution After Endovascular Surgery [NCT03590769]Phase 19 participants (Actual)Interventional2017-06-01Completed
Diagnostic Accuracy of Positron Emission Tomography/ Computed Tomography With 18F-fluoro-2-deoxyglucose (18F- FDG PET/CT) in Patients With Colorectal Cancer [NCT03572595]45 participants (Anticipated)Observational2018-07-01Not yet recruiting
Positron Emission Tomography Assessment of Acute Lung Transplant Rejection [NCT02204202]28 participants (Actual)Observational2014-02-28Terminated(stopped due to PI left institution)
Evaluating Fluorine-18 Fluorodeoxyglucose Positron Emission Tomography /Computed Tomography With Liver SUVmax-based Criteria for Prognosis of Patients With Peripheral T-cell Lymphoma [NCT03051568]80 participants (Anticipated)Interventional2017-03-01Not yet recruiting
18FDG-PET/MRI Imaging in Predicting Pathological Response to Neo-adjuvant Chemo-Radiotherapy in Rectal Cancer [NCT06057831]Phase 240 participants (Anticipated)Interventional2024-05-31Not yet recruiting
Nectin-4 Targeting ADC Probe for PET Imaging in Solid Tumors [NCT05322512]20 participants (Anticipated)Interventional2024-05-01Not yet recruiting
Characterization in 18F-FDG PET-CT of Brain and Lung Lesions in Young Subjects With Sequelae Psycho-cognitive Disorders in the Aftermath of Severe Covid-19 [NCT04764721]25 participants (Actual)Interventional2021-11-17Completed
18F-DCFPyL PET/CT in High Risk and Recurrent Prostate Cancer [NCT03181867]Phase 2330 participants (Anticipated)Interventional2017-08-03Enrolling by invitation
Molecular Imaging Visualization of Tumor Heterogeneity in Non-small Cell Lung Cancer [NCT04553601]150 participants (Anticipated)Interventional2019-10-01Recruiting
Surveillance With PET/CT and Liquid Biopsies of Stage I-III Lung Cancer Patients After Completion of Definitive Therapy; a Randomized Controlled Trial [NCT03740126]750 participants (Actual)Interventional2018-10-25Active, not recruiting
Characterizing Histiocytosis With 68Ga-FAPI PET/CT [NCT05803629]100 participants (Anticipated)Interventional2023-05-01Not yet recruiting
Biological Interconnection of Brain Neurobiological Activity With Atherosclerotic Plaque Vulnerability and the Prognostic Value [NCT05545618]300 participants (Anticipated)Observational2015-01-01Recruiting
Tumor Perfusion and Hypoxia Evaluation and Comparation in 18F-FDG PET/CT [NCT03373994]40 participants (Anticipated)Observational2016-11-01Recruiting
Relation of Carotid Artery Plaque Inflammation, Covert Stroke and White Matter Disease [NCT01236508]Phase 450 participants (Anticipated)Interventional2010-11-30Terminated(stopped due to difficulties recruiting this population for study population)
Activation of Brown Adipose Tissue in Lean and Obese Men [NCT02173834]20 participants (Actual)Interventional2013-03-31Completed
The Role of Nuclear Imaging in Heart Failure: Correlation With Cardiac Function and Metabolism, Biomarkers and Clinical Prognosis [NCT02697669]200 participants (Anticipated)Observational2012-08-31Recruiting
Pilot Study of Allogeneic/Syngeneic Blood Stem Cell Transplantation in Patients With High-Risk and Recurrent Pediatric Sarcomas [NCT00043979]Phase 260 participants (Actual)Interventional2002-09-19Completed
A Phase Ib/II Study of AZD2171 in Combination With Daily Temozolomide and Radiation in Patients With Newly Diagnosed Glioblastoma Not Taking Enzyme-Inducing Anti-epileptic Drugs [NCT00662506]Phase 1/Phase 246 participants (Actual)Interventional2008-04-30Completed
Comparison of FDG and FAPI in Patients With Various Types of Cancer [NCT04416165]3,000 participants (Anticipated)Interventional2019-10-20Recruiting
Effect of 18-FDG PET/CT Imaging on Clinical Decision Making During the Acute Phase of Infective Endocarditis: a Multicenter Prospective Impact Study [NCT02287792]150 participants (Actual)Interventional2015-04-17Completed
A Cancer Research UK Phase I Trial to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Aurora B Inhibitor GSK1070916A in Patients With Advanced Solid Tumors [NCT01118611]Phase 138 participants (Actual)Interventional2010-03-31Completed
PET Imaging of Hemophilic Arthropathy Correlates With Clinical, Radiographic and Sonographic Assessments [NCT03485170]20 participants (Actual)Interventional2018-01-22Completed
Investigating the Role of Audiovisual Biofeedback on Image Quality During 4D Anatomic and Functional Imaging [NCT01172041]10 participants (Actual)Observational2010-07-31Completed
Comparison of F-18 FDG PET CT and PET MRI With C-11 Acetate PET CT and PET MRI in the Diagnosis of Active Multiple Myeloma Disease: a Pilot Study [NCT03262389]Phase 210 participants (Actual)Interventional2017-09-19Completed
18F-Fluorodeoxyglucose Positron Emission Tomography in Oncology and Neurology [NCT01180751]Phase 31,000 participants (Anticipated)Interventional2010-07-31Enrolling by invitation
[NCT02510872]19 participants (Actual)Interventional2011-12-31Completed
[NCT01322477]25 participants ObservationalNot yet recruiting
Development of Activity MRI (aMRI): Direct Comparison to PET in Human Subjects [NCT05937776]20 participants (Anticipated)Observational2023-12-11Not yet recruiting
Ideal Imaging Time Point Assessment for Spinal Cord Lesions of Unknown Etiology With FDG PET-MRI [NCT04219969]20 participants (Anticipated)Interventional2018-09-21Active, not recruiting
A Sub-study of 18F-DCFPyL Positron Emission Tomography / Computed Tomography (PET/CT) for Assessment of Recurrent Prostate Cancer Evaluation of the Safety and Sensitivity of 68Ga-DOTATOC PET/CT for Imaging NET Patients [NCT04017104]60 participants (Anticipated)Observational2019-11-01Recruiting
Comparison of FLT and FDG PET in the Evaluation of Response to Cetuximab, Cisplatin and Radiation Therapy in Advanced Head and Neck Malignancies or Response to Standard Chemo-radiotherapy in Esophageal Malignancies [NCT00757549]Early Phase 130 participants (Anticipated)Interventional2008-09-30Completed
A Pilot Study of FDG-PET Variability to Establish Biology-Guided Treatment Planning Feasibility for Stereotactic Body Radiation Therapy [NCT03493789]Phase 119 participants (Actual)Interventional2018-04-13Completed
68Ga-FAPI-LM3 PET/CT Imaging in Patients With FAP/SSTR2 Positive Disease and Compared With 18F-FDG [NCT05873777]30 participants (Anticipated)Interventional2023-04-09Recruiting
Relationship Between Histopathological Features, Mutation Status, 18F-FDG PET/CT Radiomic Imaging Parameters as Well as Clinical Outcome in Patients With Treatment-naïve Non-small Cell Lung Cancer [NCT04276025]2,000 participants (Actual)Observational2016-07-31Completed
A Pilot Study Treatment of Malignant Tumors Using [18F] Fluorodeoxyglucose (FDG) [NCT02130492]Phase 1/Phase 24 participants (Actual)Interventional2014-05-31Suspended(stopped due to Temporarily interrupted due to lack of funding: will re-open in the near future)
Combined 18F-NaF/18F-FDG PET/MRI for Detection of Skeletal Metastases [NCT00375830]Phase 2114 participants (Actual)Interventional2006-01-31Completed
A Comparison of NETSPOT Imaging Versus F-FDG-PET in Head and Neck Cancer Patients [NCT03602911]Phase 230 participants (Anticipated)Interventional2019-02-01Recruiting
Improving Breast Cancer Staging With 18F-FDG PET/CT Imaging (The IMBRECAS PET Study) [NCT05730608]300 participants (Anticipated)Interventional2023-02-16Recruiting
Diagnostic Potential of PET/MRI in Cardiac Sarcoidosis: A Pilot Study Combining Advanced MRI and 18F-FDG and 18F-GE180 PET of the Myocardium [NCT03561025]33 participants (Actual)Interventional2018-10-01Completed
Prospective Comparison of 18F-choline PET/CT and 18F-FDG PET/CT in the Initial Work-up of Multiple Myeloma [NCT03891914]Phase 330 participants (Anticipated)Interventional2019-11-12Recruiting
18F-AlF-FAPi-04 PET/CT Imaging in Patients With Solid Tumor [NCT06126705]Early Phase 160 participants (Anticipated)Interventional2023-07-18Recruiting
18F-FDG PET Scan and MRI Diffusion : Correlation Study of the Evaluation of the Early Therapeutic Response of Diffuse Large B-cell Lymphoma [NCT03121456]74 participants (Anticipated)Interventional2017-10-13Active, not recruiting
Evaluation of Right Ventricular Function and Metabolism Following Riociguat for the Treatment of Chronic Thromboembolic Pulmonary Hypertension- Images of Rio [NCT02094001]Phase 26 participants (Actual)Interventional2014-05-31Completed
Pilot Study of PET-CT Imaging Using FDG-labeled Human Erythrocytes in Breast Cancer Patient Before and After Neoadjuvant Chemotherapy [NCT03295695]Early Phase 10 participants (Actual)Interventional2020-12-31Withdrawn(stopped due to closure of radiolaboratory)
A Prospective Exploration in the Clinical Value of 68Ga-DOTANOC PET/CT and 18F-FDG PET/CT in Neuroendocrine Neoplasms [NCT03288597]146 participants (Anticipated)Observational [Patient Registry]2017-09-01Recruiting
Pilot PET Imaging Study of [89Zr]DFO-YS5 for Detecting CD46 Positive Malignancy in Multiple Myeloma [NCT05892393]Phase 120 participants (Anticipated)Interventional2023-06-16Recruiting
Diffusion-weighted MRI for Individualized Radiation Therapy Planning of Lung Cancer [NCT02059889]0 participants (Actual)Interventional2014-07-31Withdrawn(stopped due to slow accrual)
Biokinetics Study for F-18 FDG for Dose Reduction in Pediatric Molecular Imaging [NCT03107325]Phase 40 participants (Actual)Interventional2019-02-01Withdrawn(stopped due to No subjects who met the study criteria agreed to participate in two years prior to the COVID-19 crisis.)
Evaluating Fluorine-18 Fluorodeoxyglucose Positron Emission Tomography / Computed Tomography With Liver SUVmax-based Criteria for Prognosis of Patients With NK/T-cell Lymphoma [NCT03051542]60 participants (Anticipated)Interventional2017-03-01Not yet recruiting
68Ga-RM26-RGD PET/CT Imaging in the GRPR and αvβ3 Positive Tumor Patients [NCT05549024]Early Phase 190 participants (Anticipated)Interventional2022-08-16Recruiting
A Pilot Study of 68Ga-FAPI-RGD PET/CT Imaging in the Lung Cancer Patients [NCT05543954]Early Phase 160 participants (Anticipated)Interventional2022-09-03Recruiting
The Novel 18F-labeled MAO-B PET/CT Imaging on Parkinsonism Patients of Chinese Population: a Prospective Study [NCT06010290]80 participants (Anticipated)Observational2022-11-30Recruiting
A Phase II Trial of Surgery and Fractionated Re-Irradiation for Recurrent Ependymoma [NCT02125786]Phase 270 participants (Anticipated)Interventional2014-05-07Active, not recruiting
Radioguided Detection of Lymph Node Metastasis in Non-Small Cell Lung Cancer [NCT00732563]100 participants (Actual)Interventional2008-07-16Completed
Prospective Study Evaluating the Combination of Positron Emission Tomography (PET) With 18F-FDG and 18 F-Fluorocholine for Optimization of Staging and Treatment Modification in Patients With Hepatocellular Carcinoma [NCT04391348]230 participants (Actual)Interventional2020-07-17Completed
PET/MR, PET/CT and Whole Body MR in Newly Diagnosed Acute Myeloid Leukemia (AML) [NCT02390635]Phase 155 participants (Anticipated)Interventional2016-05-02Recruiting
Quantitative Dynamic PET and MRI and Breast Cancer Therapy [NCT01931709]35 participants (Actual)Interventional2011-11-30Terminated(stopped due to Terminated due to end of funding)
A Multicenter Trial to Measure Early Patterns of Change in [18F]-Fluorodeoxyglucose Uptake by PET/CT in Relapsed Ovarian Cancer Patients [NCT00959582]Phase 142 participants (Actual)Interventional2009-09-30Completed
MRI- and PET-Predictive-Assay of Treatment Outcome in Cancer of the Cervix [NCT01992861]51 participants (Actual)Observational2014-02-14Terminated
Efficacy of [18F]-2-fluoro-2-deoxy-D-glucose Positron Emission Tomography (FDG-PET) in Evaluation of Cytological Indeterminate Thyroid Nodules Prior to Surgery: a Multicentre Cost-effectiveness Study [NCT02208544]132 participants (Actual)Interventional2015-07-16Completed
Evaluating Sunitinib Therapy in Renal Cell Carcinoma Using F-18 FDG PET/CT and DCE MRI [NCT00537056]17 participants (Actual)Interventional2007-10-31Completed
Pilot Study Evaluating a Combined and Integrated Technological Approach of F-18-FDG-Directed Perioperative PET/CT Imaging and Intraoperative Handheld Gamma Prove Detection of Known and Occult Disease in Patients Undergoing Surgery for Solid Malignancies [NCT00816335]Early Phase 165 participants (Actual)Interventional2008-10-31Completed
Evaluation of the Sensitivity and Reproducibility of 18F-fluorodeoxyglucose Positron Emission Tomography Coupled With Magnetic Resonance Imaging for the Assessment of Respiratory Muscle Activity and Relationships With Multiparametric Respiratory Muscle Ul [NCT05234099]16 participants (Anticipated)Interventional2022-05-05Recruiting
A Phase II, Single-center STudy on the vAlue of Non-invasive Dual-Pet(18F-FES PET and 68Ga-HER2-Affibody PET)InformatiOn IN Subtype of Metastatic Breast Cancer(MBC) [NCT04758416]50 participants (Anticipated)Observational2020-12-31Recruiting
Phase II Trial: uPAR PET/CT and FDG PET/MRI for Preoperative Staging of Bladder Cancer [NCT02805608]Phase 240 participants (Anticipated)Interventional2016-09-30Active, not recruiting
FDG-PET Based Chemotherapy Selection for Metastatic Non-Small Cell Lung Cancer [NCT00564733]Phase 255 participants (Actual)Interventional2007-10-31Completed
EXPLORER Total Body PET/CT Imaging for Myofascial Pain [NCT05876858]Early Phase 153 participants (Anticipated)Interventional2023-06-13Recruiting
A Single Case Study of Hypermetabolism [NCT04805268]1 participants (Actual)Interventional2020-12-14Completed
A Pilot Bioimaging Trial of Cancer Cachexia [NCT04127981]40 participants (Anticipated)Interventional2019-03-28Recruiting
Diagnostic Assessment of 18F-fluciclovine and 18F-FDG - PET/MRI of Primary Central Nervous System Lymphoma [NCT03188354]10 participants (Anticipated)Interventional2017-11-01Recruiting
An Open-label, Non-randomized Study to Monitor for Adverse Drug Reactions Among Patients Administered Fedoruk-manufactured [F-18]-FDG Injection [NCT02811185]Phase 41,012 participants (Actual)Interventional2016-06-30Completed
Prospective Evaluation of PET-CT Scan in Patients With Non-operable or Non-resectable NSCLC Treated by Radical 3-Dimensional Conformal Radiation Therapy [NCT00958321]Phase 240 participants (Anticipated)Interventional2007-03-31Terminated(stopped due to Low levels of recruitment)
Research on the Lymphoma Staging and Therapeutic Evaluation of 18F-FDG PET/CT Comparing With Whole Body MRI IVIM Functional Imaging [NCT02733887]66 participants (Anticipated)Interventional2016-02-29Recruiting
A Multicenter Phase 2 Study Comparing 99m Tc EC-DG SPECT/CT With 18F FDG PET/CT in the Evaluation of Patients With Non-small Cell Lung Cancer (NSCLC) [NCT00865319]Phase 222 participants (Actual)Interventional2009-06-30Completed
Evaluation of Brain Functional Changes With 18F-FDG PET and Cognitive Processes After Brain Radiotherapy for Cavernous Sinus Meningiomas and Non-secreting ACTH Adenomas [NCT06180226]20 participants (Actual)Observational2008-04-21Completed
A Randomized Phase 3 Interim Response Adapted Trial Comparing Standard Therapy With Immuno-oncology Therapy for Children and Adults With Newly Diagnosed Stage I and II Classic Hodgkin Lymphoma [NCT05675410]Phase 31,875 participants (Anticipated)Interventional2023-05-11Recruiting
A Phase III Randomized Study of Maintenance Nivolumab Versus Observation in Patients With Locally Advanced, Intermediate Risk HPV Positive OPSCC [NCT03811015]Phase 3636 participants (Anticipated)Interventional2019-08-16Recruiting
Contribution of PET/MRI in Locally Advanced Cervical Cancer [NCT06083103]50 participants (Anticipated)Observational2023-10-02Not yet recruiting
PET Biodistribution Study of 68Ga-FAPI-46 in Patients With Different Malignancies: An Exploratory Biodistribution Study With Histopathology Validation [NCT04459273]Phase 130 participants (Anticipated)Interventional2020-08-27Recruiting
PET Biodistribution Study of 68Ga-PSMA-11 and 68Ga-FAPI-46 in Patients With Non-Prostate Cancers: An Exploratory Biodistribution Study With Histopathology Validation [NCT04147494]Early Phase 130 participants (Anticipated)Interventional2019-11-05Recruiting
"Phase II Study of Sunitinib (SU011248) in Patients With Small Cell Lung Cancer Who Are Either Chemo-naïve (Extensive Disease) or Have a Sensitive Relapse" [NCT00953459]Phase 29 participants (Actual)Interventional2009-02-28Terminated(stopped due to poorly recruiting)
Creating Metabolic Vulnerabilities in Patients With EGFR Activated Recurrent Glioblastoma by Inhibiting EGFR With Osimertinib [NCT03732352]Phase 212 participants (Actual)Interventional2018-11-28Active, not recruiting
Assessing Hypoxia by 18F-EF5 PET Scanning and Glycolysis by 18FFDG PET Scanning in Subjects With Non-Small Cell Lung Cancer [NCT01017133]Phase 156 participants (Anticipated)Interventional2009-05-31Completed
The Diagnostic Value of 18F-2-fluoro-2-deoxy-D-glucose Fluorodeoxyglucose-Positron-Emission-Tomography/Magnetic-Resonance Imaging (PET/MRI) for Cervical Lymph Node Metastasis in Head and Neck Squamous Cell Carcinoma [NCT04117139]142 participants (Anticipated)Interventional2019-10-01Recruiting
Treatment of Opioid-refractory Pain (WHO Level III) by Pituitary Radiosurgery: A Multicenter, Prospective, Randomized Study [NCT02637479]40 participants (Anticipated)Interventional2015-12-31Recruiting
Non-invasive Diagnosis and Management of Subclinical Rejection in Kidney Transplant Patients Using 18F-fluorodeoxy Glucose Positron Emission Tomography (18FDG-PET/CT) [NCT04702022]50 participants (Anticipated)Interventional2021-01-04Recruiting
Diagnostic and Prognostic Significance of Combined PET/MRI in Inflammatory Cardiomyopathies and Sarcoidosis [NCT03356756]60 participants (Anticipated)Observational2016-06-27Recruiting
A Pilot Study of 18F Fluorothymidine (FLT) PET/CT in Lymphoma [NCT00775268]Phase 1/Phase 231 participants (Actual)Interventional2008-09-29Terminated
Phase 2 Study With the Multi-Targeted Tyrosine-Kinase Inhibitor Pazopanib (GW786034) for Patients With Relapsed or Refractory Urothelial Cancer [NCT01031875]Phase 241 participants (Anticipated)Interventional2009-12-31Completed
CLDN18.2 Targeting Nanobody Probe for PET Imaging in Solid Tumors [NCT05436093]15 participants (Anticipated)Interventional2022-06-23Recruiting
Phase II Multi-Institutional Study to Evaluate the Efficacy of Gemcitabine and Fractionated Stereotactic Radiotherapy for Unresectable Pancreatic Adenocarcinoma [NCT01146054]Phase 259 participants (Actual)Interventional2009-10-31Completed
Phase II Single-Arm Trial Comparing the Use of FLT PET to Standard Computed Tomography to Assess the Treatment Response of Neoadjuvant Docetaxel and Cisplatin in Stage IB-IIIA Resectable Non-small Cell Lung Cancer [NCT00963807]Phase 226 participants (Actual)Interventional2009-09-30Completed
Utility of Preoperative FDG-PET/CT Scanning Prior to Primary Chemoradiation Therapy to Detect Retroperitoneal Lymph Node Metastasis in Patients With Locoregionally Advanced Carcinoma of the Cervix (IB2, IIA ≥ 4 CM, IIB-IVA) or Endometrium (Grade 3 Endomet [NCT00416455]Phase 1/Phase 2384 participants (Actual)Interventional2007-09-30Completed
Imaging Biomarkers for Immune Checkpoint Inhibitor Treatment in Patients With Non-small Cell Lung Cancer: Prospective Observational Study [NCT05260606]100 participants (Anticipated)Observational [Patient Registry]2022-05-09Recruiting
Single-tracer Multiparametric PET Imaging [NCT06014515]Early Phase 160 participants (Anticipated)Interventional2024-01-31Recruiting
A Randomized Phase II Trial of Ofatumumab and Bendamustine vs. Ofatumumab, Bortezomib (NSC # 681239) and Bendamustine in Patients With Untreated Follicular Lymphoma [NCT01286272]Phase 2135 participants (Actual)Interventional2011-04-08Active, not recruiting
Breast Imaging Screening Studies in Women at High Genetic Risk of Breast Cancer: Annual Follow-up Study [NCT00006421]200 participants (Actual)Observational2000-10-25Completed
A Pilot Study of 64Cu-DOTA-Trastuzumab Positron Emission Tomography in Treatment of Advanced HER2 Positive Breast Cancer With the Antibody Drug Conjugate Ado-trastuzumab Emtansine [NCT02226276]10 participants (Actual)Interventional2015-01-07Active, not recruiting
Determination of Molecular Status, as Well as the Efficacy and Safety of Fluorodeoxyglucose (18F-FDG) in PET-CT Imaging in Juvenile Patients With Histiocytosis [NCT04943211]Phase 3150 participants (Anticipated)Interventional2021-04-01Recruiting
Pilot Study of Ex-Vivo Molecular Polyp Imaging Using 18-F Fluorodeoxyglucose (FGD) Positron Emission Tomography (PET) in the Determination of Protein and Gene Expression Signatures of Premalignant Polyps [NCT00550628]8 participants (Actual)Observational2007-09-30Completed
Evaluation of Metabolic Changes in FDG PET/CT Imaging After mRNA-based COVID-19 Vaccination [NCT05270967]129 participants (Actual)Observational2021-07-29Completed
A Multi-Center Phase 1b Pharmacokinetic and Radiation Dosimetry Study Evaluating 99mTc-EC-DG SPECT/CT in Patients With Non-small Cell Lung Cancer (NSCLC) [NCT00864110]Phase 14 participants (Actual)Interventional2010-04-30Completed
PET-imaging of Unruptured Intracranial Aneurysm Inflammation [NCT04715503]20 participants (Anticipated)Interventional2021-01-14Recruiting
A Phase 2 Study of Triapine® (NSC #663249) and Cisplatin in Combination With Pelvic Radiation for Treatment of Stage IB2-IVa Cervical Cancer or Stage II-IV Vaginal Cancer [NCT00941070]Phase 226 participants (Actual)Interventional2009-07-31Completed
PD-L2 Targeting Nanobody Radiotracer for PET Imaging of Solid Tumor [NCT05803746]20 participants (Anticipated)Interventional2022-07-15Recruiting
A Study to See if a New Type of Imaging Can Help Our Understanding of the Course of Non-small Cell Lung Cancer in Patients Undergoing Treatment With Radiotherapy or Chemoradiotherapy [NCT00765986]30 participants (Anticipated)Observational2008-10-31Recruiting
Contribution of Positron Emission Tomography in Biological Targeting by Conformational Radiotherapy and Intensity-modulated Radiotherapy of Ear, Nose and Throat Tumors [NCT00809016]40 participants (Anticipated)Interventional2007-05-31Completed
A Phase II Study of Single Agent Intravenous (IV) VEGF Trap in Patients With Poor Prognostic Recurrent and/or Metastatic Thyroid Cancer After RAI Therapy [NCT00729157]Phase 241 participants (Actual)Interventional2008-08-31Completed
A Pilot Study of Dual Time Point FDG PET MR Imaging Optimization for the Evaluation of Brain Metastasis [NCT05054998]Phase 420 participants (Anticipated)Interventional2018-08-03Recruiting
Role of Early 18F-FDG-PET/CT Scan in Predicting Mediastinal Downstaging With Neoadjuvant Chemotherapy in Resectable Stage III A NSCLC [NCT02607423]Phase 20 participants (Actual)Interventional2015-11-19Withdrawn(stopped due to The study failed to meet its accrual targets.)
Early Changes in 18F-fluorodeoxyglucose Positron Emissions Tomography (18F-FDG-PET/CT) Scan as Predictors of Clinical Outcome in NSCLC Treated With EGFR Tyrosin Kinase Inhibitors (TKI) [NCT02043002]67 participants (Actual)Interventional2013-04-30Completed
Study of Positron Emission Tomography With 18-fluorodeoxyglucose in Detecting Cancer in Patients With Idiopathic Venous Thromboembolism [NCT00964275]400 participants (Actual)Interventional2009-03-31Completed
Epileptogenic Focus Localization for Children With Epilepsy Using 18F-FDG PET Molecular Imaging [NCT04725162]234 participants (Actual)Observational2014-07-01Completed
18F-FDG Metabolism Imaging Monitoring Non-small Cell Lung Cancer Curative Effect of Chemotherapy Multicenter Clinical Study [NCT02938546]Phase 3200 participants (Anticipated)Interventional2016-11-30Not yet recruiting
Phase I Trial of Adaptive 18F-FDG-PET Biological Intensity-modulated Radiotherapy (BG-IMRT) With Patients With Head and Neck Tumor [NCT00406289]Phase 124 participants (Anticipated)Interventional2006-11-30Completed
A Multicenter Trial of FDG-PET/CT Staging of Head and Neck Cancer and Its Impact on the N0 Neck Surgical Treatment in Head and Neck Cancer Patients [NCT00983697]292 participants (Anticipated)Interventional2010-04-01Active, not recruiting
Early Positron Emission Tomography as a Predictor of Response in Neoadjuvant Chemotherapy for Non-Small Cell Lung Cancer [NCT00227539]Phase 225 participants (Actual)Interventional2005-07-31Completed
Molecular Imaging of Cerebral Amyloid Plaques Using PET With Fluoro Tracker for Early Diagnosis of Alzheimer's Disease [NCT01325259]Phase 254 participants (Actual)Interventional2009-04-30Completed
Use of Integrated PET/CT as a First Line Staging and Re-staging Technique in Oncologic Patient. [NCT06168877]30 participants (Actual)Observational2009-10-21Completed
Biodistribution of [11C]Acetoacetate/[18F]Fluorodeoxyglucose in Subjects With Varying Risk Factors for Alzheimer's Disease and Subjects on a Diet Intervention [NCT03130036]60 participants (Anticipated)Interventional2015-06-09Enrolling by invitation
An Evaluation of Preoperative Chemotherapy With Irinotecan and Cisplatin for Advanced, But Resectable Gastric Cancer: A Coordinated Multidisciplinary, Multicenter Study Linking Functional Imaging, Genomic Expression Profiles and Histopathology [NCT00062374]Phase 255 participants (Actual)Interventional2003-06-30Completed
Multicenter Prospective Pilot Study Investigating Pathophysiology, Diagnostic and Therapeutic Strategies of Hepatosplenic Candidiasis [NCT01916057]100 participants (Actual)Interventional2013-11-19Completed
Autologous Blood or Marrow Transplantation for Aggressive Non-Hodgkin's Lymphoma Based on Early [18F] FDG-PET Scanning [NCT00238368]Phase 259 participants (Actual)Interventional2004-02-29Completed
FDG PET/MR Imaging of Peripheral Pain Generators in Persistent Post-Surgical Pain (PPSP) [NCT06171659]128 participants (Anticipated)Observational2023-12-31Recruiting
The Beneficial Value of 18F FDG PET/CT in the Follow-up of Stage III Non-small Cell Lung Cancer Patients: the NVALT31-PET Study [NCT06082492]690 participants (Anticipated)Interventional2023-12-31Not yet recruiting
RELATIONSHIP BETWEEN THORACIC AORTIC STRUCTURE ASSESSED BY PET/CT SCAN AND ARTERIAL STIFFNESS IN ELDERLY PATIENTS: FICTEP STUDY [NCT01963221]30 participants (Actual)Interventional2010-01-31Completed
A Randomized Phase III Trial of Induction/Consolidation Atezolizumab (NSC #783608) + SBRT Versus SBRT Alone in High Risk, Early Stage NSCLC [NCT04214262]Phase 3480 participants (Anticipated)Interventional2020-08-13Recruiting
Phase I Dose Escalation of Neoadjuvant Proton Beam Radiotherapy With Concurrent Chemotherapy in Locally Advanced Esophageal Cancer [NCT02213497]Phase 130 participants (Anticipated)Interventional2014-04-30Active, not recruiting
Evaluation of 18F-2-fluoro-2-deoxy-D-glucose Produced by a New Manufacturer, for Safety, Through the Identification of Adverse Events, and Efficacy, Through the Evaluation of Its Ability, When Utilized in Performance of a Positron Emission Tomography Comp [NCT04615156]Phase 310,000 participants (Anticipated)Interventional2020-11-01Not yet recruiting
Positron Emission Tomography Using 11C Topotecan in Predicting Response to Treatment in Patients With Brain Metastases Due to Ovarian, Small Cell Lung, or Other Cancer [NCT00253461]Early Phase 17 participants (Actual)Interventional2004-12-31Terminated(stopped due to Drugs unavailable:unable to make radioactive topotecan)
Initial Human Validation of Simultaneous Dual-Tracer Cardiac PET Imaging [NCT02003456]Early Phase 130 participants (Actual)Interventional2013-12-31Completed
Clinical Applications of Fibroblast Activation Protein Inhibitor-Based Dimeric Radiotracer 68Ga-DOTA-F2 PET/CT Imaging for Malignant Tumors [NCT05637034]30 participants (Anticipated)Interventional2022-09-15Recruiting
A Phase II Trial to Evaluate Functional Imaging in Prediction of Response to Abemaciclib for Advanced Hormone Receptor-Positive, HER2-Negative Breast Cancer [NCT06179303]Phase 260 participants (Anticipated)Interventional2024-06-01Not yet recruiting
A Phase II Trial Evaluating 18F-Fluciclovine PET/CT in Multiple Myeloma [NCT06103838]Phase 255 participants (Anticipated)Interventional2024-01-03Not yet recruiting
Phase II Trial of Response-Adapted Chemotherapy Based on Positron Emission Tomography for Non-Bulky Stage I and II Hodgkin Lymphoma [NCT01132807]Phase 2164 participants (Actual)Interventional2010-05-31Completed
Dissection of Aorta: Descending Part, Imaging [NCT01648881]89 participants (Actual)Observational2011-05-31Completed
68Ga-FAP-CHX PET/CT : Dosimetry and Preliminary Clinical Translational Studies [NCT05506566]Phase 1/Phase 250 participants (Anticipated)Interventional2022-05-01Recruiting
Normative Values for Cognitive Testing and Alzheimer's Imaging Biomarkers in Young Adults (30-49yo) [NCT01609335]Phase 141 participants (Actual)Interventional2012-07-31Completed
Early Assessment of Response to Dual Checkpoint Inhibitor Therapy in Patients With Advanced Melanoma Using 18F-FLT PET/CT and PET/MR [NCT02891616]Phase 14 participants (Actual)Interventional2016-10-10Terminated(stopped due to Low accrual rate)
A Phase 2 Study of Positron Emission Tomography Imaging With [18F]-Fluoromisonidazole (FMISO) and [18F]-Fluorodeoxyglucose (FDG) for Assessment of Tumor Hypoxia in Soft Tissue Sarcoma [NCT01169350]Phase 28 participants (Actual)Interventional2010-02-28Terminated(stopped due to funding source ended earlier than anticipated)
Effects of Chemotherapy on Brain Structure and Function [NCT00755313]81 participants (Actual)Observational2007-05-31Completed
Vorinostat to Augment Response to Lutetium-PSMA-617 in the Treatment of Patients With PSMA-Low Metastatic Castration-Resistant Prostate Cancer [NCT06145633]Phase 215 participants (Anticipated)Interventional2024-04-01Not yet recruiting
Creation of a Database of PET Digital Brain Exams, Adapted to a Population Aged 50 Years and Over, to Help in the Interpretation of Fluoro Desoxy Glucose (FDG) Labelled With Fluor 18 (18F-FDG) PET/CT (Computer Tomography) Exam [NCT04163276]80 participants (Actual)Observational2008-01-02Completed
A Prospective Study of the Diagnostic Accuracy of the Augmented Whole-body Scanning Via Magnifying PET (AWSM-PET) Technique Versus the Standard-of-care (SOC) FDG PET/CT for Malignant Lesion Detection [NCT05513027]35 participants (Anticipated)Interventional2024-01-31Not yet recruiting
Longitudinal Assessment of Amyloid Positron Emission Tomography (PET), Fludeoxyglucose F18 (FDG) PET, Tau PET, Magnetic Resonance Imaging (MRI), and Blood Spot Ribonucleic Acid (RNA) in Down Syndrome Individuals With and Without Alzheimer's Dementia and N [NCT02759887]19 participants (Actual)Interventional2016-11-30Completed
FDG and FDOPA PET Demonstration of Functional Brain Abnormalities [NCT04315584]Early Phase 15 participants (Anticipated)Interventional2020-03-15Recruiting
Evaluation of Somatostatin Receptor Imaging Using PET/MRI as a Novel Approach to Detecting Pathology in Pulmonary TB [NCT02845570]Phase 18 participants (Anticipated)Interventional2016-07-31Recruiting
Reproducibility of 18F-FDG Uptake Measurements in Malignant Solid Tumors on PET/CT and PET/MR [NCT02717572]Phase 119 participants (Actual)Interventional2016-03-01Completed
Prospective Longitudinal Observation Trial of Clinical and Molecular Features of Pancreatic Neuroendocrine Tumours [NCT03741517]40 participants (Anticipated)Observational [Patient Registry]2019-01-30Recruiting
Longitudinal Measurement of Synaptic Density to Monitor Progression of Huntington's Disease. [NCT04701580]33 participants (Actual)Interventional2020-01-14Completed
Combined 68Ga-DOTATATE and 18F-FDG PET/CT Imaging in Patients With Well-differentiated, G2-G3, Gastroenteropancreatic (GEP)-Neuroendocrine Tumors (NETs) - A Pilot Study [NCT04804371]40 participants (Anticipated)Interventional2021-03-04Active, not recruiting
NORM: Nodular Lymphocyte-Predominant Hodgkin Lymphoma Patients Treated in a Randomized Phase II Trial With Either Rituximab or Mosunetuzumab [NCT05886036]Phase 270 participants (Anticipated)Interventional2024-07-27Recruiting
A Prospective Study on Predicting the Efficacy of Neoadjuvant Chemotherapy in Locally Advanced Gastric Cancer. [NCT05140746]40 participants (Anticipated)Interventional2020-09-10Recruiting
Dual Time Point FDG PET Imaging Optimization for the Evaluation of Glioblastoma [NCT02885272]Early Phase 121 participants (Actual)Interventional2016-10-28Completed
A Pilot Study of 18FDG-PET Imaging to Detect Changes in Airways Inflammation in Cystic Fibrosis Patients After Treatment for a Pulmonary Exacerbation [NCT00684346]Phase 320 participants (Actual)Interventional2008-04-30Completed
Comparison of 18F-2-fluoro-2-deoxy-D-glucose (18F-FDG) PET/CT and Ultrasound in Staging of Patients With Malignant Melanoma: An Analysis in a Single Patient Population [NCT04253574]258 participants (Actual)Observational2014-09-01Completed
Creation of a Probabilistic Atlas of Normal Cerebral Uptake of 18F-FDG in PET/MRI. [NCT05355857]39 participants (Actual)Interventional2022-08-10Completed
Comparison of I-124 PET/CT, F-18 FDG PET/CT and I-123 Whole Body Scintigraphy for Recurrent Thyroid Cancer Detection [NCT00373711]0 participants (Actual)Observational2007-05-31Withdrawn(stopped due to Abandoned)
Interim FDG-PET/CT for PreDIcting REsponse of HER2+ Breast Cancer to Neoadjuvant Therapy: DIRECT Trial [NCT05710328]Phase 2235 participants (Anticipated)Interventional2023-05-10Recruiting
Use of [18F]FDG PET/MRI in the Diagnosis of Pain Generators and/or Sites of Inflammation and to Monitor Treatment Effects in Patients With Chronic Pain [NCT03195270]Phase 188 participants (Actual)Interventional2014-11-24Completed
Simultaneous Fluorodeoxyglucose and Magnetic Resonance Imaging (18F-FDG PET/MR) Study of Metabolic and Structural Changes in Visual Snow Syndrome Compared to Healthy Controls [NCT05569733]22 participants (Actual)Observational2017-01-02Completed
A Phase I Study Evaluating the Efficacy and Toxicity of Stereotactic Body Radiation for Metastatic or Recurrent Platinum-Resistant Ovarian Cancer [NCT01494012]Phase 11 participants (Actual)Interventional2012-04-30Terminated(stopped due to low accrual)
Monitoring Targeted Lung Cancer Treatments With FDG-PET/CT [NCT00450567]36 participants (Actual)Observational2004-12-31Completed
The H10 EORTC/GELA/IIL Randomized Intergroup Trial on Early FDG-PET Scan Guided Treatment Adaptation Versus Standard Combined Modality Treatment in Patients With Supradiaphragmatic Stage I/II Hodgkin's Lymphoma [NCT00433433]Phase 31,952 participants (Actual)Interventional2006-10-31Active, not recruiting
Phase I/II Study on Induction Chemotherapy Followed by Chemoradiation With or Without Lapatinib, a Dual EGFR/ErbB2 Kinase Inhibitor, in Patients With Locally Advanced Larynx and Hypopharynx Squamous Cell Carcinoma [NCT00498953]Phase 1/Phase 27 participants (Actual)Interventional2007-05-31Completed
Very Early Response Monitoring in Patients With Glioblastoma Undergoing Therapy Using FDG PET/CT [NCT02902757]50 participants (Anticipated)Interventional2015-08-25Recruiting
d68Ga-DOTATATE PET/CT Assessment of Cardiac Sarcoidosis [NCT03549598]Phase 415 participants (Actual)Interventional2018-07-20Completed
Evaluating Fluorine-18 Fluorodeoxyglucose Positron Emission Tomography /Computed Tomography With Liver SUVmax-based Criteria for Prognosis of Patients With Diffuse Large B-cell Lymphoma [NCT02931201]100 participants (Anticipated)Interventional2016-10-31Recruiting
18F-FDG PET/CT-based Prognostic Model for Predicting Outcome in Patients With Diffuse Large B-cell Lymphoma [NCT02928861]100 participants (Anticipated)Interventional2016-10-31Recruiting
Improved Visualization of Glioblastoma Using Delayed 18F-FDG PET/CT. [NCT02919332]0 participants (Actual)Observational2016-06-08Withdrawn(stopped due to No participants were enrolled)
Nectin-4 Specific LMW PET Probe Imaging in Urothelial Carcinoma [NCT05321316]20 participants (Anticipated)Interventional2022-05-31Recruiting
Clinical Evaluation of PET-MRI Versus PET-CT in Pediatric Oncology Patients [NCT02287636]13 participants (Actual)Interventional2013-04-30Completed
A Pilot Study of Novel Imaging Modalities in Monoclonal Gammopathy of Undetermined Significance (MGUS), Smoldering Multiple Myeloma (SMM), and Multiple Myeloma (MM) [NCT01237054]Phase 231 participants (Actual)Interventional2010-10-17Completed
Serial [F-18] Fluoroestradiol (FES) PET Imaging to Evaluate Endocrine-Targeted Therapy [NCT02149173]29 participants (Actual)Interventional2010-09-15Terminated(stopped due to Terminated due to low accrual)
Evaluation of 18F-FDG PET/CT in Diagnosis and Response Assessment of Patients With IgG4-Related Disease [NCT01665196]Early Phase 1100 participants (Anticipated)Interventional2012-09-30Recruiting
Glucidic Metabolism, Ossification and Arterial Calcification During PseudoXanthoma Elasticum (PXE) [NCT03070860]23 participants (Actual)Interventional2016-11-30Completed
Distribution of Eosinophils in Asthma After Reslizumab (DEAR). A 7-Week, Placebo-Controlled, Double-Blinded, Parallel-Group, Imaging Study Using Positron Emission Tomography/Computer Tomography (PET/CT) to Characterize the Effect of Intravenous Reslizumab [NCT02937168]Phase 45 participants (Actual)Interventional2017-05-08Terminated(stopped due to The study was terminated early due to challenges in recruitment. The decision to terminate the study was not related to any safety issues or concerns.)
A Pilot Study to Compare 18F-Fluorodeoxyglucose Positron Emission Tomography (PET) Scanning in Addition to CT Scanning With CT Scanning Alone in the Pre-Operative Evaluation of Patients With Stage III and IV Melanoma [NCT00004152]Phase 20 participants Interventional1999-02-28Completed
18F-FDG PET/CT in Diagnostic Patients of Disorder of Consciousness [NCT02999490]20 participants (Actual)Interventional2016-03-31Completed
Optimized Arterial Spin Labeling MRI for Cognitive Decline [NCT01727622]102 participants (Actual)Observational2012-08-31Completed
Investigation of the Use of Positron Emission Tomography With 18F-FDG PET/CT for the Diagnosis of Synovitis in the Temporomandibular Joint [NCT01471418]Phase 20 participants (Actual)Interventional2011-12-31Withdrawn(stopped due to 29-Apr-14 UPENN IRB granted approval to close study due to lack of funding)
A Phase II Trial of Sequential SGN-35 Therapy With Adriamycin, Vinblastine, and Dacarbazine (S-AVD) for Older Patients With Untreated Hodgkin Lymphoma [NCT01476410]Phase 248 participants (Actual)Interventional2011-11-30Active, not recruiting
Positron Emitter I-124-Iododeoxyuridine to Follow DNA Metabolism on Scans and in Tumor Samples in Advanced Breast Cancer: Comparison to 18-F-2-Fluoro-2-Deoxy-(D)-Glucose, as a Tracer for Glycolysis [NCT00109785]Phase 18 participants (Actual)Interventional1997-03-31Completed
Diagnostic Performance of 18F-FDG-PET and Diffusion-weighted MRI in the Assessment of Stage IB to IIB2 Cervical Squamous-cell Carcinoma Response to Concomitant Radiochemotherapy and Brachytherapy [NCT01663753]146 participants (Actual)Interventional2012-03-31Completed
68Ga-FAPI-04 PET Imaging in Early Response Evaluation of Rectal Cancer Patients Treated With Immunotherapy: A Single-center Clinical Study [NCT05999227]20 participants (Anticipated)Interventional2023-06-20Recruiting
Serial [F-18] Fluoroestradiol (FES) PET Imaging to Evaluate Endocrine-targeted Therapy [NCT04692103]Phase 22 participants (Actual)Interventional2021-07-10Active, not recruiting
Phase II Trial of Doxorubicin, Vinblastine, and Gemcitabine (AVG) Chemotherapy for Non-Bulky Stage I and II Hodgkin's Lymphoma [NCT00086801]Phase 2104 participants (Actual)Interventional2004-05-31Completed
Phase II Study of BAY 43-9006 in Patients With Metastatic Thyroid Carcinoma [NCT00095693]Phase 225 participants (Actual)Interventional2004-10-31Terminated
First International Inter-Group Study for Classical Hodgkin's Lymphoma in Children and Adolescents [NCT00433459]Phase 32,134 participants (Actual)Interventional2007-01-31Completed
Prognostic Significance of Early Positron Emission Tomography (PET) With Fluorine-18 Fluorodeoxyglucose ([18F] FDG) in Intermediate and High Grade Non-Hodgkin's Lymphoma [NCT00110006]0 participants (Actual)Interventional2004-12-31Withdrawn(stopped due to No accrual)
A Pilot Study on the Efficacy of Advanced 18F-FDG PET-MRI in Spine Stereotactic Radiosurgery [NCT05174026]10 participants (Actual)Interventional2018-11-30Active, not recruiting
FDG PET to Assess Therapeutic Response in Patients With Bone-Dominant Metastatic Breast Cancer, FEATURE [NCT04316117]Phase 2138 participants (Actual)Interventional2020-09-15Active, not recruiting
A Randomized Phase II/III Trial of De-Intensified Radiation Therapy for Patients With Early-Stage, P16-Positive, Non-Smoking Associated Oropharyngeal Cancer [NCT03952585]Phase 2/Phase 3590 participants (Anticipated)Interventional2019-10-09Suspended(stopped due to End of Initial Phase of Multi-phase protocol)
Serial Imaging of the Novel Radiotracer [^18F] FLuorthanatrace ([^18F] FTT) by PET/CT [NCT03604315]Phase 1120 participants (Anticipated)Interventional2018-12-18Recruiting
International Multicenter Trial on the Prognostic Value of Arterial 18F-FDG PET Imaging in Patients With History of Myocardial Infarction [NCT05138718]2,041 participants (Anticipated)Observational [Patient Registry]2021-12-01Recruiting
A Pilot Study to Assess the Feasibility of Detection and Quantification of Differences in Hodgkin Lymphoma and Diffuse Large B-cell Lymphoma Using FDG-PET/CT Imaging [NCT01004718]10 participants (Actual)Interventional2009-05-31Completed
Phase II Study of Pralatrexate and Docetaxel in Patients With Advanced Esophageal and Gastroesophageal Carcinoma Who Have Failed Prior Platinum-based Therapy. [NCT01129206]Phase 26 participants (Actual)Interventional2010-07-31Completed
A Pilot Comparison of 68Ga-P16-093 and 18F-FDG PET/CT Imaging in the Same Group of Clear Cell Renal Cell Carcinoma Patients [NCT05432947]42 participants (Actual)Interventional2022-04-14Completed
A Phase II Trial of PET-Directed Therapy for Limited Stage Diffuse Large B-Cell Lymphoma (DLBCL) [NCT01359592]Phase 2159 participants (Actual)Interventional2011-09-30Active, not recruiting
Optimizing Acquisition Parameters and Interpretive Methods of FDG-PET/CT With Rb-82 Myocardial Perfusion Imaging for Evaluation of Cardiac Sarcoidosis [NCT03048097]Early Phase 115 participants (Actual)Interventional2017-02-01Completed
Direct Imaging of Ischemia With 18F-FDG PET Imaging Combined With Coronary Anatomy From CT Coronary Angiography [NCT01520025]Phase 418 participants (Actual)Interventional2011-12-31Terminated(stopped due to Continued recruitment of study participants was not feasible)
Cognitive and Emotional Disorders in Amyotrophic Lateral Sclerosis : Neuropsychological, Imaging and Neuropathological Study [NCT01530438]90 participants (Anticipated)Interventional2009-04-30Recruiting
Phase I Trial of The Combination of Vismodegib and Sirolimus [NCT01537107]Phase 131 participants (Actual)Interventional2012-03-05Completed
A Prospective Study of the Predictive and Prognostic Value of Multimodalitic Imaging in the N-stage of Lung Cancer [NCT05840094]100 participants (Anticipated)Interventional2023-05-01Not yet recruiting
Prospective Evaluation of 18F-Fluorodeoxyglucose Positron Emission Tomography (FDG-PET) in the Multimodality Management of Locally Advanced Primary Rectal Cancer [NCT00004891]149 participants (Actual)Interventional1999-09-30Completed
A Pilot Study To Assess The Utility Of 18F-Fluorodeoxyglucose Positron Emission Tomography (PET) In The Pre-Operative Evaluation Of Patients With Primary And Recurrent Breast Carcinoma [NCT00039286]Phase 1118 participants (Actual)Interventional2001-10-31Completed
Phase II Study of the Role of Anti-CEA Antibody Immunoscintigraphy & Positron Emission Tomography in the Localization of Recurrent Colorectal Carcinoma in Patients With Rising Serum CEA Levels in the Absence of Imageable Disease by Conventional Modalities [NCT00001568]Phase 2200 participants Interventional1997-02-28Completed
Study on the Prediction of Groin Lymphonodal Status Through 18FDG-PET/CT Combined With Sentinel Lymph Node Biopsy in Bulky a/o Multifocal a/o Pretreated Vulvar Cancer, N0 at Conventional Imaging (GRO-SNaPET Study) [NCT02969278]50 participants (Anticipated)Interventional2013-07-31Recruiting
Detection of Hepatocellular Carcinoma by Positron Emission Tomography With C-Acetate-11 and F-fluorodeoxyglucose-18 [NCT00081094]31 participants (Actual)Interventional2003-09-30Completed
Positron Emission Tomography Pre- and Post-treatment Assessment For Locally Advanced Non-Small Cell Lung Carcinoma [NCT00083083]Phase 2250 participants (Anticipated)Interventional2005-03-31Active, not recruiting
[18F]FDG-PET/CT as a Predictive Marker of Tumor Response and Patient Outcome: Prospective Validation in Non-Small Cell Lung Cancer [NCT00424138]96 participants (Actual)Interventional2007-03-30Terminated(stopped due to Recruitment obstacles; data to be combined with other resources for analysis)
Phase 1-2 18F-FPPRGD2 PET/CT or PET/MRI Imaging of αvβ3 Integrins Expression as a Biomarker of Angiogenesis [NCT01806675]Phase 1/Phase 225 participants (Actual)Interventional2013-03-04Completed
Energy Expenditure and Brown Adipose Tissue in Amyotrophic Lateral Sclerosis [NCT03150290]10 participants (Actual)Interventional2017-10-26Completed
64Cu-DOTATATE PET-CT-skanning to Diagnose Macrophage Infiltration in the Heart Valves of Patients With Infective Endocarditis. [NCT05432427]65 participants (Anticipated)Interventional2022-04-28Recruiting
The Use of Positron Emission Tomography (PET) and Magnetic Resonance Imaging (MRI) to Assess the Effects of Anti-neoplastic Therapy on Tumor Associated Vasculature [NCT00019565]Phase 153 participants (Actual)Interventional1998-10-31Completed
A Study Evaluating the Imaging Characteristics of Florbetapir 18F (18F-AV-45) in Patients With Frontotemporal Dementia Compared to Patients With Alzheimer's Disease and Normal Controls. [NCT01890343]Phase 234 participants (Actual)Interventional2009-09-30Completed
A Phase I Clinical, Pharmacokinetic and Pharmacodynamic Study of Flavopiridol in Patients With Refractory Solid Tumors and Hematologic Malignancies [NCT00070239]Phase 1100 participants (Actual)Interventional2003-08-31Terminated
Comparison of Positron Nuclide Labeled DOTA-FAPI PET and FDG PET Study in Colocrectal Cancer [NCT04750772]60 participants (Anticipated)Interventional2019-10-16Recruiting
A Phase III Randomized Trial of FDG-PET in the Management of Advanced Cervical Cancer With Enlarged Pelvic Lymph Node on MRI Image [NCT00146458]Phase 3200 participants Interventional2002-01-31Active, not recruiting
A Study Of 18 FDG PET In The Prediction Of Relapse In Patients With A Clinical Stage I Non-Seminomatous Germ Cell Tumor [NCT00045045]0 participants Interventional2002-05-31Completed
[NCT00200668]0 participants (Actual)Interventional2005-03-31Terminated
A Phase 2 Study of Positron Emission Tomography Imaging With [18F]-Fluoromisonidazole (FMISO) and [18F]-Fluorodeoxyglucose (FDG) for Assessment of Tumor Hypoxia in Cervical Cancer [NCT00559377]Phase 216 participants (Actual)Interventional2007-11-30Completed
Assessment of Diagnostic Accuracy of 18FDG-PET-CT in Patients With Suspicion of Pacing or Defibrillation Lead Infection: a Prospective Multi-center Study [NCT02251262]235 participants (Actual)Interventional2015-06-22Completed
The Utility of FDG-PET and PET/CT in the Evaluation of Patients With Suspected Cholecystitis [NCT00590395]19 participants (Actual)Interventional2007-07-31Completed
Pilot Project for Creation of the DLBCL Response Prediction Model: Combining Early Interim Functional Imaging, Detection of a Tumor-Specific Clonotype and Metabolic Profiling of Blood of in Patients With Relapsed/Refractory Diffuse Large B-Cell Lymphoma t [NCT02405078]Early Phase 135 participants (Actual)Interventional2015-10-13Completed
Assessment of the Heterogeneity of Estrogen Receptor Expression in Patients With Estrogen Receptor Positive Breast Cancer Using F-18 Fluoroestradiol and High Resolution Positron Emission Mammography [NCT03266562]0 participants (Actual)Interventional2018-09-01Withdrawn(stopped due to unable to recruit patients due to competing studies)
A Phase II Trial of AZD0530 in Previously Treated Metastatic Pancreas Cancer [NCT00735917]Phase 219 participants (Actual)Interventional2008-10-31Completed
Positron Nuclide Labeled NOTA-FAPI PET Study in Lymphoma [NCT04367948]200 participants (Anticipated)Interventional2020-05-01Not yet recruiting
Characterization of Radiolabeled Tracer Uptake Pattern in Noninfected Transcatheter Aortic Valves. The COUNT Study. A Prospective, Observational Study. [NCT03683355]30 participants (Anticipated)Observational2018-11-09Active, not recruiting
CT Abnormalities Evocative of Lung Infection Are Associated With Lower 18F-FDG Uptake in Confirmed COVID-19 Patients [NCT04512118]22 participants (Actual)Observational2020-03-15Completed
Evaluation of PET-MRI in Initial Staging of High Grade Rectal Cancer Patients and in the Follow up of Colorectal Cancer Patients. [NCT01807117]15 participants (Actual)Interventional2013-04-30Completed
18F-FDG PET/CT in the Diagnosis of Tuberculous Pericarditis [NCT05458089]11 participants (Actual)Observational2015-01-01Completed
Evaluation of 18F-DCFPyL PSMA- Versus 18F-NaF-PET Imaging for Detection of Metastatic Prostate Cancer [NCT03173924]Phase 2180 participants (Anticipated)Interventional2017-06-06Enrolling by invitation
Randomized Phase II Trial of Individualized Adaptive Radiotherapy Using During-Treatment FDG-PET/CT and Modern Technology in Locally Advanced Non-Small Cell Lung Cancer (NSCLC) [NCT01507428]Phase 2138 participants (Actual)Interventional2012-02-22Active, not recruiting
PiB PET Scanning in Speech and Language Based Dementias [NCT01623284]Phase 1168 participants (Actual)Interventional2010-03-31Completed
A Phase II Study of the Combination of Aflibercept (VEGF-Trap) Plus Modified FOLFOX 6 in Patients With Previously Untreated Metastatic Colorectal Cancer [NCT01652196]Phase 256 participants (Actual)Interventional2012-11-14Active, not recruiting
LCCC 1209: Pilot Study of [18F] Fluorodeoxyglucose Positron Emission Tomography-Magnetic Resonance Imaging (FDG-PET-MRI) for Staging of Muscle-Invasive Bladder Cancer [NCT01655745]22 participants (Actual)Interventional2012-07-24Completed
Non-Invasive Cerenkov Luminescence Imaging of Lymphoma, Leukemia and Metastatic Lymph Nodes [NCT01664936]27 participants (Actual)Observational2012-08-08Completed
LCCC 1213: Defining Molecular and Functional Imaging Correlates of Renal Cell Carcinoma Biological Features [NCT01665703]17 participants (Actual)Interventional2012-08-31Completed
PET Quantitative Assessments of Solid Tumor Response to Immune Checkpoint Blockade Therapy [NCT01666353]Early Phase 120 participants (Actual)Interventional2012-04-16Completed
Dual-Time Point (DTP) FDG PET CT for the Post-Treatment Assessment of Head and Neck Tumors Following Definitive Chemoradiation Therapy [NCT03575949]50 participants (Anticipated)Interventional2018-06-15Recruiting
SiCARIO (Split Course Adaptive Radioimmunotherapy) for the Treatment of Oligometastatic Non-Small Cell Lung Cancer (NSCLC) Using Biologically-Adaptive Radiotherapy - A Phase I/II Study [NCT05501665]Phase 1/Phase 225 participants (Anticipated)Interventional2023-05-09Recruiting
Reliability Of The Human Brain Connectome [NCT02193425]Early Phase 1112 participants (Actual)Interventional2015-06-08Completed
FDG PET/CT: Reducing False Positive Mediastinal Uptake by Premedicating With Methylprednisolone [NCT01789892]0 participants (Actual)Interventional2011-06-30Withdrawn(stopped due to no patient accrual)
The Differential Diagnosis of Parkinson's Disease and Parkinsonism by Positron-emission Tomography With Vesicular Monoamine Transporter Ligand (18F-DTBZ) [NCT01824056]Phase 2120 participants (Actual)Interventional2010-08-31Completed
A Pilot Study of the Utility of 18F-FLT-PET and Diffusion-Weighted MRI for Surgical Planning, Radiotherapy Target Delineation, and Treatment Response Evaluation in Ewing Sarcoma Patients [NCT01825902]Early Phase 11 participants (Actual)Interventional2013-03-31Completed
A Single-blind Study to Evaluate the Efficacy and Safety of 18F-Fluorodeoxygalactose (18F-FDGal) Compared to 18F-Fluorodeoxyglucose (18F-FDG) to Detect Hepatocellular Carcinoma Via PET/CT in Patients With Cirrhosis or Chronic Liver Disease [NCT02899325]0 participants (Actual)Observational2019-10-31Withdrawn(stopped due to PIs will not pursue trial due to staff and time constraints)
A Pilot Study of Vorinostat to Restore Sensitivity to Aromatase Inhibitor Therapy Part B [NCT01720602]15 participants (Actual)Interventional2012-11-30Completed
A Phase 2, Open-label, Single-arm, Efficacy and Imaging Study of Oral Enzalutamide in Chemo-Naïve Patients With Progressive Prostate Cancer Who Have Failed Androgen Deprivation Therapy (Castration-resistant Prostate Cancer Patients) [NCT02814968]Phase 266 participants (Actual)Interventional2015-02-28Completed
Personalized Radiation Therapy Through Functional Lung Avoidance and Response-Adaptive Dose Escalation: Utilizing Multimodal Molecular Imaging to Improve the Therapeutic Ratio (FLARE RT) [NCT02773238]Phase 256 participants (Actual)Interventional2016-05-20Completed
Investigation of AlzHeimer's Predictors in Subjective Memory Complainers - Extension Study [NCT05806697]240 participants (Anticipated)Interventional2023-04-17Not yet recruiting
Positron Emission Tomography for the Diagnosis of Immune Checkpoint Inhibitor-Related Myocarditis [NCT05062395]13 participants (Actual)Observational2021-03-30Completed
Intra-operative Lymph Node Evaluation Using a Hand Held PET Gamma Probe in Endometrial Cancer Surgery - A Pilot Study [NCT01467219]12 participants (Actual)Interventional2012-01-31Completed
A Phase 2A Study to Evaluate Safety, Tolerability and Pharmacological Effects of PU AD in Subjects With Mild Alzheimer's Disease (AD) Dementia [NCT04311515]Phase 24 participants (Actual)Interventional2020-06-30Terminated(stopped due to Samus Therapeutics company closure)
Assessment of the Minimal Residual Disease in Diffuse Large B-Cell Lymphomas (DLBCL) From Cell-free Circulating DNA by Next Generation Sequencing (NGS) [NCT02339805]30 participants (Actual)Interventional2014-11-01Completed
A Pilot Study of Sirolimus (Rapamycin, Rapamune[Registered Trademark]) in Subjects With Cowden Syndrome or Other Syndromes Characterized by Germline Mutations in PTEN [NCT00971789]Phase 218 participants (Actual)Interventional2008-07-31Completed
FDG-PET/CT as a Biomarker for Treatment Response in Advanced Melanoma [NCT02236546]3 participants (Actual)Interventional2012-05-31Terminated(stopped due to loss of funding)
[F18]EF5 PET/CT Imaging in Patients With Locally Advanced or Recurrent/Metastatic Carcinoma of the Cervix [NCT00978874]15 participants (Actual)Interventional2008-05-31Terminated(stopped due to The PI is no longer with our institution)
A Phase 2 Study of [18F] Fluoroestradiol (FES) as a Marker of Hormone Sensitivity of Metastatic Breast Cancer [NCT00602043]Phase 220 participants (Actual)Interventional2008-09-30Completed
Multi-tracer PET Assessment of Response in Various Malignancies in Investigational and Recently Approved Therapeutic Agents [NCT01243333]26 participants (Actual)Interventional2011-02-02Terminated
Novel Imaging Modalities For Plexiform Neurofibromas [NCT00060008]18 participants (Actual)Interventional2002-04-30Terminated(stopped due to Study was closed early due to poor accrual.)
The Utility of Positron Emission Tomography (PET) in Staging of Patients With Potentially Operable Non-Small Cell Lung Carcinoma [NCT00004138]303 participants (Actual)Interventional1999-09-30Completed
Longitudinal Early-onset Alzheimer's Disease Study Protocol [NCT03507257]700 participants (Anticipated)Observational2018-04-30Recruiting
Multimodal Functional Imaging Combined With Metabolomics in Predicting the Efficacy of Neoadjuvant Chemoradiotherapy for Locally Advanced Esophageal Squamous Cell Carcinoma [NCT04759235]118 participants (Anticipated)Observational2020-01-01Recruiting
11C-Methionine and 2-18F-Fluoro-2-Deoxy-D-Glucose PET Imaging in Patients With Progressive Prostate Cancer [NCT00002981]173 participants (Actual)Interventional1997-01-31Completed
Evolution of Lung 18FDG Uptake in Patients With Idiopathic Pulmonary Fibrosis and Receiving Pirfenidone [NCT03692481]50 participants (Anticipated)Interventional2020-02-04Recruiting
A 2 Phase Comparison of Pre-operative CT AND PET Images in the Intraoperative Detection of Disease to a Hand-held Probe, and to an Intraoperative CT Scan in Patients Undergoing Surgery for Metastatic Colorectal Cancer. [NCT01821105]Phase 221 participants (Actual)Interventional2004-03-31Completed
PET Imaging of Lung Cancer and Indeterminate Pulmonary Nodules With 18F-FSPG [NCT02448225]Phase 246 participants (Actual)Interventional2015-06-16Completed
Does Ultra Short-term Steroid Therapy Increase the Accuracy of FDG-PET/CT in Evaluation of Pulmonary Nodules? [NCT00906503]Phase 19 participants (Actual)Interventional2009-04-30Completed
Value of PET/ CT in the 68Ga-NODAGA-RGD for the Evaluation of the Tumoral Neoangiogenesis [NCT02666547]Phase 1120 participants (Anticipated)Interventional2014-03-31Recruiting
T Cell Effector and Regulatory Mechanisms in Asthma [NCT01612936]Phase 1168 participants (Actual)Interventional2012-09-30Completed
Adoptive Transfer of NY-ESO-1 TCR Engineered Peripheral Blood Mononuclear Cells (PBMC) After a Nonmyeloablative Conditioning Regimen, With Administration of NY-ESO-1157-165 Pulsed Dendritic Cells and Interleukin-2, in Patients With Advanced Malignancies [NCT01697527]Phase 26 participants (Actual)Interventional2012-11-02Active, not recruiting
PET/CT Evaluation of Subjects Treated on Surgery Branch Adoptive Cell Therapy Protocols [NCT00316901]Phase 270 participants (Anticipated)Interventional2006-04-30Completed
Evaluation of a Low-Carbohydrate Diet to Highlight Easily Infective Endocarditis by 18F-FDG PET [NCT03465098]26 participants (Actual)Interventional2018-03-19Completed
Noninvasive Assessment of Abdominal Aortic Aneurysm (AAA) Wall Structural Integrity and Inflammation as Predictors of Expansion and/or Rupture [NCT03231397]Phase 42 participants (Actual)Interventional2017-08-01Terminated(stopped due to We were unable to recruit more subjects who met the inclusion/exclusion criteria and we have closed the study.)
Whole-Body 18F-Fluorodeoxyglucose Positron Emission Tomography to Measure the Response to Induction Chemotherapy of Potentially Resectable Lung and Esophageal Carcinomas [NCT00002930]Phase 2/Phase 375 participants (Anticipated)Interventional1996-12-31Completed
Biological Interconnection Between Stress-associated Neurobiological Activity and Atherosclerotic Plaque Instability: A Prospective Cohort Study With OCT-FLIM Dual-modal Intravascular Imaging and Serial 18F-FDG-PET/CT Assessment [NCT04853511]200 participants (Anticipated)Observational [Patient Registry]2022-02-14Recruiting
The Utility of Positron Emission Tomography (PET) in Staging of Patients With Potentially Operable Carcinoma of the Thoracic Esophagus [NCT00004867]235 participants (Actual)Interventional1999-11-30Completed
Natural History of Metabolic Abnormalities in Children With Epilepsy [NCT00001325]80 participants Observational1992-04-30Completed
Comparative Study of 18F-FAPI and 18F-FDG PET/CT for Gastrointestinal Cancer [NCT05788874]50 participants (Anticipated)Observational2023-05-31Not yet recruiting
Stress and Atherosclerotic Plaque Macrophages: A Systems Biology Approach - PET/MRI of the Brain-hematopoiesis-atherosclerosis Axis in PTSD Patients [NCT03279393]Early Phase 1190 participants (Actual)Interventional2017-11-28Completed
PET Imaging of Breast Cancer Using Oncogene Expression [NCT02810873]19 participants (Actual)Interventional2008-09-30Terminated(stopped due to Study terminated by PI)
PET/CT-Guided Liver Tumor Ablation: Intraprocedural Assessment of Results Using Ammonia Perfusion PET [NCT02018107]33 participants (Actual)Interventional2014-01-31Completed
Copper Cu 64-ATSM and PET/CT Scan in Predicting Disease Progression in Patients With Newly-Diagnosed Stage IB, Stage II, Stage III, or Stage IVA Cervical Cancer Who Are Undergoing Chemoradiotherapy Per NCCN Guidelines [NCT00794339]Phase 273 participants (Actual)Interventional2009-07-29Terminated(stopped due to transfer of funding)
A Pilot Study of 18F-Flourodeoxyglucose Positron Emission Tomography in the Diagnosis of Primary and Recurrent Cervical Cancer [NCT00003429]0 participants Interventional1998-05-31Completed
Phase I Study of Dose Escalation Using Image-guided Radiotherapy to Deliver a Stereotactic Radiosurgical Boost After Neoadjuvant Chemoradiotherapy in Patients With Locally Advanced Esophageal Cancer [NCT00368329]Phase 14 participants (Actual)Interventional2006-06-30Terminated(stopped due to low accrual)
A Head-to-head Comparative Study of 18F-PSMA-1007 PET/CT and 18F-FDG PET/CT Imaging in Multiple Myeloma [NCT05448404]30 participants (Anticipated)Interventional2022-03-08Recruiting
Evaluation Via PET Scan of Metabolic Anomolies Associated With the 6 Month Clinical Evolution of Patients Suffering From Motor Conversion Disorder [NCT02329626]20 participants (Actual)Observational2016-01-29Completed
PET Biodistribution Study of 68Ga-FAPI-46 in Patients With Sarcoma: An Exploratory Biodistribution Study With Histopathology Validation [NCT04457258]Early Phase 130 participants (Anticipated)Interventional2020-09-08Recruiting
18F-FDG PET/CT-based Prognostic Model for Predicting Outcome in Patients With Natural Killer/T-cell Lymphoma [NCT03051555]60 participants (Anticipated)Interventional2017-03-01Not yet recruiting
Evaluation of the Use of Intra-operative Molecular Imaging With BetaScope and in Vitro Measurement With LightPath Specimen Analyser Devices in Gastrointestinal Tumour Surgery [NCT02446379]0 participants (Actual)ObservationalWithdrawn(stopped due to Technology licensed to third party. Sponsor did not proceed with study.)
Prediction and Unraveling of Delayed Cerebral Ischemia in Patients With Subarachnoid Hemorrhage Using Early Dynamic 18F-FDG PET/CT Assessment of Cerebral Glucose Uptake (PREDISP) [NCT04356599]35 participants (Anticipated)Interventional2020-07-22Recruiting
[NCT02394743]360 participants (Actual)Observational2011-03-31Completed
Study of Metabolic Connectivity in Drug-resistant Temporal Epilepsy [NCT05455047]90 participants (Actual)Observational2022-02-01Completed
Radiomics and Metabolomics in the Follow-up of CAR T-cells for Refractory or Relapsed Non-Hodgkin's Lymphoma: Pilot Study [NCT05422521]20 participants (Anticipated)Interventional2022-08-29Recruiting
Individualized Precise Radiotherapy With the Guidance of Radiosensitivity: A Study on the Clinical Management Model of Locally Advanced Cervical Cancer [NCT03163979]Phase 2/Phase 3300 participants (Anticipated)Interventional2015-07-01Recruiting
Evaluating the Potential Usefulness of 68Ga-FAP-2286 PET/CT in Patients With Various Types of Cancer and Compared With 18F-FDG PET/CT [NCT05392205]67 participants (Actual)Interventional2022-03-01Completed
The Potential Role of Ga-68-PSMA in Staging, Restaging and Monitoring Response in Primary Liver Cancer: Comparison With F-18-FDG [NCT03138239]16 participants (Anticipated)Interventional2017-07-02Not yet recruiting
Usefulness of 18F-FDG PET/CT in the Initial Staging and Surveillance of Endometrial Cancer Patients [NCT05056259]42 participants (Anticipated)Observational2022-01-01Not yet recruiting
Head-to-head Comparison of Diagnosis Value of Pulmonary Fibrosis on 68Ga-FAPI-04 and 18F-FDG PET-CT [NCT05121779]Phase 180 participants (Anticipated)Interventional2021-12-01Not yet recruiting
68Ga-FAPI-RGD PET/CT for Dual Integrin αvβ3 and FAP-targeted Imaging in Patients With Various Types of Cancer and Compared With 18F-FDG [NCT05543317]27 participants (Actual)Interventional2022-07-01Completed
Immunostart: Prephase Tafasitamab, Retifanlimab, and Rituximab (TRR), Followed by TRR-CHOP, for Previously Untreated Diffuse Large B-Cell Lymphoma [NCT05455697]Phase 1/Phase 235 participants (Anticipated)Interventional2023-01-26Recruiting
Clinical Application of 18F-PEG3-FPN PET Imaging in Diagnosis and Staging of Malignant Melanoma [NCT04747561]50 participants (Anticipated)Interventional2021-01-12Recruiting
A Pilot Prospective Study of the Utility of Dynamic Contrast-Enhanced Magnetic Resonance Imaging (DCE-MRI), Diffusion Weighted MRI (DWI)and Positron Emission Tomography (PET) Imaging With 18F-Fluorodeoxyglucose (18FDG) in Brachytherapy for Cervix Cancer [NCT01899404]25 participants (Actual)Interventional2012-10-03Completed
Detection of Functioning Pituitary Microadenoma With Inconclusive MRI Findings: PET/MRI Versus PET/CT [NCT03404414]Phase 1100 participants (Anticipated)Interventional2013-02-28Recruiting
The Use of Radiofrequency Ablation to Treat Hepatic Neoplasms [NCT00019604]Phase 244 participants (Actual)Interventional1998-08-31Terminated(stopped due to Principal investigator left the institution.)
Early Assessment of Response to Targeted Breast Cancer Therapy [NCT00362973]42 participants (Actual)Observational2006-05-31Completed
Imaging of Intracerebral Inflammation in the Progressive Phase of Multiple Sclerosis [NCT02305264]61 participants (Actual)Interventional2012-03-19Completed
Lu-177-DOTATATE (Lutathera) in Therapy of Inoperable Pheochromocytoma/ Paraganglioma [NCT03206060]Phase 290 participants (Anticipated)Interventional2017-10-10Recruiting
A Phase II Trial of Limited Surgery and Proton Therapy for Craniopharyngioma and Observation for Craniopharyngioma After Radical Resection [NCT01419067]Phase 2112 participants (Actual)Interventional2011-08-22Active, not recruiting
Diagnostic Accuracy of MRI, Diffusion-weighted MRI, FDG-PET/CT and Fluoro-ethyl-choline PET/CT in the Detection of Lymph Node Metastases in Surgically Staged Endometrial and Cervical Carcinoma [NCT01836484]162 participants (Actual)Observational2012-06-30Completed
A Pivotal Phase 3 Clinical Trial to Assess the Diagnostic Performance and Safety of [68Ga]Ga-PentixaFor ([68Ga]Ga-PTF), a Positron Emission Tomography (PET) Imaging Agent, Versus [18F]FDG PET/CT Imaging, for Staging of Patients With Confirmed Marginal Zon [NCT06125028]Phase 3148 participants (Anticipated)Interventional2023-12-15Not yet recruiting
A Phase II Study of 17-Allylamino-17-Demethoxygeldanamycin in Patients With Von Hippel Lindau Disease and Renal Tumors [NCT00088374]Phase 29 participants (Actual)Interventional2004-07-31Completed
Particle-based Partial Tumor Irradiation Targeting Hypoxic Segment and Sparing the Peritumoral Immune Microenvironment for Unresectable Bulky Tumors [NCT04875871]22 participants (Anticipated)Interventional2021-11-11Recruiting
18F-FDG PET/CT-based Prognostic Model for Predicting Outcome in Patients With Peripheral T-cell Lymphoma [NCT03051581]80 participants (Anticipated)Interventional2017-03-01Not yet recruiting
Evaluating the Potential Usefulness of 18F-AlF-FAPI PET/CT in Patients With Gastrointestinal Tumors and Compared With 18F-FDG PET/CT [NCT05430841]100 participants (Anticipated)Interventional2022-06-01Recruiting
Feasibility and Outcome of Cyberknife® Precision Hypofractionated Radiosurgery for the Curative Management of Non-Small Cell Lung Cancer [NCT00852644]9 participants (Actual)Interventional2009-01-31Terminated(stopped due to poor accrual)
Polymyalgia Rheumatica and Giant Cell Arteritis - Three Challenges - Consequences of the Vasculitis Process, Osteoporosis and Malignancy: A Prospective Cohort Study Protocol [NCT02985424]80 participants (Anticipated)Observational2017-05-31Not yet recruiting
A Prospective Study to Evaluate 68Ga-FAPI-04 and 18F-FDG PET/CT in Patients With Epithelial Ovarian Cancer: Compared With Histological Findings [NCT04504110]Phase 230 participants (Anticipated)Interventional2020-08-05Recruiting
The Prognostic Value of 18F-PFPN PET Imaging in Patients With Malignant Melanoma [NCT05645484]100 participants (Anticipated)Observational2022-09-02Recruiting
TocilizuMab discontinuAtion in GIant Cell Arteritis [NCT06037460]Phase 3120 participants (Anticipated)Interventional2024-01-31Not yet recruiting
Elucidating Mechanisms of Pain in Adolescent and Adult Fibrous Dysplasia Patients [NCT04125862]40 participants (Anticipated)Interventional2021-01-05Enrolling by invitation
Is Mediastinal Blood Pool SUV Ratio Valid in Identification of Malignancy in Comparison to Liver SUV Ratio? [NCT05258045]55 participants (Anticipated)Observational2022-06-01Not yet recruiting
[NCT02481726]Phase 1/Phase 231 participants (Actual)Interventional2014-03-31Completed
Prospective Longitudinal Biomarker Study in Pancreatic Neuroendocrine Tumours [NCT03130205]30 participants (Anticipated)Observational2017-05-01Recruiting
Evaluation of Regional Myocardial Perfusion, Glucose Utilization and Oxidative Metabolism in Patients With Pulmonary Hypertension Using Combined [11C]Acetate and [18F]Fluorodeoxyglucose (FDG) PET/CT and Cardiovascular MRI [NCT01917136]Phase 221 participants (Actual)Interventional2013-08-31Completed
Diagnostic Value of 18F-fluorodeoxyglucose Positron Emission Tomography/Computed Tomography in Prosthetic Valve Endocarditis [NCT01916005]174 participants (Actual)Interventional2014-02-05Completed
Evaluation of the Safety and Sensitivity of 68Ga-DOTATOC PET/CT for Imaging NET Patients [NCT03583528]800 participants (Anticipated)Observational2018-07-11Recruiting
PET Imaging of Hepatocellular Carcinoma With 18F-FSPG [NCT02379377]Phase 180 participants (Anticipated)Interventional2022-02-15Recruiting
Highlighting the Benefits of Therapeutic Gardens in Alzheimer's Disease by 18F-FDG Cerebral PET /CT [NCT04514328]0 participants (Actual)Interventional2022-08-02Withdrawn(stopped due to the study never opened for pandemic reasons)
Contribution of PET Scans for the Preoperative Assessment of Symptomatic Endometriosis Lesions: TEP-ENDORUN [NCT04831619]Phase 310 participants (Anticipated)Interventional2022-05-31Not yet recruiting
Phase II Trial of Hypo-fractionated Highly Conformal Radiotherapy for Locally Advanced Pancreatic Carcinomas [NCT05191940]30 participants (Anticipated)Interventional2022-05-16Recruiting
Role of Positron Emission Tomography/Computed Tomography in Detecting Bone Metastases in Cancer Patients. [NCT04080271]66 participants (Actual)Observational2019-11-01Completed
Preoperative Image-guided Identification of Response to Neoadjuvant Chemoradiotherapy in Esophageal Cancer [NCT03474341]200 participants (Anticipated)Observational2018-04-09Recruiting
A Phase II Clinical Trial to Evaluate 18F-Fluoroestradiol Positron Emission Tomography / Computerized Tomography (PET/CT) Guided Fulvestrant Therapy for Patients With Recurrent or Metastatic Breast Cancer [NCT00816582]17 participants (Actual)Interventional2010-11-30Terminated(stopped due to Slow accrual)
Phase II Study Evaluating the Role of Pazopanib in Angiosarcoma [NCT01462630]Phase 229 participants (Actual)Interventional2011-11-03Completed
Phase II Study of PET-Directed Frontline Therapy With Pembrolizumab and AVD for Patients With Classical Hodgkin Lymphoma [NCT03226249]Phase 230 participants (Actual)Interventional2017-11-09Active, not recruiting
Integrating Biomarkers From Serum/Plasma and Molecular Images to Predict Occult Distant Metastases in Nasopharyngeal Carcinoma Patients With M0 Disease [NCT04417985]112 participants (Actual)Interventional2011-08-01Completed
Comparison of the Performance of 18F-FDG PET/CT With That of Labeled Leukocyte Scintigraphy in the Follow-up of Malignant Otitis Externa. [NCT05994768]18 participants (Actual)Observational2020-12-18Completed
An Evaluation of PET/CT Imaging as a Predictor of Disease Free Survival Following Neo-Adjuvant Chemotherapy for Soft Tissue Sarcoma [NCT00346125]70 participants (Actual)Interventional2006-04-10Completed
Illiteracy and Vulnerability to Alzheimer's Disease: Evaluation of Amyloid Pathology by PET Imaging [NCT02494531]45 participants (Actual)Interventional2015-12-12Completed
Ultra-long Field-Of-View Positron Emission Tomography for Characterization of Indeterminate Lung Nodules: a Pilot Study Exploring Opportunities for Clinical Research [NCT05463913]Phase 420 participants (Anticipated)Interventional2022-07-13Recruiting
A Prospective Study to Evaluate the Inflammation and Fibrosis of Intestinal Stricture in Patients With Crohn's Disease by 18F-FDG and 68Ga-FAPI PET/CT [NCT04502303]Phase 230 participants (Anticipated)Interventional2020-09-30Not yet recruiting
Phase II Study of Decitabine in Patients With Metastatic Papillary Thyroid Cancer or Follicular Thyroid Cancer Unresponsive to Radioiodine [NCT00085293]Phase 212 participants (Actual)Interventional2004-05-31Completed
Early Response Evaluation With 18F-FDG PET/CT and Immunological Profiling of Circulating Immune Cells and Tumor-draining Lymph Nodes in Non-small Cell Lung Cancer Patients Treated With Immunotherapy. [NCT04082988]9 participants (Actual)Interventional2018-01-23Terminated(stopped due to The study has been closed due to slow enrollment.)
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Trial Outcomes

TrialOutcome
NCT00019604 (2) [back to overview]Response
NCT00019604 (2) [back to overview]Number of Participants With Adverse Events
NCT00043979 (14) [back to overview]Early Post Transplantation Relapse
NCT00043979 (14) [back to overview]Median Progression Free Survival
NCT00043979 (14) [back to overview]Median Time to Reach a Platelet Count of 50,000/mm(3)
NCT00043979 (14) [back to overview]Two Year Survival Rate for Patients Undergoing Allo-Hematopoietic Stem Cell Transplant
NCT00043979 (14) [back to overview]Median Time to Reach Absolute Neutrophil Count of 500/mm(3)
NCT00043979 (14) [back to overview]Number of Participants Who Experienced Graft Versus Tumor Effect (GVT)
NCT00043979 (14) [back to overview]Number of Participants With Engraftment
NCT00043979 (14) [back to overview]Cluster of Differentiation 4 (CD4) Reconstitution
NCT00043979 (14) [back to overview]Toxicity
NCT00043979 (14) [back to overview]Best Response Post-Hematopoietic Stem Cell Transplant EOCH (Etoposide, Vincristine, Cyclophosphamide, and Doxorubicin)
NCT00043979 (14) [back to overview]Median Survival From Date of Progression
NCT00043979 (14) [back to overview]Number of Participants to Complete Conversion to >95% Donor Chimerism
NCT00043979 (14) [back to overview]Number of Participants With Acute and Chronic GVHD
NCT00043979 (14) [back to overview]Post-Hematopoietic Stem Cell Transplant (HSCT) Radiotherapy
NCT00060008 (1) [back to overview]Tumor Progression as Measured by Tumor Area and Volume at 1 Year.
NCT00062374 (2) [back to overview]Histological Response Determined by FDG Uptake Correlates
NCT00062374 (2) [back to overview]Disease Free Survival (DFS)
NCT00085293 (2) [back to overview]Frequency of Adverse Events According to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0
NCT00085293 (2) [back to overview]Restoration of Radioiodine Uptake in Metastatic Lesions as Demonstrated by Diagnostic Whole-body Scanning After Decitabine Administration
NCT00088374 (5) [back to overview]The Number of Participants With Adverse Events
NCT00088374 (5) [back to overview]Number of Patients in Whom Renal Tumors Could be Identified by Positron Emission Tomography (PET)Based on Fludeoxyglucose 18F (18FDG) Uptake
NCT00088374 (5) [back to overview]Number of Participants With Flow Dynamics Measured by DCE MRI Within the Renal and Non-renal Tumor
NCT00088374 (5) [back to overview]Number of Participants With a Renal Tumor Response
NCT00088374 (5) [back to overview]Number of Participants With a Non-renal Tumor Response
NCT00227539 (3) [back to overview]Positron Emission Tomography as a Predictor of Response Measured by the Decrease in Standard Uptake Variable (SUV) After 1 Course of Therapy
NCT00227539 (3) [back to overview]Safety of Neoadjuvant Chemotherapy
NCT00227539 (3) [back to overview]Efficacy of Neoadjuvant Chemotherapy as Measured by Radiologic Response Rate
NCT00375830 (9) [back to overview]Cohort 1 - 18F-NaF PET/CT vs 18F-FDG PET/CT
NCT00375830 (9) [back to overview]Cohort 1 - NaF PET/CT vs 99mTc-MDP Bone Scintigraphy
NCT00375830 (9) [back to overview]Cohort 2 - 18F-NaF/18F-FDG PET/CT vs Whole-body MRI for Detection of Extraskeletal Lesions
NCT00375830 (9) [back to overview]Cohort 2 - 18F-NaF/18F-FDG vs 99mTc-MDP Bone Scintigraphy for Detection of Skeletal Lesions
NCT00375830 (9) [back to overview]Cohort 2 - 18F-NaF/18F-FDG vs Whole-body MRI for Detection of Skeletal Lesions
NCT00375830 (9) [back to overview]Cohort 2 - Overall Sensitivity and Accuracy for 18F-NaF/18F-FDG vs Whole-body MRI
NCT00375830 (9) [back to overview]Cohort 2 - Overall Sensitivity and Accuracy for 18F-NaF/18F-FDG vs Whole-body MRI/99mTc-MDP Bone Scintigraphy
NCT00375830 (9) [back to overview]Cohort 3 - Total Skeletal Lesions Identified, Tc-99m MDP WBBS vs 18F-NaF / 18F-FDG PET/MRI
NCT00375830 (9) [back to overview]Cohort 3 - Skeletal Lesions Identified by 99mTc MDP WBBS vs 18F-NaF / 18F-FDG PET/MRI
NCT00381797 (26) [back to overview]Progression-free Survival Hazard Ratio by VEGF-A Expression
NCT00381797 (26) [back to overview]Progression-free Survival Hazard Ratio by Carbonic Anhydrase 9 (CA9) Expression
NCT00381797 (26) [back to overview]Progression-free Survival Hazard Ratio by Hypoxia Inducible Factor-2alpha Expression
NCT00381797 (26) [back to overview]Correlation of the Change in Vascular Endothelial Growth Factor Receptor-2 (VEGF-R2) Expression in Peripheral Blood Mononuclear Cells (PBMC) From Baseline With the Change in Perfusion From Magnetic Resonance Imaging
NCT00381797 (26) [back to overview]Progression-free Survival Hazard Ratio by VEGF-R2 Expression
NCT00381797 (26) [back to overview]Sustained Disease Stabilization Rate Associated With Bevacizumab and Irinotecan in Patients With Recurrent or Progressive Low-grade Glioma (Stratum E)
NCT00381797 (26) [back to overview]Systemic Clearance
NCT00381797 (26) [back to overview]Terminal Half-life
NCT00381797 (26) [back to overview]Volume of Distribution
NCT00381797 (26) [back to overview]Association of Log-transformed Tumor Diffusion Ratio With Progression-free Survival (PFS) Using Hazard Ratio Estimates
NCT00381797 (26) [back to overview]Association of Log-transformed Tumor Enhancing Volume With Progression-free Survival (PFS) Using Hazard Ratio Estimates
NCT00381797 (26) [back to overview]Association of Log-transformed Tumor Volume Based on FLAIR With Progression-free Survival (PFS) Using Hazard Ratio Estimates
NCT00381797 (26) [back to overview]Association of Log-transformed Volume of Cystic Necrosis With Progression-free Survival (PFS) Using Hazard Ratio Estimates
NCT00381797 (26) [back to overview]Change in Diffusion Ratio Between the Baseline and Day 15 Brain Image
NCT00381797 (26) [back to overview]Change in Perfusion Ratio Between the Baseline and Day 15 Brain Imaging
NCT00381797 (26) [back to overview]Change in Vascular Endothelial Growth Factor Receptor-2 (VEGF-R2) Expression in Peripheral Blood Mononuclear Cells (PBMC) From Baseline to Day-15
NCT00381797 (26) [back to overview]Cumulative Incidence of Sustained Objective Responses
NCT00381797 (26) [back to overview]Descriptive Statistics for the Change of Perfusion in Magnetic Resonance Imaging Concurrently Measured With the Change in Vascular Endothelial Growth Factor Receptor-2 (VEGF-R2) Expression in Peripheral Blood Mononuclear Cells (PBMC)
NCT00381797 (26) [back to overview]Descriptive Statistics for the Changes in Vascular Endothelial Growth Factor Receptor-2 (VEGF-R2) Expression in Peripheral Blood Mononuclear Cells (PBMC) Concurrently Measured With the Changes in Perfusion From Magnetic Resonance Imaging
NCT00381797 (26) [back to overview]Number of Patients With High Carbonic Anhydrase 9 Expression at Baseline
NCT00381797 (26) [back to overview]Number of Patients With High Hypoxia Inducible Factor-2alpha Expression at Baseline
NCT00381797 (26) [back to overview]Number of Patients With High VEGF-A Expression at Baseline
NCT00381797 (26) [back to overview]Number of Patients With High VEGF-R2 Expression at Baseline
NCT00381797 (26) [back to overview]Number of Study Participants With Grade 3 or 4 Treatment-related Toxicity
NCT00381797 (26) [back to overview]Objective Response Rate Sustained for ≥ 8 Weeks
NCT00381797 (26) [back to overview]Progression-free Survival
NCT00416455 (15) [back to overview]The Diagnostic Specificity of PET/CT for Detection of Lymph Node Metastasis in Pelvis
NCT00416455 (15) [back to overview]Specificity for Detection of Lymph Node Metastasis in Abdomen by CT Alone
NCT00416455 (15) [back to overview]The Diagnostic Sensitivity of PET/CT for Detection of Lymph Node Metastasis in Pelvis
NCT00416455 (15) [back to overview]Sensitivity for Detection of Lymph Node Metastasis in Abdomen by CT Alone
NCT00416455 (15) [back to overview]The Diagnostic Specificity of PET/CT for Detection of Lymph Node Metastasis in Combination of Abdomen and Pelvis
NCT00416455 (15) [back to overview]Specificity Between for Detection of Lymph Node Metastasis in Pelvis by CT Alone
NCT00416455 (15) [back to overview]Sensitivity for Detection of Lymph Node Metastasis in Pelvis by CT Alone
NCT00416455 (15) [back to overview]The Diagnostic Sensitivity of PET/CT for Detection of Lymph Node Metastasis in Abdomen
NCT00416455 (15) [back to overview]Specificity for Detection of Lymph Node Metastasis in Combination of Abdomen and Pelvis by CT Alone
NCT00416455 (15) [back to overview]Percentage of Participants in Whom PET/CT Detects Biopsy-proven Disease Outside the Abdominal Lymph Nodes
NCT00416455 (15) [back to overview]Percentage of Participants in Whom PET/CT Detects Biopsy-proven Disease Outside the Pelvic Lymph Node
NCT00416455 (15) [back to overview]Sensitivity Between for Detection of Lymph Node Metastasis in Combination of Abdomen and Pelvis by CT Alone
NCT00416455 (15) [back to overview]The Diagnostic Specificity of PET/CT for Detection of Lymph Node Metastasis in Abdomen
NCT00416455 (15) [back to overview]Cervical Cancer Patients With Adverse Events (Grade 3 or Higher) at Least Possibly Attributed to Extra-peritoneal or Laparoscopic Abdominal and Pelvic Lymphadenectomy
NCT00416455 (15) [back to overview]The Diagnostic Sensitivity of PET/CT for Detection of Lymph Node Metastasis in Combination of Abdomen and Pelvis
NCT00537056 (9) [back to overview]Tumor Size by Computed Tomography (CT) Scan
NCT00537056 (9) [back to overview]Initial Tumor Size
NCT00537056 (9) [back to overview]Histopathology
NCT00537056 (9) [back to overview]Initial Comprehensive Metabolic Panel
NCT00537056 (9) [back to overview]Tumor Necrosis
NCT00537056 (9) [back to overview]Tumor Size by DCE Magnetic Resonance Imaging (MRI) Scan
NCT00537056 (9) [back to overview]F-18 FDG Tumor Uptake (SUV Max)
NCT00537056 (9) [back to overview]DCE MRI AUC Peak Flow
NCT00537056 (9) [back to overview]Adverse Events
NCT00559377 (4) [back to overview]Disease-free Survival (DFS)
NCT00559377 (4) [back to overview]Overall Survival (OS)
NCT00559377 (4) [back to overview]Relationship Between Ki67 and Regional FMISO Uptake in Tumor
NCT00559377 (4) [back to overview]Relationship Between Hypoxia-related IHC Biomarkers and Regional FMISO Uptake in Tumor
NCT00564733 (1) [back to overview]Overall Response Rate (Patients That Achieve a CR or PR)
NCT00590395 (1) [back to overview]Sensitivity and Specificity of FDG PET/CT and Tc99mHIDA in the Evaluation of Subjects Suspected of Cholecystitis
NCT00602043 (3) [back to overview]Number of Participants With Clinical Benefit
NCT00602043 (3) [back to overview]Time to Progression
NCT00602043 (3) [back to overview]Best Overall Response
NCT00729157 (5) [back to overview]To Determine the Biologic Effect of IV VEGF Trap on FDG Avidity After Four Cycles (Approximately 8 Weeks) of Therapy Through Pre- and Post-treatment FDG-PET Scans in Patients With Recurrent and/or Metastatic D-TC-FCO.
NCT00729157 (5) [back to overview]The Safety and Toxicity Profile of IV VEGF Trap in Patients With Recurrent and/or Metastatic TC-FCO
NCT00729157 (5) [back to overview]Effect of Thyroglobulin Concentration on Progression-free Survival
NCT00729157 (5) [back to overview]Progression-free Survival to Determine the 6-month Progression-free-survival (PFS) Rate
NCT00729157 (5) [back to overview]Radiographic Response Rate of Aflibercept in Patients With Recurrent and/or Metastatic Thyroid Cancer That Did Not Respond to Radioactive Iodine Therapy
NCT00735917 (4) [back to overview]Six Month Survival
NCT00735917 (4) [back to overview]Overall Survival
NCT00735917 (4) [back to overview]Progression-Free Survival
NCT00735917 (4) [back to overview]Confirmed Tumor Responses (Complete Response [CR] or Partial Response [PR])
NCT00775268 (10) [back to overview]Time to Progression
NCT00775268 (10) [back to overview]18F- Fluorothymidine (FLT) Uptake Within the Tumor(s) Between Baseline vs Completion of Therapy Scans
NCT00775268 (10) [back to overview]18F- Fluorothymidine (FLT) Uptake, Positron-emission Tomography (PET) Standard Uptake Value (SUV)Max in Malignant Residual Tumors Versus Benign Lesions After Therapy
NCT00775268 (10) [back to overview]18F-fluorodeoxyglucose (18FDG) Standardized Uptake Values (SUV) Estimated Maximum and Tumor: Blood Pool Ratio at 1-hour Post-injection
NCT00775268 (10) [back to overview]3'-Deoxy-3'-[18F]-Fluorothymidine (FLT) Dynamic Influx Parameter (Ki) Standardized Uptake Values (SUV) Estimated Maximum at 1- and 2-hours Post-injection
NCT00775268 (10) [back to overview]Tumor Uptake With Fluorothymidine (FLT) - Maximum Standard Uptake Value (SUVmax)
NCT00775268 (10) [back to overview]Tumor(s) Maximum Standard Uptake Value (SUVmax) at Baseline and at Mid-treatment (Post-2 Cycles) Scan
NCT00775268 (10) [back to overview]Tumor(s) Maximum Standard Uptake Value (SUVmax) at Baseline Scan and SUVmax After Completion Scan in Responders and Non-responders' Patients
NCT00775268 (10) [back to overview]Number of Participants With the Presence/Absence of Abnormal 18F- Fluorothymidine (FLT) Uptake, and Positive/Negative Biopsy
NCT00775268 (10) [back to overview]Number of Participants With Non-serious Adverse Events Assessed by the Common Terminology Criteria for Adverse Events (CTCAE v4.0)
NCT00794339 (14) [back to overview]Primary Tumor Recurrence
NCT00794339 (14) [back to overview]Relationship of Copper Cu 64-ATSM Uptake T/M Ratio and CA-IX Composite Score as a Marker of Tumor Hypoxia
NCT00794339 (14) [back to overview]Relationship of Copper Cu 64-ATSM Uptake T/M Ratio and CA-IX Staining Intensity Score: as a Marker of Tumor Hypoxia
NCT00794339 (14) [back to overview]Relationship of Copper Cu 64-ATSM Uptake T/M Ratio and Glucose Transporter 1 (GLUT1) Composite Score as a Marker of Tumor Hypoxia
NCT00794339 (14) [back to overview]Relationship of Copper Cu 64-ATSM Uptake T/M Ratio and Glucose Transporter 1 (GLUT1) Percentage of Tumor Cells Staining Score as a Marker of Tumor Hypoxia
NCT00794339 (14) [back to overview]Relationship of Copper Cu 64-ATSM Uptake T/M Ratio and Glucose Transporter 1 (GLUT1) Staining Intensity Score: as a Marker of Tumor Hypoxia
NCT00794339 (14) [back to overview]Relationship of Copper Cu 64-ATSM Uptake T/M Ratio and Vascular Endothelial Growth Factor (VEGF) Composite Score as a Marker of Tumor Hypoxia
NCT00794339 (14) [back to overview]Relationship of Copper Cu 64-ATSM Uptake T/M Ratio and Vascular Endothelial Growth Factor (VEGF) Staining Intensity Score: as a Marker of Tumor Hypoxia
NCT00794339 (14) [back to overview]Relationship of Copper Cu 64-ATSM Uptake T/M Ratio and VEGF Percentage of Tumor Cells Staining Score as a Marker of Tumor Hypoxia
NCT00794339 (14) [back to overview]Relationship Between Copper Cu 64-ATSM Uptake in the Primary Tumor and Progression-free Survival 3 Years After Chemoradiotherapy
NCT00794339 (14) [back to overview]Lymph Node Metastasis at Baseline
NCT00794339 (14) [back to overview]Copper Cu 64-ATSM T/M Uptake and Overall Survival
NCT00794339 (14) [back to overview]Relationship Between Copper Cu 64-ATSM Uptake and Development of Distant Metastasis
NCT00794339 (14) [back to overview]Relationship of Copper Cu 64-ATSM Uptake T/M Ratio and Carbonic Anhydrase IX (CA-IX) Percentage of Tumor Cells Staining Score as a Marker of Tumor Hypoxia
NCT00852644 (2) [back to overview]Participants Who Did Not Experience a Dose Limiting Toxicity in the Less Than 3 Centimeter Cohort
NCT00852644 (2) [back to overview]Participants Who Did Not Experience a Dose Limiting Toxicity in the More Than 3 Centimeter Cohort
NCT00906503 (1) [back to overview]Feasibility of Ultra Short-term Steroid Therapy to Increase the Accuracy of FDG-PET/CT Imaging
NCT00941070 (11) [back to overview]Progression Free Survival by Smoking Status
NCT00941070 (11) [back to overview]Progression Free Survival by HPV Subtype
NCT00941070 (11) [back to overview]Clinical and Objective Response Assignment
NCT00941070 (11) [back to overview]Clinical and Objective Response Assignment
NCT00941070 (11) [back to overview]Clinical and Objective Response Assignment
NCT00941070 (11) [back to overview]Percent of Patients With Incidence of Grade 2 or Higher Gastrointestinal and Genitourinary Toxicity, Assessed Using CTCAE v3.0 Until December 31, 2010 and CTCAE v4.0 Beginning January 1, 2011
NCT00941070 (11) [back to overview]PET/CT Scan Metabolic Activity
NCT00941070 (11) [back to overview]Change in Smoking Behavior, Assessed Using the Smoking Questionnaire and Cessation Counseling
NCT00941070 (11) [back to overview]Progression-free Survival
NCT00941070 (11) [back to overview]PET/CT Scan Metabolic Activity
NCT00941070 (11) [back to overview]Fasting F-18 Fluorodeoxyglucose (FDG) Positron Emission Tomography (PET/CT) Imaging Complete Metabolic Response, Reported Following National Cancer Institute (NCI) and European Organization for Research and Treatment of Cancer (EORTC) Guidelines.
NCT00963807 (5) [back to overview]Change in FLT Uptake in Responders and Non-responders
NCT00963807 (5) [back to overview]Overall Response Rate Reported as a Proportion of the Total Number of Patients Who Received at Least One Cycle of Therapy Assessed Using Response Evaluation Criteria in Solid Tumors (RECIST)
NCT00963807 (5) [back to overview]Change in FLT Uptake
NCT00963807 (5) [back to overview]Change in 18F-Fluorodeoxyglucose (FDG) Uptake
NCT00963807 (5) [back to overview]Change in 18F-Fluorothymidine (FLT) Uptake
NCT00971789 (1) [back to overview]Number of Participants With Adverse Events
NCT01004718 (1) [back to overview]Percentage Change in Maximum Lesional FDG Uptake From 60 to 180 Minutes After FDG Administration
NCT01038778 (8) [back to overview]Changes in the Level of Specific T Lymphocytes
NCT01038778 (8) [back to overview]Incidence of Toxicities
NCT01038778 (8) [back to overview]Dose-limiting Toxicities of Entinostat When Combined With Aldesleukin Within the Phase I
NCT01038778 (8) [back to overview]Time-to-tumor Progression
NCT01038778 (8) [back to overview]Incidence of Toxicity (Phase I)
NCT01038778 (8) [back to overview]Overall Response Rate (Complete Plus Partial) (Phase II)
NCT01038778 (8) [back to overview]Overall Survival
NCT01038778 (8) [back to overview]Progression-free Survival
NCT01129206 (4) [back to overview]Overall Response
NCT01129206 (4) [back to overview]Overall Survival (OS)
NCT01129206 (4) [back to overview]Progression-free Survival (PFS)
NCT01129206 (4) [back to overview]Correlation of FDG PET Response With Response Rate
NCT01132807 (3) [back to overview]36 Month Progression Free Survival Rate of Patients Receiving 4 Cycles of ABVD Versus Patients Receiving 2 Cycles of ABVD and 2 Cycles of BEACOPP and Radiation.
NCT01132807 (3) [back to overview]Complete Response Rate
NCT01132807 (3) [back to overview]Progression-Free Survival (PFS) at 36-Months for Patients Who Received 4 Cycles of ABVD
NCT01146054 (5) [back to overview]Evaluate Acute Gastrointestinal Toxicity up to 3 Months of Treatment.
NCT01146054 (5) [back to overview]To Evaluate Progression Free Survival Following Gemcitabine and SBRT for up to 5 Years of Follow up .
NCT01146054 (5) [back to overview]To Determine the Rate of (Grade 2 or Greater) Gastrointestinal Toxicity Attributable to Gemcitabine and Fractionated SBRT at One Year.
NCT01146054 (5) [back to overview]To Determine the Overall Survival in Pancreatic Cancer Patients Treated With Gemcitabine and SBRT for up to 5 Years of Follow up.
NCT01146054 (5) [back to overview]Proportion of Participants Achieving Freedom From Local Progression (FFLP) in Patients Treated With Gemcitabine Followed by Fractionated Stereotactic Body Radiotherapy (SBRT) for up to 5 Years of Follow up.
NCT01169350 (1) [back to overview]Changes From Baseline Hypoxic Volume (HV)
NCT01237054 (7) [back to overview]Comparison of Serum Angiogenic Marker Reverse Contrast Transfer Rate (Kep) Between MGUS and SMM/MM Groups
NCT01237054 (7) [back to overview]Comparison of Serum Angiogenic Markers Ang2 (Angiopoietin), G-CSF (Granulocyte-colony Stimulating Factor), Follistatin, HGF (Hepatocyte Growth Factor), FGF-1, Endothelin 1, and VEGF-A (Vascular Endothelial Growth Factor-A) Between MGUS and SMM/MM Groups
NCT01237054 (7) [back to overview]Count of Participants With Positive and Negative 18F-FDG PET CT and F18-NaF PET CT Imaging Results in Individuals With MGUS, SMM, and MM.
NCT01237054 (7) [back to overview]Count of Participants With Positive DCE-MRI Imaging Results
NCT01237054 (7) [back to overview]Comparison of Reverse Contrast Transfer Rate (Kep) and Forward Contrast Transfer Rate (Ktrans) Among Patients With MGUS, SMM, and MM
NCT01237054 (7) [back to overview]Comparison of Microvessel Density (MVD) Among Patients With MGUS, SMM, and MM
NCT01237054 (7) [back to overview]Comparison of Microvessel Density (MVD) Between MGUS and SMM/MM Groups
NCT01286272 (3) [back to overview]Complete Response Rate
NCT01286272 (3) [back to overview]Progression-free Survival (PFS)
NCT01286272 (3) [back to overview]The Number of Patients Who Experienced Grade 3+ Hematologic and Non-hematologic Adverse Events at Least Possibly Related to Treatment
NCT01359592 (4) [back to overview]Five-year Progression-free Survival (PFS) Rate in Patients With Newly Diagnosed Limited Stage Diffuse Large B-cell Lymphoma (DLBCL)
NCT01359592 (4) [back to overview]Number of Patients With Grade 3 Through Grade 5 Adverse Events That Are Related to Study Drug
NCT01359592 (4) [back to overview]Progression-free Survival (PFS) Within the PET+ and PET- Subgroups of Patients With Newly Diagnosed Limited-stage Diffuse Large B-Cell Lymphoma (DLBCL)
NCT01359592 (4) [back to overview]Overall Survival of Patients With Newly Diagnosed Limited-stage Diffuse Large B-Cell Lymphoma (DLBCL)
NCT01462630 (5) [back to overview]Response Rate Defined as Partial Response (PR)
NCT01462630 (5) [back to overview]Evaluation of Toxicity of Pazopanib Hydrochloride in This Patient Population
NCT01462630 (5) [back to overview]Overall Survival of Patients Treated With Pazopanib Hydrochloride
NCT01462630 (5) [back to overview]PFS Rate
NCT01462630 (5) [back to overview]Response Rate Defined as CR
NCT01720602 (5) [back to overview]Response Rate According to RECIST
NCT01720602 (5) [back to overview]Duration of Response
NCT01720602 (5) [back to overview]Rate of Clinical Benefit of Patients Receiving Vorinostat/AI Combination Therapy According to RECIST
NCT01720602 (5) [back to overview]Progression-free Survival (PFS)
NCT01720602 (5) [back to overview]Overall Survival
NCT01806675 (4) [back to overview]Change From Baseline in Maximum Standard Uptake Values (SUVmax)
NCT01806675 (4) [back to overview]Change in Tumor Size
NCT01806675 (4) [back to overview]Change From Baseline in Maximum Standard Uptake Values (SUVmax)
NCT01806675 (4) [back to overview]Tumor Response Rate by EORTC Criteria
NCT01807117 (11) [back to overview]SUVmax in Which the PET-CT Was Performed Prior to the PET-MRI.
NCT01807117 (11) [back to overview]True Positive Rate
NCT01807117 (11) [back to overview]True Negative Rate
NCT01807117 (11) [back to overview]SUVmax Ratio in Which the PET-MRI Was Performed Prior to the PET-CT
NCT01807117 (11) [back to overview]SUVmax Ratio in Which the PET-CT Was Performed Prior to the PET-MRI
NCT01807117 (11) [back to overview]SUVmax in Which the PET-MRI Was Performed Prior to the PET-CT
NCT01807117 (11) [back to overview]Negative Predictive Values for PET-CT and PET-MRI
NCT01807117 (11) [back to overview]Maximum Standardized Uptake Value (SUVmax) in Physiologic Regions and Fluorodeoxyglucose (FDG) Avid Lesions in Participants Where PET-CT Was Performed Prior to the PET-MRI
NCT01807117 (11) [back to overview]False Negative Rate
NCT01807117 (11) [back to overview]Proportion of Lesions Identified by PET-CT That Were Correctly Detected by PET-MRI
NCT01807117 (11) [back to overview]Positive Predictive Values for PET-CT and PET-MRI
NCT01821105 (3) [back to overview]All Adverse Events and Complications
NCT01821105 (3) [back to overview]Tumor Detection
NCT01821105 (3) [back to overview]Detection of Position Accuracy With Handheld Probe on Anatomical Location.
NCT01890343 (2) [back to overview]Quantitative Amyloid Image Assessment
NCT01890343 (2) [back to overview]Qualitative Amyloid Image Assessment
NCT01917136 (1) [back to overview]Changes in RV Function
NCT01931709 (6) [back to overview]Percent Change in PET K1 Between Mid-therapy and Pre-therapy FDG PET Scans and Its Association With Pathologic Response
NCT01931709 (6) [back to overview]Time of Surgery to Overall Survival
NCT01931709 (6) [back to overview]Time From Surgery to Breast Cancer Recurrence
NCT01931709 (6) [back to overview]Percent Change in Tumor Metabolism / Perfusion Ratio (MRFDG/K1) Between Mid-therapy and Pre-therapy FDG PET Scans and Its Association With Pathologic Response
NCT01931709 (6) [back to overview]Number of Participants With Favorable Pathologic Response at Surgery
NCT01931709 (6) [back to overview]Percent Change in DCE-MRI Peak Percent Enhancement (Peak PE) Between Mid-therapy and Pre-therapy Breast MRI Scans and Its Association With Pathologic Response
NCT02018107 (2) [back to overview]Does an Inadequate Ablation Margin on PET Predict Local Progression? Compare to MRI?
NCT02018107 (2) [back to overview]Number and Percentage of Tumors With Complete, Circumferential Ablation Margin Visibility During FDG PET/CT-guided Liver Ablations (AP-PET-1 v. Contrast-enhanced MRI)
NCT02149173 (4) [back to overview]Change in F-18 16 Alpha-fluoroestradiol (FES) Standardized Uptake Value (SUV), Assessed by a One-sample Test of the Percent Change in FES SUV
NCT02149173 (4) [back to overview]Proportion of Patients Experienced a Threshold in Percentage Change, or Surpassed a Targeted Follow-up F-18 16 Alpha-fluoroestradiol (FES) Standardized Uptake Value (SUV)
NCT02149173 (4) [back to overview]F-18 16 Alpha-fluoroestradiol (FES) Uptake
NCT02149173 (4) [back to overview]Time to Disease Progression
NCT02226276 (2) [back to overview]Relationship Between Tumor Minimum Uptake of Copper Cu 64-DOTA-trastuzumab as Measured by PET and Patient Best Response
NCT02226276 (2) [back to overview]Relationship Between Average Tumor Uptake of Copper Cu 64-DOTA-trastuzumab as Measured by PET and Patient Best Response
NCT02448225 (4) [back to overview]Uptake of 18F-FSPG (Expressed in Maximal Standardized Uptake Value [SUV] Within the Tumor)
NCT02448225 (4) [back to overview]Ability of 18F-FSPG PET/CT to Discriminate Benign From Malignant Nodules
NCT02448225 (4) [back to overview]Ability of 18F-FSPG PET/CT to Stage of Lung Cancer (Metastatic or Not)
NCT02448225 (4) [back to overview]CD44 and xC- Expression Levels in Tissue Samples(0-3)
NCT02810873 (1) [back to overview]Number of F-18-FDG Positive Lesions That Are Detected by the Copper Cu 64 TP3805 Analog
NCT02937168 (3) [back to overview]Number of Participants With Adverse Events (AEs)
NCT02937168 (3) [back to overview]Part 1: Average Global Lung Glycolysis (GLG) at Day 8
NCT02937168 (3) [back to overview]Part 1: Average Global Lung Glycolysis (GLG) at Baseline (Day 1)
NCT03125629 (2) [back to overview]PET/CT vs PET/MRI Difference in Standardized Uptake Value Max (SUVmax), by Radiotracer
NCT03125629 (2) [back to overview]Absolute Accuracy of SUV Max of PET/CT vs PET/MRI
NCT03226249 (3) [back to overview]Complete Response (CR) With Pembrolizumab Treatment Alone
NCT03226249 (3) [back to overview]Overall Survival at Treatment Completion
NCT03226249 (3) [back to overview]Progression Free Survival (PFS) at Treatment Completion
NCT03262389 (2) [back to overview]Visual Image Analysis of Detected Multiple Myeloma Lesions
NCT03262389 (2) [back to overview]Mean Multiple Myeloma Lesions Detected
NCT03320564 (1) [back to overview]Change in SUVpeak of Target Lesions Between Infiltrated and Non-infiltrated Scans
NCT03549598 (2) [back to overview]13NH3 PET/CT Uptake With Cardia Sarcoidosis (CS)
NCT03549598 (2) [back to overview]18FDG Uptake With Cardia Sarcoidosis (CS)
NCT04692103 (3) [back to overview]F-18 16 Alpha-fluoroestradiol (FES) Uptake
NCT04692103 (3) [back to overview]Proportion of Patients With a Threshold of Percentage Change, or That Surpass a Targeted Follow-up F-18 16 Alpha-fluoroestradiol (FES) Standardized Uptake Value (SUV)
NCT04692103 (3) [back to overview]Change in F-18 16 Alpha-fluoroestradiol (FES) Standardized Uptake Value (SUV) - Avg SULmax

Response

Standard response criteria will be used to assess the CT (computed tomography) scan images on a lesion per lesion basis. Complete response is complete disappearance of the index lesion on followup scan when compared to the pretreatment images. Partial response is a decrease of 50% or greater in the product of the perpendicular diameters of the measured lesion following treatment compared to the pretreatment images. Minor response is a decrease between 25% and 49% in the product of the perpendicular diameters of the measured lesion following treatment compared to the pretreatment images. Stable disease is no change in the size of the treated lesion. Progressive disease is an increase of greater than 25% in the product of the perpendicular diameters of the measured lesion following treatment compared to the pretreatment images. (NCT00019604)
Timeframe:

InterventionParticipants (Number)
Complete ResponsePartial ResponseMinor ResponseStable DiseaseProgressive Disease
Radiofrequency Ablation in Liver Cancer000023

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Number of Participants With Adverse Events

Here is the number of participants with adverse events. For a detailed list of adverse events see the adverse event module. (NCT00019604)
Timeframe: 9 years, 9 months

InterventionParticipants (Number)
Radiofrequency Ablation in Liver CancerNA

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Early Post Transplantation Relapse

Participants who experienced recurrence or progression of disease following transplant. (NCT00043979)
Timeframe: up to 300 days

InterventionDays (Median)
Arm 2-Recipients100

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Median Progression Free Survival

Progression free survival was based on the time from on-study date until progression or last follow-up. (NCT00043979)
Timeframe: up to 77 months

InterventionMonths (Median)
Arm 2-Recipients15.9

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Median Time to Reach a Platelet Count of 50,000/mm(3)

Days for participants to achieve a platelet count of 50,000/mm(3). (NCT00043979)
Timeframe: up to 43 days

InterventionDays (Median)
Arm 2-Recipients15

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Two Year Survival Rate for Patients Undergoing Allo-Hematopoietic Stem Cell Transplant

Participants who are alive at two years following Allo-Hematopoietic Stem Cell Transplant. (NCT00043979)
Timeframe: 2 years

Interventionpercentage of participants (Number)
From date of enrollmentFrom date of transplantation
Arm 2-Recipients39.134.8

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Median Time to Reach Absolute Neutrophil Count of 500/mm(3)

Days for participants to achieve a neutrophil count of 500/mm(3). (NCT00043979)
Timeframe: up to 12 days

InterventionDays (Median)
Arm 2-Recipients9

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Number of Participants Who Experienced Graft Versus Tumor Effect (GVT)

GVT is defined as tumor response after day 42 post-transplantation without cytotoxic therapy. (NCT00043979)
Timeframe: up to day 100

InterventionParticipants (Count of Participants)
Arm 2-Recipients0

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Number of Participants With Engraftment

Engraftment is defined as rapid conversion to complete donor chimerism and is assessed by blood counts and chimerism, >95% donor engraftment at day 100 in >75% of patients. (NCT00043979)
Timeframe: 100 days

InterventionParticipants (Number)
Arm 2-Recipients23

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Cluster of Differentiation 4 (CD4) Reconstitution

The median CD4 count with a range of 85-1565 (absolute count) was used to determine recovery and were considered recovered if in this range. The CD4 count was established by flow cytometry testing. (NCT00043979)
Timeframe: Day +28-42

Interventionmm(3) (Median)
Arm 2-Recipients284

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Toxicity

Here is the number of participants with adverse events. For a detailed list of adverse events see the adverse event module. (NCT00043979)
Timeframe: 16.5 months

InterventionParticipants (Number)
Arm 2-Recipients30

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Best Response Post-Hematopoietic Stem Cell Transplant EOCH (Etoposide, Vincristine, Cyclophosphamide, and Doxorubicin)

Response is defined by the Response Evaluation Criteria in Solid Tumors (RECIST). RECIST criteria offer a simplified, conservative, extraction of imaging data for wide application in clinical trials. They presume that linear measures are an adequate substitute for 2-D (dimensional) methods and registers four response categories: Complete response (CR) is disappearance of all target lesions. Partial response (PR) is 30% increase in the sum of the longest diameter of target lesions. Progressive disease (PD) is 20% increase in the sum of the longest diameter of target lesions. Stable disease (SD) is small changes that do not meet above criteria. For the purposes of this study very good partial response ((VGPR) is >75% reduction in disease) was also employed. (NCT00043979)
Timeframe: up to 10 cycles of therapy or 280 days

InterventionParticipants (Count of Participants)
Complete Response (CR)Progressive Disease (PD)Partial Response (PR)Very Good Partial Response (VGPR)
Arm 2-Recipients2442

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Median Survival From Date of Progression

Median survival from date of progression is based on the time from on-study date until progression or last follow-up. (NCT00043979)
Timeframe: up to 77 months

InterventionMonths (Median)
Participants who did not receive a transplant(n=7)Participants who received a transplant (n=23)
Arm 2-Recipients3.319.1

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Number of Participants to Complete Conversion to >95% Donor Chimerism

Participants who tolerated the transplantation regimen and accepted >95% of the donors blood, marrow, and/or tissue. (NCT00043979)
Timeframe: up to 30 days

InterventionParticipants (Count of Participants)
Day +14Day +28
Arm 2-Recipients2323

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Number of Participants With Acute and Chronic GVHD

Acute GVHD as by Modified Glucksberg Criteria occurring before day 100. Chronic GVHD as per Seattle criteria occurring after day 100. (NCT00043979)
Timeframe: up to 5 years or death

,
Interventionparticipants (Number)
acute GVHDchronic GVHD
Recipients -Cyclosporine GVHD Prophylaxis1212
Recipients -Tacrolimus/Sirolimus GVHD Prophylaxis55

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Post-Hematopoietic Stem Cell Transplant (HSCT) Radiotherapy

Site of radiotherapy (high energy radiation) and/or toxicity experienced by the participants post HSCT radiotherapy. Grading was preformed using the Modified Glucksberg Criteria. (NCT00043979)
Timeframe: up to 6 cycles or 168 days

InterventionParticipants (Count of Participants)
Chest wall; G2 skinAbdomen; G4 GIPancreas; G4 LFTs, G4 pancreatitisPleura, mediastinum; G4 LFTs, G2 mucositisChest wall; G4 skin, G3 mucositisSpine, skull; G2 nausea+vomiting, G2 fatiguePelvis; G4 enteritisPulmonary (cyberknife)Brain; B3 mucositisWhole lung; G3 mucositis, G3 skin, G5 lungL arm, R shoulder, B/L femur
Arm 2-Recipients11111111111

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Tumor Progression as Measured by Tumor Area and Volume at 1 Year.

We correlated SUVmax and change in tumor volume over the subsequent year (NCT00060008)
Timeframe: One year

Interventionpercentage of change (Median)
SUVmax < 24
SUVmax >227

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Histological Response Determined by FDG Uptake Correlates

"The primary objective was to demonstrate that a decrease in FDG-SUV discriminates treatment response. Response was defined pathologically based on microscopic inspection for residual cancer cells and fibrosis.~Using a two sample t-test, we would be able to adequately test that the decrease in SUV early in the treatment plan is significantly different between responders and non responders. Data adjudication was invalid, and needs to be re-adjudicated~Non-Responder= Tumor Regression Grade 3 or higher Responder=Tumor Regression Grade 1 (CR) or Grade 2 (PR)" (NCT00062374)
Timeframe: Day 15

Interventionparticipants (Number)
Progression of DiseaseRespondersNon-Responders
Arm I2338

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Disease Free Survival (DFS)

Overall Survival (OS) and Disease Free Survival (DFS) are the secondary endpoints. Technical problems with measurement of OS leading to unreliable or uniterpretable data. Data adjudication was invalid, and needs to be re-adjudicated. Therefore, only DFS data is being reported. (NCT00062374)
Timeframe: Every 3 mos for the first 2 yrs, then every 6 mos for 2 years and once a year afterwards, up to 5 years

Interventionmonths (Median)
Arm I23.8

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Frequency of Adverse Events According to National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE) Version 4.0

Summary of Adverse Events (AEs) by Maximum Grade where Grade 1 AEs >20%, Grade 2 AEs >10%, all Grade 3, Grade 4 and Grade 5 reported. (NCT00085293)
Timeframe: Up to 6 months

Interventionpercentage of participants (Number)
Grade 1, NauseaGrade 1, FatigueGrade 1, Oral MucositisGrade 1, Pharyngolaryngeal painGrade 1, Decreased white blood cellGrade 2, FatigueGrade 2, Decreased white blood cellGrade 2, Neutrophil count decreasedGrade 2, Lymphocyte count decreasedGrade 3, Decreased white blood cellGrade 3, Neutrophil count decreasedGrade 3, Febrile neutropeniaGrade 3, InfectionsGrade 3, respiratory disordersGrade 4, Decreased white blood cellGrade 5
Treatment4233252525252516164225888580

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Restoration of Radioiodine Uptake in Metastatic Lesions as Demonstrated by Diagnostic Whole-body Scanning After Decitabine Administration

"Number of participants with restoration of radioiodine responsiveness as determined by visible uptake on radioiodine scan in radiographically detectable metastatic foci of papillary or follicular thyroid carcinoma. Response to Decitabine defined as demonstration of radioiodine uptake determined by centralized blinded review of diagnostic scan. All who demonstrated radioiodine uptake in metastatic foci following decitabine therapy would then undergo thyroid hormone withdrawal and a second course of decitabine in preparation for therapeutic administration of radioiodine.~Diagnostic radioiodine scans following decitabine therapy (week 3) with a radioiodine scan following thyrotropin alfa stimulation, 0.9 mg intramuscular (IM) injection 24 and 48 hours before administration of the 131I for imaging. Whole body scans (WBS) performed using a gamma camera." (NCT00085293)
Timeframe: Week 3 following 2 weeks of Decitabine therapy

Interventionparticipants (Number)
Treatment0

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The Number of Participants With Adverse Events

"Here are the total number of participants with adverse events. For the detailed list of adverse events see the adverse event module.~The descriptions and grading scales found in the revised NCI Common Terminology Criteria for Adverse Events (CTCAE) version 3.0 will be utilized for adverse event reporting. For a detailed description see the link in the Protocol Link module." (NCT00088374)
Timeframe: 1 yr, 364 days

Interventionparticipants (Number)
Participants With VHL Associated Renal Tumors9

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Number of Patients in Whom Renal Tumors Could be Identified by Positron Emission Tomography (PET)Based on Fludeoxyglucose 18F (18FDG) Uptake

Images were acquired after the intravenous administration of 18FDG and H2015 and used to analyze glucose uptake and estimate blood flow. The parameter to be measured is SUV (standard uptake value(s)) and/or mL/min/gm. (NCT00088374)
Timeframe: Baseline and at 12 weeks

Interventionparticipants (Number)
Participants With VHL Associated Renal Tumors0

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Number of Participants With Flow Dynamics Measured by DCE MRI Within the Renal and Non-renal Tumor

Dynamic images will be acquired before and after the intravenous administration of 0.1 mmol/kg of Gadolinium Diethylene triamine pentaacetic acid (DTPA). Time activity curves will be generated over a period of ten minutes. The parameter to be measured is the forward contrast transfer rate (Ktrans), the reverse contrast transfer rate (Kep), and/or the extravascular extracellular space volume fraction (Ve). Flow dynamics are a measure of blood flow changes in the tumor and are determined using the parameters we had previously defined (Ktrans, Kep, etc.). (NCT00088374)
Timeframe: Baseline and during therapy (12 weeks)

Interventionparticipants with changes (Number)
Participants With VHL Associated Renal Tumors3

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Number of Participants With a Renal Tumor Response

Response is defined as the number of patients who experience a disease response (complete response (CR) or partial response (PR) of renal tumors)per RECIST criteria. CR is the disappearance of all target lesions. PR is at least a 20% decrease in the sum of the longest diameter (LD) of target lesions, taking as reference the baseline sum LD. See the protocol Link module for the full criteria if desired. (NCT00088374)
Timeframe: 12 weeks

Interventionparticipants (Number)
Participants With VHL Associated Renal Tumors0

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Number of Participants With a Non-renal Tumor Response

Number of patients who have a PR or CR of non-renal lesions (pancreatic tumors, pheochromocytomas, and hemangioblastomas). The effect of treatment on the lesions will be evaluated at baseline and at the time of restaging (12 weeks) per RECIST criteria. RECIST is defined as changes in only the largest diameter (unidimensional measurement) of the tumor lesions. Lesions are either measurable or non-measurable using the criteria. See the protocol Link module for the full criteria if desired. (NCT00088374)
Timeframe: Baseline and 12 weeks

Interventionparticipants (Number)
Participants With VHL Associated Renal Tumors0

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Positron Emission Tomography as a Predictor of Response Measured by the Decrease in Standard Uptake Variable (SUV) After 1 Course of Therapy

Number of Participants with Decrease in Standard Uptake Variable (SUV) After 1 Course of Therapy (NCT00227539)
Timeframe: Between days 18 and 22 prior to second chemotherapy infusion

InterventionParticipants (Count of Participants)
Neoadjuvant Therapy, PET Scan and Surgery11

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Safety of Neoadjuvant Chemotherapy

The number of patients that experienced a grade 3 or higher adverse event. (NCT00227539)
Timeframe: Up to 4 weeks after last dose of chemotherapy

InterventionParticipants (Count of Participants)
Neoadjuvant Therapy, PET Scan and Surgery10

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Efficacy of Neoadjuvant Chemotherapy as Measured by Radiologic Response Rate

The number of patients that had either a CR, PR or SD after the completion of chemotherapy. Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) for target lesions and assessed by MRI: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Progression, as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions; Stable Disease (SD), neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for disease progression. (NCT00227539)
Timeframe: Up to 4 weeks after last dose of chemotherapy

InterventionParticipants (Count of Participants)
Neoadjuvant Therapy, PET Scan and Surgery20

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Cohort 1 - 18F-NaF PET/CT vs 18F-FDG PET/CT

The medical value of 18F-sodium fluoride (NaF) positron emission tomography / computed tomography (PET/CT) vs 18F-fluorodeoxyglucose (FDG) positron emission tomography / computed tomography (PET/CT) was assessed on the basis of the radiation oncologist's medical assessment of image quality and detected extent of disease, for each participant diagnosed with osseous (skeletal) metastases. Per protocol, the data were collected and the outcome is reported for Cohort 1 only. The outcome is reported as the number of participants for whom the medical value of the image was superior for 18-NaF PET/CT compared to 18F-FDG PET/CT, the same between both scans, or inferior for 18-NaF PET/CT compared to 18F-FDG PET/CT. The outcome result is represented as a number without dispersion. (NCT00375830)
Timeframe: 30 days

InterventionParticipants (Count of Participants)
18F-NaF > 18F-FDG18F-NaF = 18F-FDG18F-NaF < 18F-FDG
Cohort 1 Pilot-WB-MRI & Combined 18F-NaF-CT/18F-FDG-PET Scans300

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Cohort 1 - NaF PET/CT vs 99mTc-MDP Bone Scintigraphy

"The medical value of 18F-sodium fluoride (NaF) positron emission tomography / computed tomography (PET/CT) vs 99mTc-methylene diphosphonate (MDP) bone scintigraphy was assessed on the basis of the radiation oncologist's medical assessment of image quality and detected extent of disease, for each participant. Per protocol, the data were collected and the outcome is reported for Cohort 1 only. The outcome is reported as the number of participants for whom the medical value of the image was superior for 18F-NaF vs 99mTc-MDP bone scintigraphy (18F-NaF > 99mTc-MDP), the same between both scans (18F-NaF = 99mTc-MDP), or inferior for 18F-NaF vs 99mTc-MDP bone scintigraphy (18F-NaF < 99mTc-MDP)." (NCT00375830)
Timeframe: 30 days

InterventionParticipants (Count of Participants)
18F-NaF > 99mTc-MDP18F-NaF = 99mTc-MDP18F-NaF < 99mTc-MDP
Cohort 1 Pilot-WB-MRI & Combined 18F-NaF-CT/18F-FDG-PET Scans1000

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Cohort 2 - 18F-NaF/18F-FDG PET/CT vs Whole-body MRI for Detection of Extraskeletal Lesions

"Sensitivity; positive predictive value (PPV); and accuracy for the detection of extraskeletal lesions was assessed for 18F-sodium fluoride (NaF) / 18F-fluorodeoxyglucose (FDG) positron emission tomography / computed tomography (PET/CT) and for whole body magnetic imaging resonance (WB-MRI).~Sensitivity is a percentage that defines the proportion of true positive participants with the disease in a total group of participants.~PPV is the probability that participants with a positive screening test truly have the disease.~Accuracy is the proportion of true results (both true positives and true negatives) among the total number of cases examined.~Per protocol, the data were collected and the outcome is reported for Cohort 2 only. Sensitivity, PPV, and accuracy are reported as a percentage, a number without dispersion. Higher numbers represent better detection." (NCT00375830)
Timeframe: 30 days

,
Interventionpercentage of particpants (Number)
SensitivityPositive predictive valueAccuracy
Cohort 2 - Combined 18F-NaF-CT/18F-FDG-PET Scan92.981.376.5
Cohort 2 - Whole Body-MRI Scan92.986.782.4

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Cohort 2 - 18F-NaF/18F-FDG vs 99mTc-MDP Bone Scintigraphy for Detection of Skeletal Lesions

Sensitivity and accuracy for the detection of skeletal lesions was assessed for 18F-sodium fluoride (NaF) / 18F-fluorodeoxyglucose (FDG) positron emission tomography / computed tomography (PET/CT) and for 99mTc-methylene diphosphonate (MDP) bone scintigraphy. Per protocol, the data were collected and the outcome is reported for Cohort 2 only. Sensitivity and accuracy are reported as a percentage, a number without dispersion. Higher numbers represent better detection. (NCT00375830)
Timeframe: 30 days

,
Interventionpercentage of participants (Number)
SensitivityAccuracy
Cohort 2 - 99mTc-MDP Bone Scintigraphy Scan64.665.9
Cohort 2 Combined 18F-NaF-CT/18F-FDG-PET Scan96.289.8

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Cohort 2 - 18F-NaF/18F-FDG vs Whole-body MRI for Detection of Skeletal Lesions

Sensitivity and accuracy for the detection of skeletal lesions was assessed for 18F-sodium fluoride (NaF) / 18F-fluorodeoxyglucose (FDG) positron emission tomography / computed tomography (PET/CT) and for whole body magnetic imaging resonance (WB-MRI). Per protocol, the data were collected and the outcome is reported for Cohort 2 only. Sensitivity and accuracy are reported as a percentage, a number without dispersion. Higher numbers represent better detection. (NCT00375830)
Timeframe: 30 days

,
Interventionpercentage of particpants (Number)
SensitivityAccuracy
Cohort 2 - Combined 18F-NaF-CT/18F-FDG-PET Scan96.289.8
Cohort 2 - WB-MRI Scan81.474.7

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Cohort 2 - Overall Sensitivity and Accuracy for 18F-NaF/18F-FDG vs Whole-body MRI

Overall sensitivity and accuracy for the detection of tumor lesions was assessed for 18F-sodium fluoride (NaF) / 18F-fluorodeoxyglucose (FDG) positron emission tomography / computed tomography (PET/CT) and for whole body magnetic imaging resonance (WB-MRI). Per protocol, the data were collected and the outcome is reported for Cohort 2 only. Sensitivity and accuracy are reported as a percentage, a number without dispersion. Higher numbers represent better detection. (NCT00375830)
Timeframe: 30 days

,
Interventionpercentage of participants (Number)
SensitivityAccuracy
Cohort 2 - Combined 18F-NaF-CT/18F-FDG-PET Scan95.787.6
Cohort 2 - Whole Body Magnetic Resonance Imaging (WB-MRI) Scan83.376.0

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Cohort 2 - Overall Sensitivity and Accuracy for 18F-NaF/18F-FDG vs Whole-body MRI/99mTc-MDP Bone Scintigraphy

Overall sensitivity and accuracy for the detection of tumor lesions was assessed for 18F-sodium fluoride (NaF) / 18F-fluorodeoxyglucose (FDG) positron emission tomography / computed tomography (PET/CT) and for 99mTc-methylene diphosphonate (MDP) bone scintigraphy. Per protocol, the data were collected and the outcome is reported for Cohort 2 only. Sensitivity and accuracy are reported as a percentage, a number without dispersion. Higher numbers represent better detection. (NCT00375830)
Timeframe: 30 days

,
Interventionpercentage of participants (Number)
SensitivityAccuracy
Cohort 2 Combined 18F-NaF-CT/18F-FDG-PET Scan95.787.6
Cohort 2 WB-MRI & 99mTc-MDP Bone Scintigraphy91.683.0

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Cohort 3 - Total Skeletal Lesions Identified, Tc-99m MDP WBBS vs 18F-NaF / 18F-FDG PET/MRI

Participants in Cohort 3 received 99mTc-methylene diphosphonate (MDP) whole-body bone scintigraphy (WBBS) and 18F-sodium fluoride (NaF) / 18F-fluorodeoxyglucose (FDG) positron emission tomography / magnetic imaging resonance (PET/MRI) scans. On the basis of the scans, the total number skeletal lesions identified in the participants was determined. The outcome is reported as the total number skeletal lesions identified by each scan methodology, a number without dispersion. (NCT00375830)
Timeframe: 30 days

Interventionlesions (Number)
Cohort 3 - 99mTc-methyl Diphosphonate (MDP) Bone Scan81
Cohort 3 - 18F-NaF / 18F-FDG PET/MRI140

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Cohort 3 - Skeletal Lesions Identified by 99mTc MDP WBBS vs 18F-NaF / 18F-FDG PET/MRI

Participants in Cohort 3 received 99mTc-methylene diphosphonate (MDP) whole-body bone scintigraphy (WBBS) and 18F-sodium fluoride (NaF) / 18F-fluorodeoxyglucose (FDG) positron emission tomography / magnetic imaging resonance (PET/MRI) scans. On the basis of the scans, participants with skeletal lesions were identified. The outcome is reported as the number of Cohort 3 participants for whom skeletal lesions were identified by each scan methodology, a number without dispersion. (NCT00375830)
Timeframe: 30 days

InterventionParticipants (Count of Participants)
Cohort 3 - 99mTc-methyl Diphosphonate (MDP) Bone Scan37
Cohort 3 - 18F-NaF / 18F-FDG PET/MRI45

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Progression-free Survival Hazard Ratio by VEGF-A Expression

The association of VEGF-A expression with progression-free survival will be investigated for those strata that have a sufficient number of participants with VEGF-A measurements. (NCT00381797)
Timeframe: From start of treatment until the earliest of progressive disease, death, second malignancy or off study

InterventionHazard Ratio (Number)
Low Grade Glioma0.091

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Progression-free Survival Hazard Ratio by Carbonic Anhydrase 9 (CA9) Expression

The association of CA9 expression with progression-free survival will be investigated for those strata that have a sufficient number of participants with CA9 measurements. (NCT00381797)
Timeframe: From start of treatment until the earliest of progressive disease, death, second malignancy or off study

InterventionHazard Ratio (Number)
Low Grade Glioma0.705

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Progression-free Survival Hazard Ratio by Hypoxia Inducible Factor-2alpha Expression

The association of hypoxia inducible factor-2alpha expression with progression-free survival will be investigated for those strata that have a sufficient number of participants with hypoxia inducible factor-2alpha measurements. The hazard ratio was reported for patients who had hypoxia inducible factor-2alpha expression. (NCT00381797)
Timeframe: From start of treatment until the earliest of progressive disease, death, second malignancy or off study

InterventionHazard Ratio (Number)
Low Grade Glioma1.36

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Correlation of the Change in Vascular Endothelial Growth Factor Receptor-2 (VEGF-R2) Expression in Peripheral Blood Mononuclear Cells (PBMC) From Baseline With the Change in Perfusion From Magnetic Resonance Imaging

Spearman correlation coefficient is used to measure the correlation of the changes in VEGF-R2 with the changes in perfusion ratios. The changes are calculated by values at Day 15 minus values at baseline for VEGF-2 in Section 17 above and perfusion in Section 18 above, respectively. The correlation coefficients are reported in each stratum separately. (NCT00381797)
Timeframe: Baseline and Day 15 (after 2 doses of Bevacizumab) of course 1

InterventionCorrelation Coefficient (Number)
High-grade Gliomas0.5
Brain Stem Tumors-0.50

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Progression-free Survival Hazard Ratio by VEGF-R2 Expression

The association of VEGF-R2 expression with progression-free survival will be investigated for those strata that have a sufficient number of participants with VEGF-R2 measurements. (NCT00381797)
Timeframe: From start of treatment until the earliest of progressive disease, death, second malignancy or off study

InterventionHazard Ratio (Number)
Low Grade Glioma0.632

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Sustained Disease Stabilization Rate Associated With Bevacizumab and Irinotecan in Patients With Recurrent or Progressive Low-grade Glioma (Stratum E)

Disease stabilization is defined as a complete response(CR) or partial response(PR) observed during the first four courses and sustained for 8 weeks; or stable disease (SD) sustained for 6 courses characterized by SD at the end of course 2, at the end of course 4 and at the end of course 6. CR is complete disappearance of all enhancing tumor. PR is >= 50% reduction in tumor size. SD is at least stable and maintenance corticosteroid dose not increased in neurologic examination. (NCT00381797)
Timeframe: From day 1 of treatment up to 24 weeks

Interventionparticipants (Number)
Low Grade Glioma23

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Systemic Clearance

"Blood specimens were collected on the days listed for pharmacokinetic studies for Bevacizumab. These specimens were analyzed to produce steady-state plasma Bevacizumab concentration-time data in study participants. The concentration-time data were analyzed to provide an estimate of the systemic clearance. The data were collected but the analyses of the PK data were conducted by Genentech using a broader cohort of pediatric patients from multiple trials in the paper Bevacizumab dosing strategy in paediatric cancer patients based on population pharmacokinetic analysis with external validation published by British Journal of Clinical Pharmacology, 2016 volume 81(1):148-160. The estimates of the systemic clearance were calculated by the model described in the paper." (NCT00381797)
Timeframe: Baseline, Course 1 Day 1, Course 1 Day 15, Course 2 Day 1, Course 3 Day 1, Course 4 Day 1, and Course 5 Day 1

Interventionml/h (Mean)
Combined All Strata9.43

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Terminal Half-life

"Blood specimens were collected on the days listed for pharmacokinetic studies for Bevacizumab. These specimens were analyzed to produce steady-state plasma Bevacizumab concentration-time data in study participants. The concentration-time data were analyzed to provide an estimate of the PK parameters. The data were collected but the analyses of the PK data were conducted by Genentech using a broader cohort of pediatric patients from multiple trials in the paper Bevacizumab dosing strategy in paediatric cancer patients based on population pharmacokinetic analysis with external validation published by British Journal of Clinical Pharmacology,2016 volume 81(1):148-160. The estimates of the terminal half-life were calculated by the method described in the paper." (NCT00381797)
Timeframe: Baseline, Course 1 Day 1, Course 1 Day 15, Course 2 Day 1, Course 3 Day 1, Course 4 Day 1, and Course 5 Day 1

Interventionhours (Mean)
Combined All Strata125.2

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Volume of Distribution

"Blood specimens were collected on the days listed for pharmacokinetic studies for Bevacizumab. These specimens were analyzed to produce steady-state plasma Bevacizumab concentration-time data in study participants. The concentration-time data were analyzed to provide an estimate of the volume of distribution. The data were collected but the analyses of the PK data were conducted by Genentech using a broader cohort of pediatric patients from multiple trials in the paper Bevacizumab dosing strategy in paediatric cancer patients based on population pharmacokinetic analysis with external validation published by British Journal of Clinical Pharmacology ,2016 volume 81(1):148-160. The estimates of the volume of distribution were calculated by the model described in the paper." (NCT00381797)
Timeframe: Baseline, Course 1 Day 1, Course 1 Day 15, Course 2 Day 1, Course 3 Day 1, Course 4 Day 1, and Course 5 Day 1

Interventionml (Mean)
Combined All Strata1729

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Association of Log-transformed Tumor Diffusion Ratio With Progression-free Survival (PFS) Using Hazard Ratio Estimates

Using Cox Proportional Hazards Models, the association of tumor diffusion ratios with progression-free survival will be investigated. Magnetic resonance (MR) diffusion imaging is performed to investigate surrogate markers of tumor growth. Tumor diffusion ratios were longitudinal. As we are not comparing the strata or study arms, analyses will be done in each stratum separately, and thus we cannot report the Cox model results in the Statistical Analysis section. And we consider these estimates 'descriptive' within each stratum. In this analysis, the hazard ratio is a relative measure of likelihood that a study participant experiences the event of interest compared to another participant who has a one-unit lower Log-transformed tumor diffusion ratio. The Cox survival model provides the mean hazard ratio along with its 95% confidence interval, which we report below. (NCT00381797)
Timeframe: From start of treatment until the earliest of progressive disease, death, second malignancy or off study

InterventionHazard Ratio (Mean)
High-grade Gliomas4.41
Brain Stem Tumors1.82

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Association of Log-transformed Tumor Enhancing Volume With Progression-free Survival (PFS) Using Hazard Ratio Estimates

Using Cox Proportional hazards Models, the association of Log-transformed tumor enhancing volume with progression-free survival will be investigated. Volumetric magnetic resonance (MR) imaging is performed to investigate surrogate markers of tumor growth. Tumor enhancing volumes were longitudinal. As we are not comparing the strata or study arms, analyses will be done in each stratum separately, and thus we cannot report the Cox model results in the Statistical Analysis section and we consider these estimates 'descriptive' within each stratum. In this analysis, the hazard ratio is a relative measure of likelihood that a study participant experiences the event of interest compared to another participant who has a one-unit lower Log-transformed tumor enhancing volume. The Cox survival model provides the mean hazard ratio along with its 95% confidence interval, which we report below. (NCT00381797)
Timeframe: From start of treatment until the earliest of progressive disease, death, second malignancy or off study, OR up to 2 years

InterventionHazard Ratio (Mean)
High-grade Gliomas1.65
Brain Stem Tumors1.16

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Association of Log-transformed Tumor Volume Based on FLAIR With Progression-free Survival (PFS) Using Hazard Ratio Estimates

Using Cox proportional hazards models, the association of tumor volume based on FLAIR images with PFS will be investigated for those strata that have a sufficient number of participants with volume FLAIR measurements. Volumetric magnetic resonance imaging is performed to investigate surrogate markers of tumor growth. Volume FLAIR measurements were longitudinal. As we are not comparing the strata, analyses will be done in each stratum separately, and thus we cannot report the Cox model results in the Statistical Analysis section. We consider these estimates 'descriptive' within each stratum. In this analysis, the hazard ratio is a relative measure of likelihood that a study participant experiences the event of interest compared to another participant who has a one-unit lower Log-transformed tumor volume based on FLAIR. The Cox survival model provides the mean hazard ratio along with its 95% confidence interval, which we report below. (NCT00381797)
Timeframe: From start of treatment until the earliest of progressive disease, death, second malignancy or off study OR up to 2 years

InterventionHazard Ratio (Mean)
High-grade Gliomas1.47
Brain Stem Tumors1.76

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Association of Log-transformed Volume of Cystic Necrosis With Progression-free Survival (PFS) Using Hazard Ratio Estimates

Using Cox Proportional Hazards Models, the association of cystic necrosis with progression-free survival will be investigated. Volumetric magnetic resonance (MR) imaging is performed to investigate surrogate markers of tumor growth. Volumes of cystic necrosis were longitudinal. As we are not comparing the strata or study arms, analyses will be done in each stratum separately, and thus we cannot report the Cox model results in the Statistical Analysis section and we consider these estimates 'descriptive' within each stratum. In this analysis, the hazard ratio is a relative measure of likelihood that a study participant experiences the event of interest compared to another participant who has a one-unit lower Log-transformed tumor volume based on cystic necrosis. The Cox survival model provides the mean hazard ratio along with its 95% confidence interval, which we report below. (NCT00381797)
Timeframe: From start of treatment until the earliest of progressive disease, death, second malignancy or off study, OR up to 2 years

InterventionHazard Ratio (Mean)
High-grade Gliomas2.56
Brain Stem Tumors1.09

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Change in Diffusion Ratio Between the Baseline and Day 15 Brain Image

Diffusion ratio obtained from magnetic resonance (MR) diffusion imaging may explain changes in the tumor after therapy. Changes in the diffusion ratio will be reported for those strata that have a sufficient number of participants with MR diffusion imaging. The change was calculated from diffusion ratio at Baseline to diffusion ratio at Day 15 (values of diffusion ratio at Day 15 -values of diffusion ration at baseline). The higher of diffusion ratio is better. MR diffusion ratio is the diffusion solid part of tumor divided by the diffusion frontal white matter. There is no a unit available. (NCT00381797)
Timeframe: Baseline and day 15

InterventionRatio (Median)
High-grade Gliomas-0.34
Brain Stem Tumors-0.17
Ependymoma0.11
Low Grade Glioma-0.11

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Change in Perfusion Ratio Between the Baseline and Day 15 Brain Imaging

"Perfusion ratio obtained from magnetic resonance(MR) diffusion imaging may explain changes in the tumor after therapy. Changes in the perfusion ratio will be reported for those strata that have a sufficient number of participants with MR diffusion imaging. The change was calculated from perfusion ratio at Baseline to perfusion ratio at Day 15(values of perfusion ratio at Day 15 - values of perfusion ratio at baseline). The higher of perfusion ratio is worse.~MR perfusion ratio is perfusion solid part of tumor from CBV divided by perfusion frontal while matter. There is no a unit available." (NCT00381797)
Timeframe: Baseline and day 15

InterventionRatio (Median)
High-grade Gliomas-0.14
Brain Stem Tumors-1.98
Low Grade Glioma-0.42

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Change in Vascular Endothelial Growth Factor Receptor-2 (VEGF-R2) Expression in Peripheral Blood Mononuclear Cells (PBMC) From Baseline to Day-15

The change in VEGF-R2 was calculated from baseline to the time of the 2nd dose (values of 24-48 hours after the 2nd dose at Day 15 - values of pre-dose 1 Day1, i.e., baseline). VEGF-R2 is measured in the relative phosphorylation score which is generated as a ratio of normalized phosphorylated VEGF-R2 versus normalized total VEGF-R2 protein. (NCT00381797)
Timeframe: Baseline and 24-48 hours after the 2nd dose of Bevacizumab in course 1

InterventionRatio (Median)
High-grade Gliomas-0.37
Brain Stem Tumors-0.21
Medulloblastoma-0.003
Ependymoma0.24
Low Grade Glioma1.70

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Cumulative Incidence of Sustained Objective Responses

Cumulative incidence of sustained objective response provides a percentage of participants experiencing the event of interest at a given follow-up time point (for example, 6-months, 1-year, etc.) in the presence of competing events such as progressive disease or death, and it is estimated using the event data for both the event of interest and the competing events experienced by the study participants. In this sense, it is different than the incidence rates estimated in epidemiological studies in terms of 'incidences per 1000 person years. 6-month Cumulative incidence of sustained objective responses will be reported separately for each stratum. (NCT00381797)
Timeframe: From the first imaging after treatment up to 2 years

InterventionPercentage of Participants (Number)
High-grade Gliomas0
Brain Stem Tumors0
Medulloblastoma0
Ependymoma0
Low Grade Glioma0.058

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Descriptive Statistics for the Change of Perfusion in Magnetic Resonance Imaging Concurrently Measured With the Change in Vascular Endothelial Growth Factor Receptor-2 (VEGF-R2) Expression in Peripheral Blood Mononuclear Cells (PBMC)

The change of perfusion in magnetic resonance imaging is calculated by taking the difference between the Day-15 measurements and the Baseline measurements for patients who had the changes of VEGF-R2. The purpose of reporting the descriptive statistics is to provide the information for the correlation coefficients reported in the next section, Section 19. MR perfusion ratio is the ratio of the perfusion measurements in the tumor and the perfusion measurerement in comparative frontal while matter, which is the comparative healthy part of the brain. (NCT00381797)
Timeframe: Baseline and Day 15 (after 2 doses of Bevacizumab) of course 1

InterventionRatio (Mean)
High-grade Gliomas-1.60
Brain Stem Tumors-1.54

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Descriptive Statistics for the Changes in Vascular Endothelial Growth Factor Receptor-2 (VEGF-R2) Expression in Peripheral Blood Mononuclear Cells (PBMC) Concurrently Measured With the Changes in Perfusion From Magnetic Resonance Imaging

The changes in VEGF-R2 are calculated by values at Day 15 minus values at baseline for the patients who had the changes in perfusion from magnetic resonance perfusion imaging. The purpose of reporting descriptive statistics of changes of VEGF-R2 is to provide the information for the correlation coefficients in Section 19. (NCT00381797)
Timeframe: Baseline and Day 15 (after 2 doses of Bevacizumab) of course 1

InterventionRatio (Mean)
High-grade Gliomas-1.12
Brain Stem Tumors-1.20

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Number of Patients With High Carbonic Anhydrase 9 Expression at Baseline

The expression of Hypoxia inducible factor-2α, carbonic anhydrase IX (CA9), VEGF-A, and VEGF-R2 will be estimated by immunohistochemistry of paraffin sections in the medulloblastoma,ependymoma and low grade glioma strata. Reported separately for each stratum. (NCT00381797)
Timeframe: Baseline

Interventionparticipants (Number)
Medulloblastoma0
Ependymoma4
Low Grade Glioma2

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Number of Patients With High Hypoxia Inducible Factor-2alpha Expression at Baseline

The expression of Hypoxia inducible factor-2α, carbonic anhydrase IX (CA9), VEGF-A, and VEGF-R2 will be estimated by immunohistochemistry of paraffin sections in the medulloblastoma,ependymoma and low grade glioma strata. Reported separately for each stratum. (NCT00381797)
Timeframe: Baseline

Interventionparticipants (Number)
Medulloblastoma0
Ependymoma3
Low Grade Glioma7

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Number of Patients With High VEGF-A Expression at Baseline

The expression of Hypoxia inducible factor-2α, carbonic anhydrase IX (CA9), VEGF-A, and VEGF-R2 will be estimated by immunohistochemistry of paraffin sections in the medulloblastoma,ependymoma and low grade glioma strata. Reported separately for each stratum. (NCT00381797)
Timeframe: Baseline

Interventionparticipants (Number)
Medulloblastoma2
Ependymoma5
Low Grade Glioma16

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Number of Patients With High VEGF-R2 Expression at Baseline

The expression of Hypoxia inducible factor-2α, carbonic anhydrase IX (CA9), VEGF-A, and VEGF-R2 will be estimated by immunohistochemistry of paraffin sections in the medulloblastoma,ependymoma and low grade glioma strata. Reported separately for each stratum. (NCT00381797)
Timeframe: Baseline

Interventionparticipants (Number)
Medulloblastoma4
Ependymoma4
Low Grade Glioma13

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Objective Response Rate Sustained for ≥ 8 Weeks

Objective response is either a complete response or a partial response observed during the first four courses of treatment and sustained for 8 weeks. The objective response rate will be reported separately for patients with recurrent/progressive malignant glioma(Stratum A), recurrent/progressive instrinsic brain stem tumors(Stratum B), recurrent/progressive medulloblastoma(Stratum C), and recurrent/progressive ependymoma(Stratum D). CR is complete disappearance of all enhancing tumor. PR is >= 50% reduction in tumor size. This outcome measures is not defined for the Stratum E in the protocol. (NCT00381797)
Timeframe: From day 1 of treatment up to 24 weeks

Interventionparticipants (Number)
High-grade Gliomas0
Brain Stem Tumors0
Medulloblastoma0
Ependymoma0

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Progression-free Survival

Progression-Free survival is the interval of time between of protocol treatment and minimum date of documentation of progressive Disease,second malignancy,death due to any cause, or date of last follow-up. Progressive neurologic abnormalities or worsening neurologic status not explained by causes unrelated to tumor progression,OR the appearance of new tumor OR a > 25% increase in the sum of the products of two longest perpendicular diameters of all measurable tumors. K-M method was used to estimate progression-free survival. (NCT00381797)
Timeframe: From start of treatment up to 2 years

InterventionMonths (Median)
High-grade Gliomas4.20
Brain Stem Tumors2.35
Medulloblastoma2.48
Ependymoma2.15

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The Diagnostic Specificity of PET/CT for Detection of Lymph Node Metastasis in Pelvis

The specificity is defined as the percentage of patients who test without lymph node metastases in pelvis by pre-operative PET/CT among the patients who do not have lymph node metastases in pelvis identified by post-surgery pathology. The reported specificity is reader-averaged specificity. (NCT00416455)
Timeframe: Before surgery (FDG-PET/CT) and after surgery (pathology)

Interventionpercentage of participants (Mean)
Cervical Cancer Patients63
Endometrial Cancer Patients93

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Specificity for Detection of Lymph Node Metastasis in Abdomen by CT Alone

The specificity is defined as the percentage of patients who test without lymph node metastases by pre-operative CT alone among the patients who do not have lymph node metastases identified by post-surgery pathology in pelvis. The reported estimate of specificity is reader-average specificity across all 7 experienced PET-CT readers. (NCT00416455)
Timeframe: Before surgery (FDG-PET/CT) and after surgery (pathology)

Interventionpercentage of participants (Mean)
Cervical Cancer Patients89
Endometrial Cancer Patients93

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The Diagnostic Sensitivity of PET/CT for Detection of Lymph Node Metastasis in Pelvis

The sensitivity is defined as the percentage of patients who test with lymph node metastases by pre-operative PET/CT among the patients who have lymph node metastases identified by post-surgery pathology in pelvis. The reported sensitivity is reader-averaged sensitivity. (NCT00416455)
Timeframe: Before surgery (DCT) and after surgery (pathology)

Interventionpercentage of participants (Mean)
Cervical Cancer Patients83
Endometrial Cancer Patients65

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Sensitivity for Detection of Lymph Node Metastasis in Abdomen by CT Alone

The sensitivity is defined as the percentage of patients who test with lymph node metastases by pre-operative CT alone among the patients who have lymph node metastases identified by post-surgery pathology in abdomen. The reported estimate of sensitivity is reader-average sensitivity across all 7 experienced PET-CT readers. (NCT00416455)
Timeframe: Before surgery (FDG-PET/CT) and after surgery (pathology)

Interventionpercentage of participants (Mean)
Cervical Cancer Patients - Sensitivity of CT42
Endometrial Cancer Cohort - Sensitivity of CT50

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The Diagnostic Specificity of PET/CT for Detection of Lymph Node Metastasis in Combination of Abdomen and Pelvis

The specificity is defined as the percentage of patients who test without lymph node metastases by pre-operative PET/CT among the patients who do not have lymph node metastases identified by post-surgery pathology in combination of abdomen and pelvis. The reported specificity is reader-averaged specificity. (NCT00416455)
Timeframe: Before surgery (FDG-PET/CT) and after surgery (pathology)

Interventionpercentage of participants (Mean)
Cervical Cancer Patients69
Endometrial Cancer Patients83

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Specificity Between for Detection of Lymph Node Metastasis in Pelvis by CT Alone

The specificity is defined as the percentage of patients who test without lymph node metastases by pre-operative byCT alone among the patients who do not have lymph node metastases identified by post-surgery pathology in pelvis. The reported estimate of specificity is reader-average specificity across all 7 experienced PET-CT readers. (NCT00416455)
Timeframe: Before surgery (FDG-PET/CT) and after surgery (pathology)

Interventionpercentage of participants (Mean)
Cervical Cancer Patients62
Endometrial Cancer Patients89

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Sensitivity for Detection of Lymph Node Metastasis in Pelvis by CT Alone

The sensitivity is defined as the percentage of patients who test with lymph node metastases by pre-operative either CT alone among the patients who have lymph node metastases identified by post-surgery pathology in pelvis. The reported estimate of sensitivity is reader-average sensitivity across all 7 experienced PET-CT readers. (NCT00416455)
Timeframe: Before surgery (FDG-PET/CT) and after surgery (pathology)

Interventionpercentage of participants (Mean)
Cervical Cancer Patients - Sensitivity of CT79
Endometrial Cancer Cohort - Sensitivity of CT48

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The Diagnostic Sensitivity of PET/CT for Detection of Lymph Node Metastasis in Abdomen

The sensitivity is defined as the percentage of patients who test with lymph node metastases by pre-operative PET/CT among the patients who have lymph node metastases identified by post-surgery pathology in abdomen. The reported sensitivity is reader average sensitivity by seven experienced PET-CT readers. (NCT00416455)
Timeframe: Before surgery (FDG-PET-CT) and after surgery (pathology)

Interventionpercentage of participants (Mean)
Cervical Cancer Patients50
Endometrial Cancer Patients65

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Specificity for Detection of Lymph Node Metastasis in Combination of Abdomen and Pelvis by CT Alone

The specificity is defined as the percentage of patients who test without lymph node metastases by pre-operative CT alone among the patients who do not have lymph node metastases identified by post-surgery pathology in pelvis. The reported estimate of specificity is reader-average specificity across all 7 experienced PET-CT readers. (NCT00416455)
Timeframe: Before surgery (FDG-PET/CT) and after surgery (pathology)

Interventionpercentage of participants (Mean)
Cervical Cancer Patients63
Endometrial Cancer Patients85

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Percentage of Participants in Whom PET/CT Detects Biopsy-proven Disease Outside the Abdominal Lymph Nodes

(NCT00416455)
Timeframe: Before surgery (FDG-PET/CT) and after surgery (pathology)

Interventionpercentage of participants (Number)
Cervical Cancer Patients9
Endometrial Cancer Patients10

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Percentage of Participants in Whom PET/CT Detects Biopsy-proven Disease Outside the Pelvic Lymph Node

(NCT00416455)
Timeframe: Before surgery (FDG-PET/CT) and after surgery (pathology)

Interventionpercentage of participants (Number)
Cervical Cancer Patients10
Endometrial Cancer Patients6

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Sensitivity Between for Detection of Lymph Node Metastasis in Combination of Abdomen and Pelvis by CT Alone

The sensitivity is defined as the percentage of patients who test with lymph node metastases by pre-operative by CT alone among the patients who have lymph node metastases identified by post-surgery pathology in pelvis. The reported estimate of sensitivity is reader-average sensitivity across all 7 experienced PET-CT readers. (NCT00416455)
Timeframe: Before surgery (FDG-PET/CT) and after surgery (pathology)

Interventionpercentage of participants (Mean)
Cervical Cancer Patients-Sensitivity of CT77
Endometrial Cancer Patients54

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The Diagnostic Specificity of PET/CT for Detection of Lymph Node Metastasis in Abdomen

The specificity is defined as the percentage of patients who test without lymph node metastases by pre-operative PET/CT among the patients who do not have lymph node metastases identified by post-surgery pathology in abdomen. The reported specificity is reader average specificity by seven experienced PET-CT readers. (NCT00416455)
Timeframe: Before surgery (FDG-PET/CT) and after surgery (pathology)

Interventionpercentage of participants (Mean)
Cervical Cancer Patients85
Endometrial Cancer Patients88

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Cervical Cancer Patients With Adverse Events (Grade 3 or Higher) at Least Possibly Attributed to Extra-peritoneal or Laparoscopic Abdominal and Pelvic Lymphadenectomy

Number of participants with cervical cancer and a maximum grade of 3 or higher during treatment period. Adverse events are graded and categorized using CTCAE v3.0. (NCT00416455)
Timeframe: During surgery and up to 30 days after surgery.

InterventionParticipants (Count of Participants)
LeukopeniaThrombocytopeniaAnemiaOther HematologicDermatologicGastrointestinalInfectionLymphaticsMetabolicMusculoskeletalPainVascular
Number of Participants With a Maximum Grade of 3 or Higher Dur117114953123

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The Diagnostic Sensitivity of PET/CT for Detection of Lymph Node Metastasis in Combination of Abdomen and Pelvis

The sensitivity is defined as the percentage of patients who test with lymph node metastases by pre-operative PET/CT among the patients who have lymph node metastases identified by post-surgery pathology in combination of abdomen and pelvis. The reported sensitivity is reader-average sensitivity. (NCT00416455)
Timeframe: Before surgery (FDG-PET/CT) and after surgery (pathology)

InterventionPercentage of participants (Mean)
Cervical Cancer Patients81
Endometrial Cancer Patients63

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Tumor Size by Computed Tomography (CT) Scan

Tumor size was measured based on computed tomography (CT) pre- and post-sunitinib therapy. CT was performed immediately prior to the PET scan and is used to determine both the PET scan imaging area and PET image attenuation correction (AC). F-18 FDG PET provides the metabolic and physiologic data while CT provides the anatomical data. (NCT00537056)
Timeframe: 12 weeks

InterventionParticipants (Count of Participants)
F-18 FDG PET/CT and DCE MRINA

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Initial Tumor Size

Initial tumor size was measured using values obtained from computed tomography (CT) pre-sunitinib therapy. CT is performed immediately prior to the PET scan and is used to determine both the PET scan imaging area and PET image attenuation correction (AC). F-18 FDG PET provides the metabolic and physiologic data while CT provides the anatomical data. (NCT00537056)
Timeframe: pre-sunitinib therapy

InterventionParticipants (Count of Participants)
F-18 FDG PET/CT and DCE MRINA

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Histopathology

Histopathologic findings were correlated to the pre-treatment 18F-fluorodeoxyglucose positron emission tomography (F-18 FDG PET/CT) scan. Outcome is reported as the number of participants for whom both histopathology and F-18 FDG PET/CT indicated that active cancers was present. (NCT00537056)
Timeframe: 1 day

InterventionParticipants (Count of Participants)
F-18 FDG PET/CT and DCE MRI17

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Initial Comprehensive Metabolic Panel

A comprehensive metabolic panel is a blood test that measures sugar (glucose) level, electrolyte and fluid balance, kidney function, and liver function. It was performed prior to the administration of gadolinium contrast. For patients with normal renal function, approximately 90% of gadolinium contrast is excreted through the urinary system. These patients have known renal cell carcinoma, so it was important to perform a metabolic function panel prior to gadolinium injection, specifically to determine kidney function. Reported as the number of patients for whom the initial comprehensive metabolic panel was within institutional standards. (NCT00537056)
Timeframe: Prior to baseline DCE MRI

InterventionParticipants (Count of Participants)
F-18 FDG PET/CT and DCE MRI17

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Tumor Necrosis

The degree of tumor necrosis was measured using values obtained from dynamic contrast enhanced magnetic resonance imaging (DCE MRI) pre- and post-sunitinib therapy. Gadolinium contrast material given intravenously during the DCE MRI scan is used to improve visualization of blood vessels, tumors, and/or organs. (NCT00537056)
Timeframe: 12 weeks

InterventionParticipants (Count of Participants)
F-18 FDG PET/CT and DCE MRINA

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Tumor Size by DCE Magnetic Resonance Imaging (MRI) Scan

Tumor size was measured using values obtained from DCE MRI pre- and post-sunitinib therapy. Gadolinium contrast material given intravenously during the DCE MRI scan is used to improve visualization of blood vessels, tumors, and/or organs. (NCT00537056)
Timeframe: 12 weeks

InterventionParticipants (Count of Participants)
F-18 FDG PET/CT and DCE MRINA

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F-18 FDG Tumor Uptake (SUV Max)

"The maximum standardized uptake value (SUVmax) is a measurement of tumor metabolism as determined by the PET scan before and after 12-weeks of sunitinib therapy. Decreased SUVmax correlates to a reduction of tumor metabolism. Increased SUVmax correlates to an increase in tumor metabolism.~Reduction or increased SUVmax will be determined as the change from baseline in uptake of F18 FDG.~Results were based on the European Organization for Research and Treatment of Cancer (EORTC) for predicting progression free survival. EORTC criteria is a ± 25% change of SUVmax for assessment of progressive disease, stable disease and partial response." (NCT00537056)
Timeframe: 12 weeks minus baseline

InterventionSUVmax (Mean)
Baseline SUVmaxMean SUVmax, progression-free survivalSUVmax, progression/relapse
F-18 FDG PET/CT and DCE MRI9.8-18.934.0

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DCE MRI AUC Peak Flow

Area under the curve (AUC) was measured using receiver operating characteristic (ROC) curve analysis. ROC curve analysis measures sensitivity (true-positives, correctly diagnosed positive pathologies) against specificity (true-negatives, correctly diagnosed negative pathologies or free of disease) of the DCE MRI scan. An area of 1.0 under the curve would equal a perfect test (with 100% sensitivity; 100% specificity) while an area of 0.5 would equal a useless test (50% sensitivity; 50% specificity). (NCT00537056)
Timeframe: 12 weeks

InterventionParticipants (Count of Participants)
F-18 FDG PET/CT and DCE MRINA

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Adverse Events

Adverse events were monitored for on F-18 FDG PET/CT and DCE MRI imaging days: baseline (n=17); interim (n=12); and post-sunitinib therapy (n=17). Reported as the overall number of adverse events experienced. (NCT00537056)
Timeframe: up to 12 months

Interventionadverse events (Number)
F-18 FDG PET/CT and DCE MRI0

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Disease-free Survival (DFS)

Evaluate the value of pre-treatment FMISO results (T:B and HV) for all patients to predict the disease free survival outcome variables. (NCT00559377)
Timeframe: Up to 2 years

Interventionparticipants disease-free after 2 years (Number)
Disease-Free Survival10

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Overall Survival (OS)

Evaluate the value of pre-treatment FMISO results (T:B and HV) for all patients to predict the survival outcome variables. (NCT00559377)
Timeframe: For up to 2 years

Interventionparticipants still alive after 2 years (Number)
2 Year Overall Survival11

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Relationship Between Ki67 and Regional FMISO Uptake in Tumor

The value of the biomarker Ki67 analyses relates primarily to validating the information content of FMISO images. (NCT00559377)
Timeframe: Up to 2 years

Interventionpercentage of staining (Mean)
Patients With IHC Measures74

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Overall Response Rate (Patients That Achieve a CR or PR)

Assessed by Response Evaluation Criteria in Solid Tumors (RECIST) criteria. Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) for target lesions and assessed by MRI: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR. (NCT00564733)
Timeframe: At the end of 4 cycles of treatment, up to 24 weeks.

Interventionparticipants (Number)
Chemotherapy13

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Sensitivity and Specificity of FDG PET/CT and Tc99mHIDA in the Evaluation of Subjects Suspected of Cholecystitis

"Percent of patients identified of having cholecystitis using FDG PET/CT compared to patients identified of having pathological diagnosis of cholecystitis (sensitivity) Percent of patients identified of not having cholecystitis using FDG PET/CT compared to patients identified of not having pathological diagnosis of cholecystitis (specificity)~number of false positives = number of patients incorrectly identified of having cholecystitis using FDG PET/CT compared to a negative pathological diagnosis.~number of false negatives = number of patients incorrectly identified of not having cholecystitis using FDG PET/CT compared to a positive pathological diagnosis.~number of true positives = number of patients correctly identified of having cholecystitis using FDG PET/CT compared to a positive pathological diagnosis.~number of true negatives = number of patients correctly identified of not having cholecystitis using FDG PET/CT compared to a negative pathological diagnosis." (NCT00590395)
Timeframe: 1-2 days through the post operative period

InterventionParticipants (Count of Participants)
+PET/CT72094445-PET/CT72094445
+Path-PathN/A Path
Suspected Acute Cholecystitis9
Suspected Acute Cholecystitis0
Suspected Acute Cholecystitis1
Suspected Acute Cholecystitis2
Suspected Acute Cholecystitis6

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Number of Participants With Clinical Benefit

"FES SUV prior to endocrine treatment (dichotomized and as a continuous predictor) will also be tested as predictor of clinical benefit.~Patients were expected to start endocrine therapy within 2 weeks of the FES PET scan. Response assessment was evaluated at 3 and 6 months.~The initial (baseline) FES uptake was compared to clinical benefit (PD versus other outcome at 6 months)." (NCT00602043)
Timeframe: Up to 6 months

InterventionParticipants (Count of Participants)
Diagnostic FES: Average FES SUVmean >1.5, no Negative Sites8
Diagnostic FES: Patients With FES Negative Sites of Disease0

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Time to Progression

FES SUV prior to endocrine treatment (dichotomized and as a continuous predictor) will also be tested as predictor of time to progression. Analysis will be conducted using (respectively) logistic regression and Cox proportional hazards regression. This will include univariate analysis of FES and other predictive measures (ER/PgR expression, serum sex steroid levels), followed by an exploratory multivariate analysis combining FES SUV with other measures showing predictive capability univariate analysis. (NCT00602043)
Timeframe: Up to 6 months

Interventionmonths (Median)
Diagnostic (FES): Average FES SUVmean >1.5, no Negative Sites4.9
Diagnostic FES: Patients With FES Negative Sites of Disease2.2

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Best Overall Response

"Patients were expected to start endocrine therapy within 2 weeks of the FES PET scan. Response assessment was evaluated at 3 and 6 months. For patients with at least one site of measurable disease [per response evaluation criteria in solid tumors (RECIST, version 1.1)], size-based response criteria were used to assess response.~For patients without disease evaluable by RECIST 1.1, largely patients with bone-dominant metastatic breast cancer, serial FDG PET scanning was used to determine response. A decline in the FDG PET SUV (standard uptake value) of 30% or more was considered as response and an increase of 20% or more was considered to be progressive disease (PD).~The initial (baseline) FES uptake was compared to clinical benefit (PD versus other outcome at 6 months)." (NCT00602043)
Timeframe: Up to 6 months

Interventionpatients with progressive disease (Number)
Diagnostic FES: Average FES SUVmean >1.5, no Negative Sites5
Diagnostic FES: Patients With FES Negative Sites of Disease2

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To Determine the Biologic Effect of IV VEGF Trap on FDG Avidity After Four Cycles (Approximately 8 Weeks) of Therapy Through Pre- and Post-treatment FDG-PET Scans in Patients With Recurrent and/or Metastatic D-TC-FCO.

To determine the biologic effect of IV VEGF Trap on FDG avidity after four cycles (approximately 8 weeks) of therapy through pre- and post-treatment FDG-PET scans in patients with recurrent and/or metastatic D-TC-FCO. (NCT00729157)
Timeframe: 8 weeks

Interventionpercent of SUVm change (Median)
Treatment (Ziv-aflibercept and Fludeoxyglucose F 18).64

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The Safety and Toxicity Profile of IV VEGF Trap in Patients With Recurrent and/or Metastatic TC-FCO

The number of participants, with recurrent and/or metastatic TC-FCO, who experienced adverse events. Please see the adverse event table for the specifics for this protocol. (NCT00729157)
Timeframe: From the beginning of treatment through 30 days until participant comes off study

Interventionparticipants (Number)
Treatment (Ziv-aflibercept and Fludeoxyglucose F 18)36

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Effect of Thyroglobulin Concentration on Progression-free Survival

The change is serum thyroglobulin was measured by the percent change between the baseline value and the lowest value obtained while on treatment. (NCT00729157)
Timeframe: 6 months

Interventionpercent change serum thyroglobulin (Median)
Treatment (Ziv-aflibercept and Fludeoxyglucose F 18)0.4

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Progression-free Survival to Determine the 6-month Progression-free-survival (PFS) Rate

Progression-free survival to determine the 6-month progression-free-survival (PFS) rate (NCT00729157)
Timeframe: 6 months

Interventionmonths (Median)
Treatment (Ziv-aflibercept and Fludeoxyglucose F 18)5.4

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Radiographic Response Rate of Aflibercept in Patients With Recurrent and/or Metastatic Thyroid Cancer That Did Not Respond to Radioactive Iodine Therapy

Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) for target lesions & assessed by MRI: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + P RMeasurable lesions are defined as those that can be accurately measured in at least one dimension (longest diameter to be recorded) as ≥ 20 mm with conventional techniques (CT, MRI, x-ray) or as ≥ 10 mm with spiral CT scan. All tumor measurements must be recorded in millimeters (or decimal fractions of centimeters). All other lesions (or sites of disease), including small lesions (longest diameter < 20 mm with conventional techniques or < 10 mm using spiral CT scan), are considered non-measurable disease. Bone lesions, leptomeningeal disease, ascites, pleural/pericardial effusions, lymphangitis cutis/pulmonis, inflammatory breast disease, abdominal masses (not followed by CT or MRI), & cystic (NCT00729157)
Timeframe: After 8 weeks of study therapy

Interventionparticipants (Number)
Progression of DiseaseStable Disease
Treatment (Ziv-aflibercept and Fludeoxyglucose F 18)733

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Six Month Survival

The proportion of successes will be estimated by the number of surviving participants at 6 months divided by the total number of evaluable patients. A confidence interval for the 6-month survival rate was calculated using the exact binomial method. (NCT00735917)
Timeframe: Up to 6 months

Interventionpercentage of patients (Number)
Treatment (Saracatinib)11

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Overall Survival

Overall survival time is defined as the time from registration to death due to any cause. The median survival time and 95% confidence intervals will be estimated using the method of Kaplan-Meier. (NCT00735917)
Timeframe: Up to 2 years

Interventionmonths (Median)
Treatment (Saracatinib)2.5

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Progression-Free Survival

Time from the date of registration to the date of progression or death, whichever occurs first. Estimated by the method of Kaplan-Meier. (NCT00735917)
Timeframe: Progression and survival status assessed every month, up to 2 years

Interventionmonths (Median)
Treatment (Saracatinib)1.6

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Confirmed Tumor Responses (Complete Response [CR] or Partial Response [PR])

"A confirmed tumor response is defined to be a CR or PR noted as> the objective status on 2 consecutive evaluations at least 4 weeks apart. Response will be evaluated in this study using the new international criteria proposed by the revised Response Evaluation Criteria in Solid Tumors (RECIST) guideline (version 1.1)> > Complete Response (CR): Disappearance of all non-nodal target lesions and each target lymph node must have a reduction in short axis to <1.0 centimeters.>~> Partial response (PR): At least a 30% decrease in the sum of the longest diameters of the non-nodal target lesions and the short axes of the target lymph nodes taking as reference the baseline sum of diameters." (NCT00735917)
Timeframe: Evaluated using the first 6 courses of treatment

Interventionparticipants (Number)
Treatment (Saracatinib)0

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Time to Progression

The time to progression (defined as time in months from 3'-deoxy-3'-[18F] fluorothymidine (FLT)-scan until patient progressed) was compared between the two groups (patients with higher Maximum Standard Uptake Value (SUVmax) vs lower SUVmax, using the median SUV value). (NCT00775268)
Timeframe: up to 4.5 years

InterventionMonths (Mean)
Participants Scanned After Chemotherapy18.29

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18F- Fluorothymidine (FLT) Uptake Within the Tumor(s) Between Baseline vs Completion of Therapy Scans

FLT uptake within the tumor(s) using standard uptake value (SUVmax) was compared between baseline and completion of therapy scans. (NCT00775268)
Timeframe: up to 4.5 years

InterventionSUVmax (Mean)
BaselineCompletion of therapy scans
Participants Scanned at Baseline & After Chemotherapy9.150.9

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18F- Fluorothymidine (FLT) Uptake, Positron-emission Tomography (PET) Standard Uptake Value (SUV)Max in Malignant Residual Tumors Versus Benign Lesions After Therapy

FLT uptake was calculated within malignant residual tumors versus benign lesions using maximum standard uptake value (SUVmax). (NCT00775268)
Timeframe: up to 4.5 years

InterventionSUVmax (Mean)
Malignant LesionsBenign Lesions
Participants Scanned in the Evaluation of Residual Masses After Therapy5.51.7

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18F-fluorodeoxyglucose (18FDG) Standardized Uptake Values (SUV) Estimated Maximum and Tumor: Blood Pool Ratio at 1-hour Post-injection

After 1 hour post-injection of fluorodeoxyglucose (FDG), the maximum uptake value (SUVmax) (defined as radiotracer uptake in a region of interest normalized by the injected activity and body weight) was calculated was calculated within the residual mass. The ratio between SUVmax within the residual mass and SUVmean in the pool blood was measured. (NCT00775268)
Timeframe: up to 3.5 years

InterventionSUVmax/Tumor blood ratio (Number)
Patient 1Patient 2Patient 3Patient 4Patient 5Patient 6Patient 7Patient 8Patient 9Patient 10Patient 11Patient 12Patient 13Patient 14Patient 15Patient 16Patient 17Patient 18Patient 19Patient 20Patient 21
Participants Scanned in the Evaluation of Residual Masses After Therapy4.68.410.13.86.96.75.44.74.610.34.83.84.06.96.415.811.22.13.83.59.1

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3'-Deoxy-3'-[18F]-Fluorothymidine (FLT) Dynamic Influx Parameter (Ki) Standardized Uptake Values (SUV) Estimated Maximum at 1- and 2-hours Post-injection

The maximum uptake value (SUVmax) (defined as radiotracer uptake in a region of interest normalized by the injected activity and body weight) was calculated within the residual mass at 1 h and at 2 hours post-injection of FLT. (NCT00775268)
Timeframe: up to 3.5 years

,
InterventionSUV (Mean)
Patient 1Patient 2Patient 3Patient 4Patient 5Patient 6Patient 7Patient 8Patient 9Patient 10Patient 11Patient 12Patient 13Patient 14Patient 15Patient 16Patient 17Patient 18Patient 19Patient 20Patient 21Overall participants
Participants Scanned in the Evaluation of Residual Masses After Therapy at 1 Hour Post Injection0.72.08.91.61.37.53.41.66.52.32.52.27.64.51.93.94.77.91.11.56.43.6
Participants Scanned in the Evaluation of Residual Masses After Therapy at 2 Hours Post InjectionNA1.8NA0.87.94.63.21.26.02.02.41.57.44.21.63.64.57.91.1NA5.42.9

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Tumor Uptake With Fluorothymidine (FLT) - Maximum Standard Uptake Value (SUVmax)

The maximum standard uptake value (SUVmax) (defined as radiotracer uptake in a region of interest normalized by the injected activity and body weight) was measured within the tumor(s). The SUVmax was defined as the uptake value of the hottest pixels, within a volume of interest containing the entire tumor(s). (NCT00775268)
Timeframe: Up to 4.5 years

,
InterventionSUV (Mean)
Patient 1Patient 2Patient 3Patient 4Patient 5Patient 6Group-level (at baseline and after completion of therapy)
Participants Scanned After Completion of Therapy0.91.01.30.90.60.90.9
Participants Scanned at Baseline10.94.810.39.19.39.29.2

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Tumor(s) Maximum Standard Uptake Value (SUVmax) at Baseline and at Mid-treatment (Post-2 Cycles) Scan

The SUVmax (defined as radiotracer uptake in a region of interest normalized by the injected activity and body weight) was measured within the tumor(s). The SUVmax was defined as the uptake value of the hottest pixels, within a volume of interest containing the entire tumor(s). SUVmax was calculated at baseline and after 2-cycles of therapy. (NCT00775268)
Timeframe: Up to 4.5 years

InterventionSUVmax (Mean)
Baseline2-cycles post treatment
Participants Scanned at Baseline, at 2 Cycles & After ChemotherapyChemotherapy9.151.5

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Tumor(s) Maximum Standard Uptake Value (SUVmax) at Baseline Scan and SUVmax After Completion Scan in Responders and Non-responders' Patients

The SUVmax (defined as radiotracer uptake in a region of interest normalized by the injected activity and body weight) was measured within the tumor(s). The SUVmax was defined as the uptake value of the hottest pixels, within a volume of interest containing the entire tumor(s). SUVmax was calculated at baseline and after completion of therapy. (NCT00775268)
Timeframe: up to 4.5 years

InterventionStandard Uptake Value (SUV) - units (Median)
BaselineAfter completion of scan
Participants Scanned at Baseline & After Chemotherapy9.11.5

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Number of Participants With the Presence/Absence of Abnormal 18F- Fluorothymidine (FLT) Uptake, and Positive/Negative Biopsy

A positive malignant residual mass was defined as focal 18F- Fluorothymidine (FLT) uptake within the residual mass greater than the normal mediastinal background uptake. FLT uptake within the mass lower than the mediastinal was considered non-malignant. The positive/negative FLT uptake was correlated with biopsy results within the residual mass (presence or absence of malignant tumor cells). (NCT00775268)
Timeframe: Up to 3.5 years

InterventionParticipants (Count of Participants)
Presence of FLT uptakeAbsence of FLT uptake and FLT uptake lower than normal mediastinumPositive BiopsyNegative BiopsyBiopsy not performed
Participants Scanned in the Evaluation of Residual Masses After Therapy9127410

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Number of Participants With Non-serious Adverse Events Assessed by the Common Terminology Criteria for Adverse Events (CTCAE v4.0)

Here is the number of participants with non-serious adverse events assessed by the Common Terminology Criteria for Adverse Events (CTCAE v4.0). A non-serious adverse event is any untoward medical occurrence. A serious adverse event is an adverse event or suspected adverse reaction that results in death, a life-threatening adverse drug experience, hospitalization, disruption of the ability to conduct normal life functions, congenital anomaly/birth defect or important medical events that jeopardize the patient or subject and may require medical or surgical intervention to prevent one of the previous outcomes mentioned. (NCT00775268)
Timeframe: Date treatment consent signed to date off study, approximately 4 years, 7 months and 9 days.

InterventionParticipants (Count of Participants)
Participants Scanned at Baseline & After Chemotherapy7
Participants Scanned in the Evaluation of Residual Masses After Therapy20

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Primary Tumor Recurrence

To determine if higher 64Cu ATSM uptake is associated with earlier primary cervical tumor recurrence images were taken every 3 months for first 2 years and every 6 months during year 3, up to 3 years and evaluated for primary cervical tumor recurrence (NCT00794339)
Timeframe: every 3 months for first 2 years and every 6 months during year 3, up to 3 years

Interventiondays (Median)
T/M Below Median773.5
T/M at or Above Median797.0

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Relationship of Copper Cu 64-ATSM Uptake T/M Ratio and CA-IX Composite Score as a Marker of Tumor Hypoxia

"The Ratio of Tissue to Muscle (T/M) agent uptake measured at baseline was used as a predictor of Hypoxia Tumor Hypoxia was assessed with CA-IX markers using the~Composite Score (range 0-6):~Computed by using the coded values of Percentage of Tumor Cells Staining Score (0-3) multiplied by the coded value of Staining Intensity Score (0-2)." (NCT00794339)
Timeframe: Baseline

Interventionratio (Mean)
Composite Score: 07.58
Composite Score: 15.82
Composite Score: 28.04
Composite Score: 36.50
Composite Score: 410.60
Composite Score: 68.20

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Relationship of Copper Cu 64-ATSM Uptake T/M Ratio and CA-IX Staining Intensity Score: as a Marker of Tumor Hypoxia

"The Ratio of Tissue to Muscle (T/M) agent uptake measured at baseline was used as a predictor of Hypoxia Tumor Hypoxia was assessed with CA-IX markers using the~Staining Intensity Score:~0=No staining; 1=Weak staining; and 2=Moderate to strong staining." (NCT00794339)
Timeframe: baseline

Interventionratio (Mean)
No Staining7.58
Weak Staining6.20
Moderate to Strong Staining9.40

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Relationship of Copper Cu 64-ATSM Uptake T/M Ratio and Glucose Transporter 1 (GLUT1) Composite Score as a Marker of Tumor Hypoxia

"The Ratio of Tissue to Muscle (T/M) agent uptake measured at baseline was used as a predictor of Hypoxia Tumor Hypoxia was assessed with Glucose transporter 1 (GLUT1) markers using the~Composite Score (range 0-6):~Computed by using the coded values of Percentage of Tumor Cells Staining Score (0-3) multiplied by the coded value of Staining Intensity Score (0-2)." (NCT00794339)
Timeframe: Baseline

Interventionratio (Mean)
Composite Score: 09.70
Composite Score: 16.55
Composite Score: 26.89
Composite Score: 35.40
Composite Score: 48.93
Composite Score: 67.58

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Relationship of Copper Cu 64-ATSM Uptake T/M Ratio and Glucose Transporter 1 (GLUT1) Percentage of Tumor Cells Staining Score as a Marker of Tumor Hypoxia

"The Ratio of Tissue to Muscle (T/M) agent uptake measured at baseline was used as a predictor of Hypoxia Tumor Hypoxia was assessed with Glucose transporter 1 (GLUT1) markers using the~Percentage of Tumor Cells Staining Score:~0=<1% tumor cells; 1=1 33% tumor cells; 2=34 66% tumor cells; and 3=>66% tumor cells." (NCT00794339)
Timeframe: baseline

Interventionratio (Mean)
0=<1% Tumor Cells9.70
1-33% Tumor Cells6.01
34-66% Tumor Cells8.83
>66% Tumor Cells7.46

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Relationship of Copper Cu 64-ATSM Uptake T/M Ratio and Glucose Transporter 1 (GLUT1) Staining Intensity Score: as a Marker of Tumor Hypoxia

"The Ratio of Tissue to Muscle (T/M) agent uptake measured at baseline was used as a predictor of Hypoxia Tumor Hypoxia was assessed with GLUT-1 markers using the~Staining Intensity Score:~0=No staining; 1=Weak staining; and 2=Moderate to strong staining." (NCT00794339)
Timeframe: baseline

Interventionratio (Mean)
No Staining9.70
Weak Staining7.15
Moderate to Strong Staining8.11

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Relationship of Copper Cu 64-ATSM Uptake T/M Ratio and Vascular Endothelial Growth Factor (VEGF) Composite Score as a Marker of Tumor Hypoxia

"The Ratio of Tissue to Muscle (T/M) agent uptake measured at baseline was used as a predictor of Hypoxia Tumor Hypoxia was assessed with Vascular endothelial growth factor (VEGF) markers using the~Composite Score (range 0-6):~Computed by using the coded values of Percentage of Tumor Cells Staining Score (0-3) multiplied by the coded value of Staining Intensity Score (0-2)." (NCT00794339)
Timeframe: Baseline

Interventionratio (Mean)
Composite Score: 06.98
Composite Score: 14.44
Composite Score: 28.79
Composite Score: 36.59
Composite Score: 48.48
Composite Score: 611.76

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Relationship of Copper Cu 64-ATSM Uptake T/M Ratio and Vascular Endothelial Growth Factor (VEGF) Staining Intensity Score: as a Marker of Tumor Hypoxia

"The Ratio of Tissue to Muscle (T/M) agent uptake measured at baseline was used as a predictor of Hypoxia Tumor Hypoxia was assessed with Vascular endothelial growth factor (VEGF) markers using the~Staining Intensity Score:~0=No staining; 1=Weak staining; and 2=Moderate to strong staining." (NCT00794339)
Timeframe: baseline

Interventionratio (Mean)
No Staining6.98
Weak Staining7.50
Moderate to Strong Staining10.22

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Relationship of Copper Cu 64-ATSM Uptake T/M Ratio and VEGF Percentage of Tumor Cells Staining Score as a Marker of Tumor Hypoxia

"The Ratio of Tissue to Muscle (T/M) agent uptake measured at baseline was used as a predictor of Hypoxia Tumor Hypoxia was assessed with VEGF markers using the~Percentage of Tumor Cells Staining Score:~0=<1% tumor cells; 1=1 33% tumor cells; 2=34 66% tumor cells; and 3=>66% tumor cells." (NCT00794339)
Timeframe: baseline

Interventionratio (Mean)
0=<1% Tumor Cells6.98
1-33% Tumor Cells7.57
34-66% Tumor Cells8.51
>66% Tumor Cells8.44

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Relationship Between Copper Cu 64-ATSM Uptake in the Primary Tumor and Progression-free Survival 3 Years After Chemoradiotherapy

"Progression-free survival (PFS) evaluated every 3 months for first 2 years and every 6 months during year 3 to determine PFS at 3years.~Cu64-ATSM Uptake measured within 14 days of baseline Uptake is a measure of activity within a tumor~the maximum standardized uptake value (SUVmax = tracer uptake in ROI / (injected activity / patient weight))~Tumor-to-Muscle uptake ratio (T/M, An FDG-PET/CT-guided circular region of interest of 1.0-1.5 cm in diameter is drawn around the most intense region of the primary tumor to calculate the maximum uptake within the region. In addition, regions of interest are drawn on bilateral gluteal muscle groups on at least 3 slices, and the mean uptake is calculated. The T/M is the ratio of these measurements.)" (NCT00794339)
Timeframe: every 3 months for first 2 years and every 6 months during year 3, up to 3 years

,
Interventionratio (Mean)
Progression within 3 yearsNo progression within 3 years
64 CU-ATSM SUVmax @ Baseline4.44.2
64 CU-ATSM T/M Ratio @ Baseline8.28.0

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Lymph Node Metastasis at Baseline

"Lymph nodes were evaluated at 5 locations: Pelvic, Common Iliac, Para Aortic, Mediastinal, and Supraclavicular~This outcome looks at the Association of Ratio of Tissue to Muscle (T/M) uptake with Lymph Node Metastases at Baseline" (NCT00794339)
Timeframe: Two weeks

InterventionParticipants (Count of Participants)
Pelvic72187132Common Iliac72187132Para Aortic72187132Mediastinal72187132Supraclavicular72187132
Positive NodesNegative Nodes
Eligible Participants31
Eligible Participants27
Eligible Participants14
Eligible Participants41
Eligible Participants7
Eligible Participants48
Eligible Participants0
Eligible Participants55

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Copper Cu 64-ATSM T/M Uptake and Overall Survival

"To determine if higher 64Cu-ATSM uptake on PET/CT is associated with lower Overall survival (OS) T/M Uptake measured within 14 days of baseline;~Overall survival (OS) is measured every 3 months for first 2 years and every 6 months during year 3,until time of death or 3 years from baseline." (NCT00794339)
Timeframe: every 3 months for first 2 years and every 6 months during year 3, up to 3 years

Interventiondays (Median)
T/M Below Median773.5
T/M at or Above Median786.0

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Relationship Between Copper Cu 64-ATSM Uptake and Development of Distant Metastasis

Existence of distant metastasis was evaluated every 3 months for first 2 years and every 6 months during year 3 Copper Cu 64-ATSM Uptake (T/M) measured within 14 days of baseline; (NCT00794339)
Timeframe: every 3 months for first 2 years and every 6 months during year 3, up to 3 years

Interventiondays (Median)
T/M Below Median725.5
T/M at or Above Median786.0

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Relationship of Copper Cu 64-ATSM Uptake T/M Ratio and Carbonic Anhydrase IX (CA-IX) Percentage of Tumor Cells Staining Score as a Marker of Tumor Hypoxia

"The Ratio of Tissue to Muscle (T/M) agent uptake measured at baseline was used as a predictor of Hypoxia Tumor Hypoxia was assessed with Carbonic anhydrase IX (CA-IX) markers using the~Percentage of Tumor Cells Staining Score:~0=<1% tumor cells; 1=1 33% tumor cells; 2=34 66% tumor cells; and 3=>66% tumor cells." (NCT00794339)
Timeframe: baseline

Interventionratio (Mean)
0=<1% Tumor Cells7.58
1-33% Tumor Cells7.57
34-66% Tumor Cells9.40
>66% Tumor Cells7.35

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Participants Who Did Not Experience a Dose Limiting Toxicity in the Less Than 3 Centimeter Cohort

Number of Participants Who Did Not Experience a Dose Limiting Toxicity in the less than 3 centimeter cohort (NCT00852644)
Timeframe: 6 weeks

InterventionParticipants (Count of Participants)
56 Gray (LESS Than 3 Centimeter Cohort)3
62 Gray (LESS Less Than 3 Centimeter Cohort)3
68 Gray (LESS Than 3 Centimeter Cohort)0

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Participants Who Did Not Experience a Dose Limiting Toxicity in the More Than 3 Centimeter Cohort

The number of participants that did not experience a dose-limiting toxicity in the greater than 3 centimeter cohort (NCT00852644)
Timeframe: 6 weeks

InterventionParticipants (Count of Participants)
56 Gray (MORE Than 3 Centimeter Cohort)3
62 Gray (MORE Than 3 Centimeter Cohort)0
68 Gray (MORE Than 3 Centimeter Cohort)0

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Feasibility of Ultra Short-term Steroid Therapy to Increase the Accuracy of FDG-PET/CT Imaging

The blood glucose of all patients will be checked by accu-check before the injection of 18F-FDG. The acceptable blood glucose level will be ≤120 mg/dl. Any participant experienced elevated fasting blood glucose of more than 120 mg/dl after steroid therapy, he /she will be asked to come back to the PET center within 48 hours to check the blood glucose level. If the blood glucose level did not decline to baseline level, the participant will be asked to follow with his/her family doctor for management. Participants with history of systemic hypertension will be monitored for increased blood pressure. After 50-to-70 minutes period for FDG incorporation into presumed lesions, patient will under go a limited 18F-FDG PET/CT for the area of the interest (1-2 bed positions). PET imaging will be performed using a GE Discovery STE PET/CT system (GE Medical Systems, Milwaukee, WI). (NCT00906503)
Timeframe: 24-48 hours

Interventiongm/ml (Mean)
Malignant nodulesBenign nodules
PET/Computed Tomography (CT)3.974.27

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Progression Free Survival by Smoking Status

Percent of patients that were progression free by smoking status (NCT00941070)
Timeframe: at 18 months from study entry

Interventionpercentage of paticipants (Number)
Non-SmokersSmokers that quit while on studySmokers
Treatment (Cisplatin, Triapine, Radiation Therapy)768950

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Progression Free Survival by HPV Subtype

Tabular descriptive data will be presented. HPV sub-type will be associated with treatment related toxicity, clinical response, PET metabolic response, and overall clinical outcome. Kaplan-Meier (product-limit) method of survival estimation will be used. Tests of equivalence of the estimates will be compared using the Wilcoxon long-rank test using a threshold for statistical significance of P 0.05. Cox proportional hazards regression models will be used in multivariate analyses. (NCT00941070)
Timeframe: Baseline

Interventionpercentage of patients (Number)
HPV16/18HPV-naive tumors
Treatment (Cisplatin, Triapine, Radiation Therapy)7483

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Clinical and Objective Response Assignment

Number of patients with a complete clinical responses defined as disappearance of all target lesions. A complete metabolic response on PET/CT will be defined as absence of abnormal FDG uptake at sites of abnormal FDG uptake noted on pre-treatment FDG-PET study. (NCT00941070)
Timeframe: one month follow up assessment

Interventionparticipants (Number)
Treatment (Cisplatin, Triapine, Radiation Therapy)23

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Clinical and Objective Response Assignment

Number of patients with a complete clinical responses defined as disappearance of all target lesions. A complete metabolic response on PET/CT will be defined as absence of abnormal FDG uptake at sites of abnormal FDG uptake noted on pre-treatment FDG-PET study. (NCT00941070)
Timeframe: post therapy at 3 months

Interventionparticipants (Number)
Treatment (Cisplatin, Triapine, Radiation Therapy)21

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Clinical and Objective Response Assignment

Number of patients with a complete clinical responses defined as disappearance of all target lesions. A complete metabolic response on PET/CT will be defined as absence of abnormal FDG uptake at sites of abnormal FDG uptake noted on pre-treatment FDG-PET study. (NCT00941070)
Timeframe: three month follow up assessment

Interventionparticipants (Number)
Treatment (Cisplatin, Triapine, Radiation Therapy)23

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Percent of Patients With Incidence of Grade 2 or Higher Gastrointestinal and Genitourinary Toxicity, Assessed Using CTCAE v3.0 Until December 31, 2010 and CTCAE v4.0 Beginning January 1, 2011

Information will include the type, severity, time of onset, time of resolution, and the probable association with the study regimen. Frequency tables will be constructed to summarize observed incidence by severity and type of toxicity. (NCT00941070)
Timeframe: After 5 weeks of radiation therapy

Interventionpercentage of patients (Number)
Treatment (Cisplatin, Triapine, Radiation Therapy)0

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PET/CT Scan Metabolic Activity

Descriptive tabular data reporting mean, standard deviation, minimum, maximum provided by metabolic response cohort. Status of 3-month post-treatment metabolic response associated with clinical response measured by RECIST criteria and with overall clinical outcome. Kaplan-Meier (product-limit) method of survival estimation used. Tests of equivalence of the estimates compared using the Wilcoxon long-rank test using P 0.05. Cox proportional hazards regression models used in multivariate analyses. (NCT00941070)
Timeframe: 3 months post-treatment

InterventionStandard Uptake Value (SUV) (Median)
Treatment (Cisplatin, Triapine, Radiation Therapy)2.6

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Change in Smoking Behavior, Assessed Using the Smoking Questionnaire and Cessation Counseling

(NCT00941070)
Timeframe: 18 months from study entry

Interventionparticipants (Number)
Non-SmokersSmokers that quit while on studyCurrent smokers
Treatment (Cisplatin, Triapine, Radiation Therapy)9115

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Progression-free Survival

Percentage of patients that did not have disease progression. Estimates of progression-free survival will be computed using the product-limit estimate of Kaplan and Meier. (NCT00941070)
Timeframe: at 18 months from study entry

Interventionpercentage of patients (Number)
Treatment (Cisplatin, Triapine, Radiation Therapy)67

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PET/CT Scan Metabolic Activity

Descriptive tabular data reporting mean, standard deviation, minimum, maximum provided by metabolic response cohort. Status of 3-month post-treatment metabolic response associated with clinical response measured by RECIST criteria and with overall clinical outcome. Kaplan-Meier (product-limit) method of survival estimation used. Tests of equivalence of the estimates compared using the Wilcoxon long-rank test using P 0.05. Cox proportional hazards regression models used in multivariate analyses. (NCT00941070)
Timeframe: Baseline (pre-therapy)

InterventionStandard Uptake Value (SUV) (Median)
Treatment (Cisplatin, Triapine, Radiation Therapy)14.6

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Fasting F-18 Fluorodeoxyglucose (FDG) Positron Emission Tomography (PET/CT) Imaging Complete Metabolic Response, Reported Following National Cancer Institute (NCI) and European Organization for Research and Treatment of Cancer (EORTC) Guidelines.

To quantitate change in pre-treatment standard uptake value (SUV) on PET/CT and posttreatment PET/CT or disease progression PET/CT. Change in PET/CT SUV will be associated with 3-month best overall clinical response. (NCT00941070)
Timeframe: post therapy at 3 months

InterventionStandard uptake value (SUV) (Median)
Pretherapy SUVPosttherapy SUV
Treatment (Cisplatin, Triapine, Radiation Therapy)14.62.6

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Change in FLT Uptake in Responders and Non-responders

Unadjusted analysis will be performed utilizing students t-tests. If the data appears non-normal, the Wilcox on rank-sum test will be used rather than the t-test. Adjusted analysis will be performed utilizing logistic regression. (NCT00963807)
Timeframe: Baseline and 6 weeks

InterventionSULmax (Mean)
Responders-1.8
Non-Responders1.2

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Overall Response Rate Reported as a Proportion of the Total Number of Patients Who Received at Least One Cycle of Therapy Assessed Using Response Evaluation Criteria in Solid Tumors (RECIST)

RECIST version 1.1 was utilized for this outcome measure. A detailed description of RECIST 1.1 can be found here: Nishino M, Jackman DM, Hatabu H, Yeap BY, Cioffredi LA, Yap JT, et al. New Response Evaluation Criteria in Solid Tumors (RECIST) guidelines for advanced non-small cell lung cancer: comparison with original RECIST and impact on assessment of tumor response to targeted therapy. AJR Am J Roentgenol 2010;195:W221-8. (NCT00963807)
Timeframe: Up to 6 weeks

Interventionpercentage of participants (Number)
Treatment (Docetaxel, Cisplatin, Dexamethasone, and Surgery)33

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Change in FLT Uptake

Will be calculated by subtracting the uptake of the scan after the second cycle of chemotherapy from the uptake of the pre-treatment scan. (NCT00963807)
Timeframe: Baseline and 6 weeks

InterventionSULmax (Mean)
Treatment (Docetaxel, Cisplatin, Dexamethasone, and Surgery)0.2

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Change in 18F-Fluorodeoxyglucose (FDG) Uptake

Will be calculated by subtracting the baseline FDG uptake from the post-cycle 2 uptake (as measured by SULmax). (NCT00963807)
Timeframe: Baseline and 6 weeks

InterventionSULmax (Mean)
Treatment (Docetaxel, Cisplatin, Dexamethasone, and Surgery)-3.8

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Change in 18F-Fluorothymidine (FLT) Uptake

Will be calculated by subtracting the uptake of the scan after the first cycle of chemotherapy from the uptake of the pre-treatment scan.. Change in FLT uptake will be measured using the maximum standard uptake value adjusted for lean body mass (SULmax), which is a measure of how much radiotracer (in this case FLT) is being consumed by cells. (NCT00963807)
Timeframe: Baseline and 3 weeks

InterventionSULmax (Mean)
Treatment (Docetaxel, Cisplatin, Dexamethasone, and Surgery)-0.4

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Number of Participants With Adverse Events

Here is the number of participants with adverse events (NCT00971789)
Timeframe: 47 months

InterventionParticipants (Number)
Sirolimus Patients17

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Percentage Change in Maximum Lesional FDG Uptake From 60 to 180 Minutes After FDG Administration

Lesional fluorodeoxyglucose (FDG) uptake is measured by standardized uptake value (SUV). The study compared the percentage of change in maximum SUV over 2 hours (first measure was 60 minutes post-administration and second timepoint was 180 minutes post-administration). (NCT01004718)
Timeframe: 2 hours (between 60 minutes post-administration and 180 minutes post-administration)

Interventionpercentage of change in maximum SUV (Mean)
Diffuse Large B-cell Lymphoma36.2
Hodgkin's Lymphoma32

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Changes in the Level of Specific T Lymphocytes

Mean percent change from baseline of T lymphocytes. (NCT01038778)
Timeframe: Baseline to approximately 4 weeks post-treatment, up to 1 year

Interventionpercentage of cells count (Mean)
Dose Level 126.3
Dose Level 210.5

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Incidence of Toxicities

The number of participants with serious adverse events. (NCT01038778)
Timeframe: Up to 30 days

InterventionParticipants (Count of Participants)
Treatment (Entinostat, Aldesleukin)9

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Dose-limiting Toxicities of Entinostat When Combined With Aldesleukin Within the Phase I

Number of dose-limiting toxicities of entinostat when combined with aldesleukin within the Phase I MEASUREMENT OF EFFECT Patients underwent CT scans at week 11 (+/- 7 days) of each cycle during aldesleukin administration and then every 8-12 weeks (+/- 2 weeks). Response Evaluation Criteria in Solid Tumors (RECIST V.1.0) (NCT01038778)
Timeframe: 84 days

InterventionParticipants (Count of Participants)
Dose Level 10
Dose Level 20

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Time-to-tumor Progression

The median time to tumor progression (TTP) was estimated using standard Kaplan-Meier methods, where estimates of the median were obtained with 95% confidence intervals (CIs). TTP was defined as the time from the start of treatment to progression or last follow-up. Patients that did not progress were censored. (NCT01038778)
Timeframe: up to 12-months after the last subject enrolls

Interventionmonths (Median)
Treatment (Entinostat, Aldesleukin)14

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Incidence of Toxicity (Phase I)

Count of participants with grade 4 toxicity. The frequency and grade of toxicities will be tabulated for each dose level. (NCT01038778)
Timeframe: 84 days

InterventionParticipants (Count of Participants)
Dose Level 11
Dose Level 20

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Overall Response Rate (Complete Plus Partial) (Phase II)

"The proportion of patients who have a partial or complete response to treatment evaluated by RECIST V.1.0 criteria.~MEASUREMENT OF EFFECT Patients underwent CT scans at week 11 (+/- 7 days) of each cycle during aldesleukin administration and then every 8-12 weeks (+/- 2 weeks). Response Evaluation Criteria in Solid Tumors (RECIST V.1.0)" (NCT01038778)
Timeframe: Up to 12 months

InterventionProportion of participants (Number)
Treatment (Entinostat, Aldesleukin).39

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Overall Survival

The 3-year overall survival (OS) rate was estimated using standard Kaplan-Meier methods, where estimates of the median were obtained with 95% confidence intervals (CIs). OS was defined as the time from the start of treatment to death due to any cause or last follow-up, patients who did not die were censored. (NCT01038778)
Timeframe: up to 12-months after the last subject enrolls

Interventionpercentage of participants (Number)
Treatment (Entinostat, Aldesleukin)82.1

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Progression-free Survival

"The median progression-free survival (PFS) was estimated using standard Kaplan-Meier methods, where estimates of the median were obtained with 95% confidence intervals (CIs). PFS was defined as the time from the start of treatment to progression or death due to any cause or last follow-up, patients who did not progress or die were censored.~MEASUREMENT OF EFFECT Patients underwent CT scans at week 11 (+/- 7 days) of each cycle during aldesleukin administration and then every 8-12 weeks (+/- 2 weeks). Response Evaluation Criteria in Solid Tumors (RECIST V.1.0)" (NCT01038778)
Timeframe: up to 12-months after the last subject enrolls

Interventionmonths (Median)
Treatment (Entinostat, Aldesleukin)14.0

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Overall Response

Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) for target lesions and assessed by MRI: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR (NCT01129206)
Timeframe: Approximately three years

Interventionpatients (Number)
Stable diseaseProgressive disease
Arm I: Pralatrexate and Docetaxel24

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Overall Survival (OS)

OS was determined from the date of start of therapy to death frm any cause. (NCT01129206)
Timeframe: Approximately five years

Interventionmonths (Median)
Arm I5.5

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Progression-free Survival (PFS)

Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions (NCT01129206)
Timeframe: Approximately three years

Interventionmonths (Median)
Arm I: Pralatrexate and Docetaxel1.9

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Correlation of FDG PET Response With Response Rate

Radiological assessment of tumor response was performed by computed tomography (CT) and positron emission tomography (PET) every four cycles of therapy and responses were measured according to RECIST and PERCIST criteria. (NCT01129206)
Timeframe: Approximately three years

,
Interventionpatients (Number)
Progressive DiseaseStable DiseasePartial Response
PERCIST Criteria Per PET022
RECIST Criteria Per CT420

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36 Month Progression Free Survival Rate of Patients Receiving 4 Cycles of ABVD Versus Patients Receiving 2 Cycles of ABVD and 2 Cycles of BEACOPP and Radiation.

All patients received an initial 2-28 day cycles of doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) on Days 1 and 15. After the first 2 cycles of ABVD, PET/CT was performed and submitted for central review (cycle 2, days 23-25) and determined whether patients would receive 2 cycles of escalated BEACOPP and involved-field RT (IFRT) or an additional 2 cycles of ABVD. PFS for each patient is measured as the time from registration on trial to the first incident of death or progression. The PFS rate at 36 months is calculated as the number of patients who have a progression-free survival time greater than 36 months divided by the total number of patients that started treatment. For this endpoint, we compare the PFS rate between patients who received 4 cycles of ABVD and patients who received 2 cycles of ABVD and 2 cycles of IFRT. (NCT01132807)
Timeframe: at 36 months

Interventionproportion of participants (Number)
Treatment (ABVD:4 Cycles).91
Escalated BEACOPP and Involved Field Radiation Therapy.67

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Complete Response Rate

A Complete Response (CR) was defined as having the following conditions: 1. A complete disappearance of all detectable clinical evidence of disease and disease-related symptoms if present before therapy. 2. In patients with a PET scan that was positive before therapy, a post-treatment residual mass of any size is permitted as long as it is PET-negative. A Complete Response rate was defined as the number of patients who achieved a CR divided by the number of patients that were eligible for analysis in each group. The CR rate was calculated for patients that completed 4 cycles of ABVD and for patients that completed 2 cycles of ABVD and 2 cycles of BEACOPP and IFRT. (NCT01132807)
Timeframe: Up to 5 years

Interventionproportion of participants (Number)
Treatment (ABVD: 4 Cycles).97
Escalated BEACOPP and Involved Field Radiation Therapy.85

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Progression-Free Survival (PFS) at 36-Months for Patients Who Received 4 Cycles of ABVD

The primary objective of this trial is to estimate the 3 year PFS in patients who received 4 cycles of ABVD. PFS for each patient is measured as the time from registration on trial to the first incident of death or progression. The PFS at 36 months is calculated as the number of patients who have a progression-free survival time greater than 36 months divided by the total number of patients that started treatment. For this endpoint, all patients that received 4 cycles of doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD) are included. (NCT01132807)
Timeframe: 36 Months

Interventionproportion of patients (Number)
Treatment (ABVD: 4 Cycles).91

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Evaluate Acute Gastrointestinal Toxicity up to 3 Months of Treatment.

Acute grade 2 or greater gastritis, fistula, enteritis, or ulcer or any other grade 3-4 gastrointestinal toxicity within 3 months of treatment. (NCT01146054)
Timeframe: Within 3 months of treatment.

InterventionNumber of toxicities. (Number)
SBRT and Gemzar14

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To Evaluate Progression Free Survival Following Gemcitabine and SBRT for up to 5 Years of Follow up .

"Time to progression free survival is measured from start of SBRT treatment until first progression event or death, which ever comes first. If the patient did not have an event, then the patient was censored at the last follow up.~The analysis was a Kaplan-Meier curve and the outcome was the median time to progression free survival." (NCT01146054)
Timeframe: Up to 5 years of follow up.

InterventionMonths (Median)
SBRT and Gemzar7.8

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To Determine the Rate of (Grade 2 or Greater) Gastrointestinal Toxicity Attributable to Gemcitabine and Fractionated SBRT at One Year.

Grade 2 or greater late gastritis, fistula, enteritis, or ulcer or late grade 3-4 gastrointestinal toxicity at one year. (NCT01146054)
Timeframe: One year.

InterventionNumber of toxicities. (Number)
SBRT and Gemzar5

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To Determine the Overall Survival in Pancreatic Cancer Patients Treated With Gemcitabine and SBRT for up to 5 Years of Follow up.

Time to death was measured from start of treatment to until death. If death was not observed, the patient was censored at last follow up. (NCT01146054)
Timeframe: Up to 5 years of follow up.

InterventionMonths (Median)
SBRT and Gemzar13.9

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Proportion of Participants Achieving Freedom From Local Progression (FFLP) in Patients Treated With Gemcitabine Followed by Fractionated Stereotactic Body Radiotherapy (SBRT) for up to 5 Years of Follow up.

"Freedom from local progression is defined as the time from start of SBRT treatment to local progression, with death as a competing risk. If the patient neither died nor experienced local progression, then patient was censored at last follow up.~The data was analyzed in a competing risk model and the outcome reported was the 1 year cumulative incidence rate." (NCT01146054)
Timeframe: Up to 5 years of follow up.

InterventionProportion of participants with FFLP (Number)
SBRT and Gemzar0.78

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Changes From Baseline Hypoxic Volume (HV)

ANOVA and Kruskal-Wallis analysis will be performed across the different categories to look for significant associations. (NCT01169350)
Timeframe: Baseline and up to 2 years

InterventionCm^3 (Mean)
Diagnostic (18F FDG and 18F FMISO PET/CT)9.7

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Comparison of Serum Angiogenic Marker Reverse Contrast Transfer Rate (Kep) Between MGUS and SMM/MM Groups

Pharmacokinetic parameter Kep was measured by dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI). (NCT01237054)
Timeframe: 60 days

Interventionper min (Mean)
MGUS (Monoclonal Gammopathy of Undetermined Significance)4.05
SMM (Smoldering Multiple Myeloma)/MM (Multiple Myeloma)6.93

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Comparison of Serum Angiogenic Markers Ang2 (Angiopoietin), G-CSF (Granulocyte-colony Stimulating Factor), Follistatin, HGF (Hepatocyte Growth Factor), FGF-1, Endothelin 1, and VEGF-A (Vascular Endothelial Growth Factor-A) Between MGUS and SMM/MM Groups

The assay was performed according to the manufacture's protocol, and all samples were diluted 1:3. Cytokine values were calculated using a five-parameter standard curve with Bio-Plex Manager 6.1. (NCT01237054)
Timeframe: 60 days

,
Interventionpg/ml (Mean)
Ang2 (angiopoietin)G-CSF (granulocyte-colony stimulating factor)FollistatinHGF (hepatocyte growth factor)VEGF-A (vascular endothelial growth factor-A)FGF-1 (fibroblast growth factor 1)Endothelin 1
MGUS (Monoclonal Gammopathy of Undetermined Significance)2465.9724.92562.45390.57844.31NANA
SMM (Smoldering Multiple Myeloma)/MM (Multiple Myeloma)3804.42101.08823.15654.341301.52NANA

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Count of Participants With Positive and Negative 18F-FDG PET CT and F18-NaF PET CT Imaging Results in Individuals With MGUS, SMM, and MM.

18F-FDG PET CT and F18-NaF PET CT imaging results were compared in participants with MGUS, SMM, and MM. Lesions were considered positive if focal uptake corresponded to lesions identified on CT for NaF and negative if no uptake seen in lesions. Criteria to define FDG positivity included parameters published by Zamagni et al with focal abnormal uptake more intense than background. (NCT01237054)
Timeframe: 60 days

,,
InterventionParticipants (Count of Participants)
Positive 18F-FDG PET CT resultNegative 18F-FDG PET CT resultPositive F18-NaF PET CT resultNegative F18-NaF PET CT result
MGUS (Monoclonal Gammopathy of Undetermined Significance)010010
MM (Multiple Myeloma)5591
SMM (Smoldering Multiple Myeloma)19010

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Count of Participants With Positive DCE-MRI Imaging Results

DCE-MRI, an FDA approved gadolinium chelate (e.g. Magnevist, Berlex Laboratories, NJ, USA) will be administered intravenously at 3 cc/sec using an automated pump injector (Medrad, Pittsburgh, PA, USA). The criteria was presence of early and diffuse hyper-enhancement compared to the surrounding bone marrow. The pattern of marrow involvement on MRI was characterized as: (1) normal when there was no evidence of abnormal signal intensity; (2) focal, which consisted of localized areas of abnormal marrow; the lesions are darker than yellow marrow and slightly darker than or isointense to red marrow on T1-weights images; (3) diffuse, in which normal bone marrow signal intensity is completely absent, the intervertebral disks appear brighter than or isointense to the diseased marrow; and finally (4) heterogeneous that consists of innumerable small foci of disease on a background of intact marrow, with small dark lesions on T1-weighted images, which become bright on T2-weighted image. (NCT01237054)
Timeframe: 60 days

,,
InterventionParticipants (Count of Participants)
PositiveNegativeMissingUnclear
MGUS (Monoclonal Gammopathy of Undetermined Significance)1900
MM (Multiple Myeloma)9010
SMM (Smoldering Multiple Myeloma)1900

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Comparison of Reverse Contrast Transfer Rate (Kep) and Forward Contrast Transfer Rate (Ktrans) Among Patients With MGUS, SMM, and MM

Pharmacokinetic parameters Kep and Ktrans were measured by dynamic contrast-enhanced magnetic resonance imaging (DCE-MRI). (NCT01237054)
Timeframe: 60 days

,,
Interventionper min (Median)
KepKtrans
MGUS (Monoclonal Gammopathy of Undetermined Significance)3.92.4
MM (Multiple Myeloma)5.83.1
SMM (Smoldering Multiple Myeloma)92.3

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Comparison of Microvessel Density (MVD) Among Patients With MGUS, SMM, and MM

Microvessel density was estimated by determining the average number of cluster of differentiation 34 (CD34)-stained microvessels in 10 areas of maximal MVD counted at a high-power field (h.p.f. x 500 magnification). Large vessels and vessels in the periosteum on bone were excluded. Areas of staining with no discrete breaks were counted as a single vessel. The presence of a lumen was not required. (NCT01237054)
Timeframe: 60 days

Interventionmicrovessels/hpf (Median)
MGUS (Monoclonal Gammopathy of Undetermined Significance)15
SMM (Smoldering Multiple Myeloma)19.4
MM (Multiple Myeloma)20.9

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Comparison of Microvessel Density (MVD) Between MGUS and SMM/MM Groups

Microvessel density was estimated by determining the average number of CD34-stained microvessels in 10 areas of maximal MVD counted at a high-power field (h.p.f. x 500 magnification). (NCT01237054)
Timeframe: 60 days

Interventionmicrovessels/hpf (Mean)
MGUS (Monoclonal Gammopathy of Undetermined Significance)15.04
SMM (Smoldering Multiple Myeloma)/MM (Multiple Myeloma)21.64

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Complete Response Rate

"A complete response was defined using International Harmonization Project Response Criteria as the complete disappearance of all detectable clinical evidence of disease and disease-related symptoms if present before therapy. If the bone marrow was involved by lymphoma before treatment, the infiltrate must have cleared on repeat bone marrow biopsy.~The complete response (CR) rate was calculated in newly diagnosed untreated follicular lymphoma patients receiving 6 cycles of ofatumumab-bendamustine (ARM A) and 6 cycles of ofatumumab, bortezomib, and bendamustine (ARM B).~The complete response rate was calculated as the number of patients with a complete response divided by the number of patients eligible for evaluation." (NCT01286272)
Timeframe: From date of randomization until patient stops treatment for any reason, up to 484 days post-randomization

Interventionproportion of patients (Number)
Arm A (Ofatumumab, Bendamustine Hydrochloride).621
Arm B (Ofatumumab, Bendamustine Hydrochloride, Bortezomib).597

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Progression-free Survival (PFS)

Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions. PFS rates (percentages) at 1, 2, ,3 and 4 years are defined as the percentage of patients who are alive and progression-free at the respective time points. The p-values of the log-rank test will be calculated to compare PFS between the two arms. (NCT01286272)
Timeframe: Up to 4 years

,
Interventionpercentage of patients (Number)
PFS at 1 yearPFS at 2 yearsPFS at 3 yearsPFS at 4 years
Arm A (Ofatumumab, Bendamustine Hydrochloride)93.880.365.957.3
Arm B (Ofatumumab, Bendamustine Hydrochloride, Bortezomib)84.875.667.164.7

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Five-year Progression-free Survival (PFS) Rate in Patients With Newly Diagnosed Limited Stage Diffuse Large B-cell Lymphoma (DLBCL)

"Measured from date of registration to date of first observation of progressive disease, or death due to any cause. Patients last known to be alive without report of progression or relapse are censored at date of last contact.~Progressions is defined using the 2007 revised Cheson et. Al. criteria, as ≥50% increase in the sum of the products of diameters (SPD) of target measurable lesions, appearance of any new bone marrow involvement, or appearance of any new lesion >1.5 cm in the longest axis." (NCT01359592)
Timeframe: up to 5 years

Interventionpercentage of participants (Number)
R-CHOP x 3 Followed by PET-directed Therapy87

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Progression-free Survival (PFS) Within the PET+ and PET- Subgroups of Patients With Newly Diagnosed Limited-stage Diffuse Large B-Cell Lymphoma (DLBCL)

Measured from date of interim positron emission tomography (PET)/computed tomography scan to date of first observation of progressive disease, or death due to any cause. Patients last known to be alive without report of progression or relapse are censored at date of last contact. (NCT01359592)
Timeframe: up to 5 years

Interventionpercentage of participants (Number)
Interim PET-negative89
Interim PET-positive86

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Overall Survival of Patients With Newly Diagnosed Limited-stage Diffuse Large B-Cell Lymphoma (DLBCL)

Measured from date of registration to date of death due to any cause. Patients last known to be alive are censored at date of last contact. (NCT01359592)
Timeframe: up to 5 years

Interventionpercentage of participants (Number)
R-CHOP x 3 Followed by PET-directed Therapy89

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Response Rate Defined as Partial Response (PR)

Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.1) for target lesions and assessed by MRI: Partial Response: At least a 30% decrease in the sum of diameters of target lesions, taking as reference the baseline sum diameters. Standard estimates of the binomial proportion will be used to estimate and place confidence bounds on the several response rates. (NCT01462630)
Timeframe: 3 months

InterventionParticipants (Count of Participants)
Treatment (Enzyme Inhibitor Therapy)1

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Evaluation of Toxicity of Pazopanib Hydrochloride in This Patient Population

Toxicities related/unrelated to study treatment with >10% frequency (NCT01462630)
Timeframe: Up to 2 years

Interventiontoxicities (Number)
Treatment (Enzyme Inhibitor Therapy)189

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Overall Survival of Patients Treated With Pazopanib Hydrochloride

Estimated using the method of Kaplan and Meier. (NCT01462630)
Timeframe: Up to 107 weeks

Interventionweeks (Median)
Treatment (Enzyme Inhibitor Therapy)69.8

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PFS Rate

Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.1), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions. PFS was estimated using the method of Kaplan and Meier. (NCT01462630)
Timeframe: 3 months

Interventionpercentage of patients (Number)
Treatment (Enzyme Inhibitor Therapy)54.6

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Response Rate Defined as CR

Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.1) for target lesions and assessed by MRI: Disappearance of all target lesions. Any pathological lymph nodes (whether target or non-target) must have reduction in short axis to <10 mm. Standard estimates of the binomial proportion will be used to estimate and place confidence bounds on the several response rates. (NCT01462630)
Timeframe: 3 months

InterventionParticipants (Count of Participants)
Treatment (Enzyme Inhibitor Therapy)0

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Response Rate According to RECIST

"A 90% score (Wilson) confidence interval will be computed for the response rate.~Clinical benefit according to Recist score is defined as: Stable Disease, Partial Remission or Complete Remission. Lack of clinical benefit is defined as Progressive Disease (increase in target lesion size by 20% or more)." (NCT01720602)
Timeframe: 8 weeks

Interventionpercentage of patients (Number)
Treatment (Vorinostat, AI Therapy)60

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Duration of Response

Duration of response will be summarized for responders. (NCT01720602)
Timeframe: Up to 5 years

Interventionweeks (Median)
Treatment (Vorinostat, AI Therapy)29.6

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Rate of Clinical Benefit of Patients Receiving Vorinostat/AI Combination Therapy According to RECIST

"A 90% score (Wilson) confidence interval will be computed for the rate of clinical benefit.~Clinical benefit according to Recist score is defined as: Stable Disease, Partial Remission or Complete Remission. Lack of clinical benefit is defined as Progressive Disease (increase in target lesion size by 20% or more)." (NCT01720602)
Timeframe: 8 weeks

Interventionpercentage of patients (Number)
Treatment (Vorinostat, AI Therapy)60

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Progression-free Survival (PFS)

Progression-free survival is assessed relative to the start of the study therapy. Progression can be determined by RECIST 1.1, elevated tumor markers, worsening clinical symptoms or new lesions identified by FDG-PET or bone scan. (NCT01720602)
Timeframe: From the time of start of study therapy to documented progression - up to 5 years

Interventionmonths (Median)
Treatment (Vorinostat, AI Therapy)2

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Overall Survival

Overall survival is assessed relative to the start of the study therapy to the date of death, from any cause. (NCT01720602)
Timeframe: From the time of start of study therapy to date of documented death

Interventionmonths (Median)
Treatment (Vorinostat, AI Therapy)19

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Change From Baseline in Maximum Standard Uptake Values (SUVmax)

Maximum standard uptake values (SUVmax) were assessed on the basis of position emission tomography (PET) scans using radiotracers 18F-FPPRGD2 and 18F-FDG at baseline and at regular medical care follow-up (6 to 12 weeks after initiation of treatment). The outcome is assessed as the difference in the maximum standard uptake values (SUVmax) values from baseline to follow-up for the 2 radiotracers, and will be reported for each disease type as the median with standard deviation. (NCT01806675)
Timeframe: At baseline and 6 weeks

,
Interventionratio (Median)
18F-FPPRGD2 PET scans18F-FDG PET scans
Gynecological Cancers0.09-1.90
Renal Cell Cancer (RCC)0.107.8

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Change in Tumor Size

The treatment effect for participants with gynecological cancers (GYN) and renal cell carcinoma (RCC) was assessed on the basis of change in tumor size as determined by pre- and post-treatment CT scans. The outcome is reported as the difference at treatment follow-up, reported as the median with standard deviation. (NCT01806675)
Timeframe: 9 to 12 weeks

Interventioncentimeters (Median)
Gynecological Cancers0.9
Renal Cell Cancer (RCC)1

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Change From Baseline in Maximum Standard Uptake Values (SUVmax)

Maximum standard uptake values (SUVmax) were assessed on the basis of position emission tomography (PET) scans using radiotracers 18F-FPPRGD2 and 18F-FDG at baseline and at regular medical care follow-up (6 to 12 weeks after initiation of treatment). The outcome is assessed as the difference in the maximum standard uptake values (SUVmax) values from baseline to follow-up for the 2 radiotracers, and will be reported for each disease type as the median with standard deviation. (NCT01806675)
Timeframe: At baseline and 6 weeks

Interventionratio (Median)
18F-FPPRGD2 PET scans
Glioblastoma Multiforme (GBM)-0.98

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Tumor Response Rate by EORTC Criteria

"Tumor Response Rate by EORTC Criteria Tumor response rates were assessed from position emission tomography (PET) scans using 18F-FPPRGD2 & 18F-FDG at baseline & after 6 weeks of treatment, per European Organization for Research & Treatment of Cancer (EORTC) response criteria. The outcome is reported for each radiotracer by disease group as the number of participants achieving complete response (CR), partial response (PR), stable disease (SD), & progressive disease (PD).~CR= complete resolution of 18F-FDG uptake tumor volume~PR= reduction of 15-25% in tumor 18F-FDG SUVmax after 1 cycle of chemotherapy, and ≥25% after >1 cycle~SD= increase in tumor 18F-FDG SUVmax of <25% or a decrease of <15% & no increase in 18F-FDG tumor uptake [>20% in the longest dimension (LD)];~PD= increase in 18F-FDG tumor SUVmax of >25% in tumor region on baseline; increase in extent of 18F-FDG tumor uptake (>20% in LD); appearance of new 18F-FDG uptake in metastatic lesions" (NCT01806675)
Timeframe: At baseline and 6 weeks

,
Interventionparticipants (Number)
Complete Response (CR)Partial Repsonse (PR)Stable Disease (SD)Progressive Disease
Gynecological Cancers2101
Renal Cell Cancer (RCC)0022

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SUVmax in Which the PET-CT Was Performed Prior to the PET-MRI.

"SUVmax in FDG avid lesions in which the PET/CT was performed prior to the PET-MRI.~SUVmax is defined as [tissue concentration (MBq/g) x body weight (g)]/[injected dose (MBq/g)]" (NCT01807117)
Timeframe: Up to 6 months (each scan taking an average of 45 minutes)

InterventionSUV max (Median)
PET-CTPET-MRI
Diagnostic (PET-CT and PET-MRI)3.03.9

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True Positive Rate

"True positive rate for both modalities - TP/TP+FN~TP = true positives FN = False negatives" (NCT01807117)
Timeframe: Up to 6 months (each scan taking an average of 45 minutes)

Interventionpercentage of true positive results (Number)
PET-CTPET-MRI
Diagnostic (PET-CT and PET-MRI)7171

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True Negative Rate

"True negative rate for both modalities - TN/TN+FP~TN = true negatives FP = False positives" (NCT01807117)
Timeframe: Up to 6 months (each scan taking an average of 45 minutes)

Interventionpercent (Number)
PET-CTPET-MRI
Diagnostic (PET-CT and PET-MRI)100100

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SUVmax Ratio in Which the PET-MRI Was Performed Prior to the PET-CT

SUVmax ratio in FDG avid lesions in which the PET-MRI was performed prior to the PET-CT SUVmax is defined as [tissue concentration (MBq/g) x body weight (g)]/[injected dose (MBq/g)] (NCT01807117)
Timeframe: Up to 6 months (each scan taking an average of 45 minutes)

InterventionSUV max (Median)
PET-CTPET-MRI
Diagnostic (PET-CT and PET-MRI)2.72.0

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SUVmax Ratio in Which the PET-CT Was Performed Prior to the PET-MRI

"SUVmax ratio in FDG avid lesions in which the PET-CT was performed prior to the PET-MRI~SUVmax is defined as [tissue concentration (MBq/g) x body weight (g)]/[injected dose (MBq/g)]" (NCT01807117)
Timeframe: Up to 6 months (each scan taking an average of 45 minutes)

InterventionSUV max ratio (Median)
PET-CTPET-MRI
Diagnostic (PET-CT and PET-MRI)2.02.5

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SUVmax in Which the PET-MRI Was Performed Prior to the PET-CT

SUVmax in FDG avid lesions in which the PET-MRI was performed prior to the PET-CT SUVmax is defined as [tissue concentration (MBq/g) x body weight (g)]/[injected dose (MBq/g)] (NCT01807117)
Timeframe: Up to 6 months (each scan taking an average of 45 minutes)

InterventionSUV max (Median)
PET-CTPET-MRI
Diagnostic (PET-CT and PET-MRI)5.94.3

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Negative Predictive Values for PET-CT and PET-MRI

Percent of true negative rate of diagnostic accuracy (NCT01807117)
Timeframe: Up to 6 months (each scan taking an average of 45 minutes)

InterventionPercent of true negatives (Number)
PET-CTPET-MRI
Diagnostic (PET-CT and PET-MRI)71.4383.33

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Maximum Standardized Uptake Value (SUVmax) in Physiologic Regions and Fluorodeoxyglucose (FDG) Avid Lesions in Participants Where PET-CT Was Performed Prior to the PET-MRI

SUV max in physiologic regions (blood pool, liver) and FDG avid lesions, in which the PET-CT was performed prior to the PET-MRI. SUVmax is defined as [tissue concentration (MBq/g) x body weight (g)]/[injected dose (MBq/g)] (NCT01807117)
Timeframe: Up to 6 months (each scan taking an average of 45 minutes)

,
InterventionSUV max (Median)
PET-CTPET-MRI
Blood Pool1.91.3
Liver2.32.1

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False Negative Rate

"False negative rate for both modalities - FN/FN+TP~FN = False negatives TP = true positives" (NCT01807117)
Timeframe: Up to 6 months (each scan taking an average of 45 minutes)

Interventionpercent (Number)
PET-CTPET-MRI
Diagnostic (PET-CT and PET-MRI)2914

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Proportion of Lesions Identified by PET-CT That Were Correctly Detected by PET-MRI

On a per-lesion basis, proportion of lesions identified by PET-CT that were correctly detected by PET-MRI (NCT01807117)
Timeframe: Up to 6 months (each scan taking an average of 45 minutes)

InterventionLesions (Number)
Diagnostic (PET-CT and PET-MRI)26

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Positive Predictive Values for PET-CT and PET-MRI

Percent of true positive rate of diagnostic accuracy. (NCT01807117)
Timeframe: Up to 6 months (each scan taking an average of 45 minutes)

InterventionPercent of true positives (Number)
PET-CTPET-MRI
Diagnostic (PET-CT and PET-MRI)100100

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All Adverse Events and Complications

(NCT01821105)
Timeframe: up to 12 months

Interventionpatients (Number)
Preoperative PET and CT Scans0

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Tumor Detection

(NCT01821105)
Timeframe: At surgery

Interventionlesions detected (Number)
Preoperative PET and CT Scans48

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Detection of Position Accuracy With Handheld Probe on Anatomical Location.

(NCT01821105)
Timeframe: up to 12 months

Interventionlesions (Number)
true postivefalse positivenot evaluable
Preoperative PET and CT Scans3582

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Quantitative Amyloid Image Assessment

The effect of diagnostic group on mean total cortical grey matter florbetapir binding relative to cerebellar cortex is presented as standard uptake value ratios (SUVr). (NCT01890343)
Timeframe: 50-60 minutes after injection

InterventionSUVr (Mean)
Frontotemporal Disorder1.25
Cognitively Normal1.29
Alzheimer's Disease1.77

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Qualitative Amyloid Image Assessment

Four readers blinded to all clinical information classified florbetapir Positron Emission Tomography (PET) images as either positive for amyloid or negative for amyloid. The majority read classification is presented as either positive, negative or tied. (NCT01890343)
Timeframe: 50-60 min after injection

,,
Interventionparticipants (Number)
Positive ScanNegative ScanTie
Alzheimer's Disease820
Cognitively Normal181
Frontotemporal Disorder242

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Changes in RV Function

RV function as measured by cardiac MRI (NCT01917136)
Timeframe: 6 months

Interventionpercentage (Least Squares Mean)
11c-acetate and 18F-FDG, and Cardiac MRI7.56

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Percent Change in PET K1 Between Mid-therapy and Pre-therapy FDG PET Scans and Its Association With Pathologic Response

Percent change in tumor perfusion between pre-therapy and mid-therapy FDG PET scans as represented by the PET measure K1 (parametric) % change: (Mid-Pre)/Pre, compared between groups of patients who did or did not achieve favorable pathologic response. (NCT01931709)
Timeframe: Baseline to up to 12 weeks (mid-therapy)

Interventionpercent change (Median)
Patients With Favorable Pathologic Response-71.2
Patients Without Favorable Pathologic Response-55.8

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Time of Surgery to Overall Survival

Mean (range) (NCT01931709)
Timeframe: Overall survival from time of surgery. If death does not occur during follow-up, the endpoint will be censored at the date of last contact when the patient was verified as alive.

Interventionyears- overall survival (Mean)
Patients That Received FDG PET and DCE-MRI3.1

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Time From Surgery to Breast Cancer Recurrence

Mean (range) (NCT01931709)
Timeframe: The time from surgery to breast cancer recurrence. If recurrence does not occur during follow-up, the endpoint will be censored at the time of last documented disease-free status.

Interventionyears- recurrence free (Mean)
Patients That Received FDG PET and DCE-MRI2.9

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Percent Change in Tumor Metabolism / Perfusion Ratio (MRFDG/K1) Between Mid-therapy and Pre-therapy FDG PET Scans and Its Association With Pathologic Response

Percent change in tumor metabolism / perfusion ratio between pre-therapy and mid-therapy FDG PET scans as represented by the PET measure MRFDG/K1 (parametric) % change: (Mid-Pre)/Pre, compared between groups of patients who did or did not achieve favorable pathologic response. (NCT01931709)
Timeframe: Baseline to up to 12 weeks (mid-therapy)

Interventionpercent change (Median)
Patients With Favorable Pathologic Response-45.0
Patients Without Favorable Pathologic Response-68.5

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Number of Participants With Favorable Pathologic Response at Surgery

"The primary clinical endpoint is dichotomous (yes/no) - Has patient achieved favorable microscopic pathologic response at surgery? This favorable pathologic response is defined as:~No evidence of microscopic invasive tumor at the primary tumor site and in regional axillary lymph nodes = Residual Cancer Burden class 0 (RCB 0)~Minimal invasive residual disease at primary tumor site and/or in regional axillary lymph nodes = Residual Cancer Burden class I (RCB I)" (NCT01931709)
Timeframe: At time of surgery

InterventionParticipants (Count of Participants)
Diagnostic (FDG PET and DCE-MRI)11

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Percent Change in DCE-MRI Peak Percent Enhancement (Peak PE) Between Mid-therapy and Pre-therapy Breast MRI Scans and Its Association With Pathologic Response

Percent change in tumor enhancement between pre-therapy and mid-therapy DCE-MRI scans as represented by the MRI measure Peak PE % change: (Mid-Pre)/Pre, compared between groups of patients who did or did not achieve favorable pathologic response. (NCT01931709)
Timeframe: Baseline to up to 12 weeks (mid-therapy)

Interventionpercent change (Median)
Patients With Favorable Pathologic Response-31
Patients Without Favorable Pathologic Response-14

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Does an Inadequate Ablation Margin on PET Predict Local Progression? Compare to MRI?

Percentage of tumors with an inadequate margin on PET that progressed locally? Compare to MRI? (NCT02018107)
Timeframe: 2 Years

Interventionpercentage of tumors (Number)
PET:% local progression based on inadequate marginMRI:% local progression based on Inadequate marginPET: % local non-progression per adequate marginMRI: % local non-progression per adequate margin
N-13 Ammonia or F-18 to Image Liver PET Perfusion53.8483.3396.2989.47

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Number and Percentage of Tumors With Complete, Circumferential Ablation Margin Visibility During FDG PET/CT-guided Liver Ablations (AP-PET-1 v. Contrast-enhanced MRI)

For FDG-avid tumors, compare the rates of complete, circumferential ablation margin visibility during FDG PET/CT-guided liver ablations using two imaging techniques: intra-procedural AP-PET-1(research scan #1) and post-procedural contrast enhanced MRI . Discordance rates for complete ablation margin visibility between the two imaging techniques will be calculated. (NCT02018107)
Timeframe: 2 Years

InterventionTumors (Count of Units)
Total TumorsAssessibility of ablation margin by Pet PerfusionAssessibility of ablation margin by MRI
N-13 Ammonia or F-18 to Image Liver PET Perfusion424025

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Change in F-18 16 Alpha-fluoroestradiol (FES) Standardized Uptake Value (SUV), Assessed by a One-sample Test of the Percent Change in FES SUV

Uptake was quantified using lean body mass adjusted SUV (SULmean). The geometric mean was calculated for up to 3 lesions per patient. Systematic change in FES SULgmean between baseline and a second FES scan at approximately 2 or 8 weeks and a third FES scan was at approximately 8 weeks measured using a sign test where the median change is zero. (NCT02149173)
Timeframe: from time of first F-18 FES-PET/CT scan to time of second or third F-18 FES-PET/CT scan (approximately 2-8 weeks)

Interventionpercentage of change in SULgmean (Median)
FES-imaging After 2 Wks of ER Modulating (Vorinostat) Therapy8.7
FES-imaging After 8 Wks of ER Modulating (Vorinostat) Therapy1.9
FES-imaging After 2-8 Weeks of ER Blocking Therapy-60.3

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Proportion of Patients Experienced a Threshold in Percentage Change, or Surpassed a Targeted Follow-up F-18 16 Alpha-fluoroestradiol (FES) Standardized Uptake Value (SUV)

The number of patients showing a 20% increase in FES SULgmean compared to baseline at either 2 or 8 weeks using a 90% Wilson score binomial confidence interval. (NCT02149173)
Timeframe: from time of first F-18 FES-PET/CT scan to time of second or third F-18 FES-PET/CT scan (approximately 2-8 weeks)

InterventionProportion of participants (Number)
FES With Potential ER Modulating Therapy (Vorinostat)0
FES With Potential ER Blocking Therapy0

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F-18 16 Alpha-fluoroestradiol (FES) Uptake

Quantitative and qualitative measures of FES uptake for each disease site, a set of 1.5 cm diameter regions on three adjacent planes with the highest lesion FES uptake will be drawn to determine maximal FES uptake. Up to 10 sites seen on the static torso survey will be quantified. Lesions will qualitatively determined to be visible or not visible. (NCT02149173)
Timeframe: from time of first F-18 FES-PET/CT scan to time of second or third F-18 FES-PET/CT scan (approximately 2-8 weeks)

Interventionnumber of ER+ lesions (Count of Units)
Quantitative Uptake281
Qualitative Uptake243

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Time to Disease Progression

Months from the start of endocrine therapy to the time the patient is first recorded as having disease progression, (NCT02149173)
Timeframe: from start of therapy up to 20 years

Interventionmonths (Median)
FES With Potential ER Modulating Therapy (Vorinostat)2
FES With Potential ER Blocking Therapy5.6

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Relationship Between Tumor Minimum Uptake of Copper Cu 64-DOTA-trastuzumab as Measured by PET and Patient Best Response

Relationship between patient best response to T-DM1 and measured tumor uptake of 64Cu-DOTA-trastuzumab employed a t-test with a 0.05 two-sided significance level comparing minimum uptake in responsive vs non-responsive patients. Tumor uptake measured as SUV defined as SUV = AC(tsc) Wb /[Dinj exp(-λ(tsc - tinj)] , where AC(tsc) is the activity concentration in the volume of interest (VOI, e. g., a tumor), Wb is the patient's body weight, Dinj is the activity injected at time tinj, and λ is the decay constant for the injected radioisotope. AC(tsc) is determined from the spatial density of counts acquired from the VOI. Tumor uptake was measured in terms of minimum voxel standardized uptake value, SUVmin. Response assessment adhered to Positron Emission Tomography (PET) Response Criteria in Solid Tumors (PERCIST 1.0). (NCT02226276)
Timeframe: Up to 1 year

InterventionSUVmin (g/mL) (Median)
Diagnostic (Copper Cu 64-DOTA-trastuzumab PET)5.1

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Relationship Between Average Tumor Uptake of Copper Cu 64-DOTA-trastuzumab as Measured by PET and Patient Best Response

Relationship between patient best response to T-DM1 and measured tumor uptake of 64Cu-DOTA-trastuzumab employed a t-test with a 0.05 two-sided significance level comparing average uptake in responsive vs non-responsive patients. Tumor uptake measured as SUV defined as SUV = AC(tsc) Wb /[Dinj exp(-λ(tsc - tinj)] , where AC(tsc) is the activity concentration in the volume of interest (VOI, e. g., a tumor), Wb is the patient's body weight, Dinj is the activity injected at time tinj, and λ is the decay constant for the injected radioisotope. AC(tsc) is determined from the spatial density of counts acquired from the VOI. Tumor uptake was measured in terms of maximum voxel standardized uptake value, SUVmax. Response assessment adhered to Positron Emission Tomography (PET) Response Criteria in Solid Tumors (PERCIST 1.0). (NCT02226276)
Timeframe: Baseline

InterventionSUVmax (g/mL) (Median)
Diagnostic (Copper Cu 64-DOTA-trastuzumab PET)3.1

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Uptake of 18F-FSPG (Expressed in Maximal Standardized Uptake Value [SUV] Within the Tumor)

Maximum standardized uptake values (SUVmax) were normalized to lean body mass and measured with a 1 cm diameter round region of interest over the area of greatest uptake in the lesion being measured. (NCT02448225)
Timeframe: Up to 2 years

InterventionMaximum standardized uptake values (SUVm (Mean)
Benign Patients0.8
Cancer Patients3.9

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Ability of 18F-FSPG PET/CT to Discriminate Benign From Malignant Nodules

"Sensitivity, specificity, overall accuracy and receiver operating characteristic (ROC) curves will be generated and compared for both 18F-FDG and 18F-FSPG tests.~Sensitivity is the proportion of High(positive) among cancer patients. Specificity is the proportion of low(negative) among benign tumors. Accuracy is the proportion of correctly diagnosed among analyzed patients. Area under the curve(AUC) is the area under the ROC curve, which is the plot of sensitivity by 1-specificity." (NCT02448225)
Timeframe: Up to 2 years

Interventionproportion, range 0 to 1, higher better (Number)
FDG sensitivity(low and high)FDG specificityFDG accuracyFDG AUC(area under curve)ESPG sensitivity(low and high)ESPG specificity(low and high)ESPG accuracyESPG AUC
Diagnostic (18F-FDG PET/CT, 18F-FSPG PET/CT)0.7060.7780.7310.8170.8240.6670.7690.843

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Ability of 18F-FSPG PET/CT to Stage of Lung Cancer (Metastatic or Not)

"Sensitivity, specificity, overall accuracy and ROC curves will be generated and compared for both 18F-FDG and 18F-FSPG tests. Wilcoxon rank-sum or Kruskal-Wallis tests will be applied for the group comparisons of the biodistribution characteristics of 18F-FDG and 18F-FSPG tests.~Sensitivity is the proportion of High(positive) among cancer patients. Specificity is the proportion of low(negative) among benign tumors. Accuracy is the proportion of correctly diagnosed among all patients. Area under the curve(AUC) is the area under the ROC curve." (NCT02448225)
Timeframe: Up to 2 years

Interventionproportion, range 0-1, higher better (Number)
FDG sensitivityFDG specificityFDG accuracyFDG AUCFSPG sensitivityFSPG specificityFSPG accuracyFSPG AUC
Diagnostic (18F-FDG PET/CT, 18F-FSPG PET/CT)0.80.8570.8240.8710.20.2860.2350.8

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CD44 and xC- Expression Levels in Tissue Samples(0-3)

The level of expression of xCT and CD44 proteins in the cytoplasmic membrane of tumor cells were examined by an experienced pathologist who was blinded to any patient and imaging information. The percentage of tumor cells positive for the marker and the intensity of staining were evaluated, the latter using a scale of 0 (none), 1+ (weak), 2+ (intermediate), and 3+ (strong) with a sample being reported as positive if greater than 10% of the tumor cells in the sample were positively stained with any intensity. (NCT02448225)
Timeframe: Up to 2 years

InterventionIHC score, range 0 and above (Mean)
CD44xCT
Some Cancer Patients2.61

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Number of F-18-FDG Positive Lesions That Are Detected by the Copper Cu 64 TP3805 Analog

Cu-64 results will be compared with those of F-18-FDG for: The unit of analysis will be the lesion (with potentially multiple lesions available per patient). (NCT02810873)
Timeframe: 4 hours after Cu 64 TP3805 administered

InterventionNumber of Lesions (Number)
F-18-FDG Whole-body Scan10
No F-18-FDG Scan14

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Number of Participants With Adverse Events (AEs)

An AE was defined as any untoward medical occurrence that develops or worsens in severity during the conduct of a clinical study and does not necessarily have a causal relationship to the study drug. SAEs included death, a life-threatening AE, inpatient hospitalization or prolongation of existing hospitalization, persistent or significant disability or incapacity, a congenital anomaly or birth defect, or an important medical event that jeopardized the participant and required medical intervention to prevent 1 of the outcomes listed in this definition. A summary of serious and non-serious AEs regardless of causality is located in 'Reported Adverse Events module'. (NCT02937168)
Timeframe: 21 days

InterventionParticipants (Count of Participants)
Any AEsSAEs
Part 1: PET/CT Scan10

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Part 1: Average Global Lung Glycolysis (GLG) at Day 8

GLG is the total FDG uptake in the whole lung. ROI was drawn around lung boundary in each axial slice. SUV mean and area of each ROI was recorded. Using the formula: area*slice thickness the volume of each slice was calculated. Then the SUVmean of each slice was multiplied by the volume of the corresponding slice, which represented the total FDG uptake in one slice. This number for each slice was summed together to provide GLG of that lung. Average between GLG of right lung and GLG of left lung was reported. (NCT02937168)
Timeframe: Day 8

Interventioncm^3 (Mean)
Part 1: PET/CT Scan621.71

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Part 1: Average Global Lung Glycolysis (GLG) at Baseline (Day 1)

GLG is the total FDG uptake in the whole lung. A region of interest (ROI) was drawn around lung boundary in each axial slice. Standardized uptake value (SUV) mean and area of each ROI was recorded. Using the formula: area*slice thickness the volume of each slice was calculated. Then the SUVmean of each slice was multiplied by the volume of the corresponding slice, which represented the total FDG uptake in one slice. This number for each slice was summed together to provide GLG of that lung. Average between GLG of right lung and GLG of left lung was reported. (NCT02937168)
Timeframe: Baseline (Day 1) of Part 1

Interventioncubic centimeters (cm^3) (Mean)
Part 1: PET/CT Scan668.08

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PET/CT vs PET/MRI Difference in Standardized Uptake Value Max (SUVmax), by Radiotracer

"Standardized uptake value max (SUVmax) is a measurement of the maximum radiopharmaceutical uptake within the region of interest (ROI). Relative accuracy of a particular radiotracer in a particular tissue is determined by expressing the absolute accuracy (obtained in the primary outcome measure) in terms of percent difference between SUVmax values obtained from PET/CT and PET/MR.~Percentage difference is expressed as the difference of the means in SUVmax for the PET/CT and PET/MRI scan procedures for the particular radiotracer, divided by the mean between the values for the 2 scan procedures.~The closer the percent difference is to 0%, the better the agreement between the two scanners. The outcome is expressed as the percentage difference, a number without dispersion." (NCT03125629)
Timeframe: estimated average of 2 hours

,
InterventionPercentage difference (Number)
Aortic archGluteal muscleGluteal fatCerebellumParotid GlandLungLiverSpleen
18-FDG PET/CT and PET/MRI48.9517.343.779.422.8845.1620.697.13
68Ga DOTA-TATE PET/CT and PET/MRI5.7111.2452.6358.8218.8017.5413.6718.54

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Absolute Accuracy of SUV Max of PET/CT vs PET/MRI

Standardized uptake value max (SUVmax) is a measurement of the maximum radiopharmaceutical uptake value within the region of interest (ROI). SUVmax is calculated as the ratio of activity concentration:injected dose/body weight. The outcome is reported as the mean SUVmax with standard deviation (SD), reported for 8 specific organs or bodily locations. (NCT03125629)
Timeframe: 4 hours

,,,
Interventionratio (Mean)
Aortic archGluteal muscleGluteal fatCerebellumParotid GlandLungLiverSpleen
18F-FDG PET/CT Scan1.780.790.278.561.710.572.722.18
18F-FDG PET/MRI Scan1.080.940.267.791.760.362.212.03
68Ga-DOTA-TATE PET/CT Scan0.540.420.140.221.280.319.4713.07
68Ga-DOTA-TATE PET/MRI Scan0.510.470.240.121.060.2610.8615.74

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Complete Response (CR) With Pembrolizumab Treatment Alone

"To assess the primary objective of response rate following PET #2 performed after 3 doses of pembrolizumab. PET response will be assessed using the Lugano Criteria (2014) which recommends the 5 point Deauville score for assessing response. The Deauville five-point scale is an internationally-recommended scale for routine clinical reporting and clinical trials using FDG PET-CT in the initial staging and assessment of treatment response in Hodgkin lymphoma (HL). Patients with a Deauville score of 1-3 will be considered a complete response.~Deauville criteria is defined as follows:~No residual uptake~Slight uptake, but below blood pool (mediastinum)~Uptake above mediastinum, but below or equal to uptake in the liver~Uptake slightly to moderately higher than liver~Markedly increased uptake or any new lesions~Patients will be evaluable for response assessment if they have received at least one dose of pembrolizumab." (NCT03226249)
Timeframe: After 3 cycles of pembrolizumab (1 cycle = 21 days)

Interventionpercentage of participants (Number)
Treatment: Pembrolizumab and AVD Chemotherapy Guided by PET-CT37

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Overall Survival at Treatment Completion

Overall survival will be defined as the number of patients that are alive at the time of treatment completion (3 cycles of pembrolizumab and 2-6 cycles of AVD) (NCT03226249)
Timeframe: At completion of treatment with 3 cycles of pembrolizumab (21 day cycles) and up to 6 cycles of AVD (28 days cycles)

InterventionParticipants (Count of Participants)
Treatment: Pembrolizumab and AVD Chemotherapy Guided by PET-CT30

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Progression Free Survival (PFS) at Treatment Completion

"PFS is defined as the number of patients that are progression/relapse free at the time of treatment completion (3 cycles of pembrolizumab and up to 6 cycles of AVD).~Progressive or relapse disease is defined as of the following:~Appearance of any new lesion more than 1.5 cm in any axis during treatment, even if other lesions are decreasing in size.~At least a 50% increased from nadir in the sum of the product of the diameter (SPD) of any previously involved nodes, or in a single involved node, or the size of other lesions (e.g., splenic or hepatic nodules). To be considered progressive disease, a lymph node with a diameter of the short axis of less than 1.0 cm must increase by at least 50% and to a size of more than 1.5 x 1.5 cm or more than 1.5 cm in the long axis.~At least a 50% increase in the longest diameter of any single previously identified node more than 1.0 cm in its short axis.~Lymphoma confirmed by repeat biopsy." (NCT03226249)
Timeframe: At completion of treatment with 3 cycles of pembrolizumab (21 day cycles) and up to 6 cycles of AVD (28 days cycles)

InterventionParticipants (Count of Participants)
Treatment: Pembrolizumab and AVD Chemotherapy Guided by PET-CT30

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Visual Image Analysis of Detected Multiple Myeloma Lesions

The visual image analysis scale has a range of 0-4: (0 no uptake; 1 benign, 2 probably benign, 3 probably malignant, 4 malignant). (NCT03262389)
Timeframe: Approximately one month after Day 2

Interventionscore on a scale (Mean)
C-11 acetate PET CTC-11 acetate PET MRI18 FDG PET CT18 FDG PET MRI
Multiple Myeloma (MM) Patients3.13.31.92.0

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Mean Multiple Myeloma Lesions Detected

The number of lesions detected in the scans will be averaged for each technique. Two techniques (scans) will be tested on Day 1 and two techniques (scans) will be tested on Day 2. (NCT03262389)
Timeframe: Day 1, Day 2

Interventionnumber of lesions (Mean)
C-11 acetate PET CTC-11 acetate PET MRI18 FDG PET CT18 FDG PET MRI
Multiple Myeloma (MM) Patients4.64.41.11.0

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Change in SUVpeak of Target Lesions Between Infiltrated and Non-infiltrated Scans

Target lesions selected as per PERCIST criteria. These criteria require more space than allowed to explain. Reference J Nucl Med 2009; 50: 122S-150S. DOI: 10.2967/jnumed.108.057307 (NCT03320564)
Timeframe: Baseline scan and follow up scan within 7 days

InterventionSUV (dimensionless) (Mean)
Infiltration3.6

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13NH3 PET/CT Uptake With Cardia Sarcoidosis (CS)

The number of subjects with areas of perfusion deficits on 13NH3 PET/CT scan (NCT03549598)
Timeframe: 2 days

InterventionParticipants (Count of Participants)
68Ga-DOTATATE PET/CT8

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18FDG Uptake With Cardia Sarcoidosis (CS)

The number of subjects with areas of abnormal myocardial increased focal uptake on 18FDG scan (NCT03549598)
Timeframe: 2 days

InterventionParticipants (Count of Participants)
68Ga-DOTATATE PET/CT9

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F-18 16 Alpha-fluoroestradiol (FES) Uptake

Quantitative measures of FES uptake for each disease site will be determined by drawing regions-of-interest on lesions to determine maximal FES uptake (SUVmax) per lesion. Up to 10 sites seen on the static torso survey will be quantified. (NCT04692103)
Timeframe: From time of first F-18 FES-PET/CT scan to time of second F-18 FES-PET/CT scan (approximately 1-12 weeks)

Interventionaverage SUVmax (Mean)
FES scan 1FES scan 2
Diagnostic (F-18 FES PET/CT)5.71.4

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Proportion of Patients With a Threshold of Percentage Change, or That Surpass a Targeted Follow-up F-18 16 Alpha-fluoroestradiol (FES) Standardized Uptake Value (SUV)

The number of patients showing a 20% increase in FES uptake (SULmean or SUVmax) compared to baseline from the first to second scan using a 90% Wilson score binomial confidence interval. (NCT04692103)
Timeframe: From time of first F-18 FES-PET/CT scan to time of second F-18 FES-PET/CT scan (approximately 1-12 weeks)

Interventionparticipants with increased FES uptake (Number)
Diagnostic (F-18 FES PET/CT)0

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Change in F-18 16 Alpha-fluoroestradiol (FES) Standardized Uptake Value (SUV) - Avg SULmax

FES uptake will be quantified using lean body mass adjusted SUV (SUL). Percentage change in FES average SULmax between baseline and a second FES scan will be calculated for up to 3 lesions per patient. (NCT04692103)
Timeframe: From time of first F-18 FES-PET/CT scan to time of second F-18 FES-PET/CT scan (approximately 1-12 weeks)

InterventionPercentage decrease in avgSUL (Mean)
Diagnostic (F-18 FES PET/CT)78

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