niacinamide has been researched along with Thyroid Neoplasms in 165 studies
nicotinamide : A pyridinecarboxamide that is pyridine in which the hydrogen at position 3 is replaced by a carboxamide group.
Thyroid Neoplasms: Tumors or cancer of the THYROID GLAND.
Excerpt | Relevance | Reference |
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" Toxicity was manageable and as previously described for sorafenib, including hypertension and skin rash." | 9.17 | Phase II trial of sorafenib in patients with advanced anaplastic carcinoma of the thyroid. ( Chapman, R; Dowlati, A; Fu, P; Lavertu, P; Nagaiah, G; Remick, SC; Savvides, P; Wasman, J; Wright, JJ, 2013) |
"Sorafenib has shown promise in the treatment of patients with advanced or metastatic thyroid carcinoma." | 9.15 | Response to sorafenib at a low dose in patients with radioiodine-refractory pulmonary metastases from papillary thyroid carcinoma. ( Chen, L; Lu, H; Luo, Q; Shen, Y; Yu, Y; Zhu, R, 2011) |
"We measured serum thyroxine (T4), free T4, 3,5,3-triiodothyronine (T3), free T3, reverse T3 (rT3), and TSH concentrations at baseline and after 26 wk in 21 patients with progressive nonmedullary thyroid carcinoma treated with sorafenib." | 9.14 | Sorafenib-induced hypothyroidism is associated with increased type 3 deiodination. ( Abdulrahman, RM; Corssmit, EP; Gelderblom, H; Hoftijzer, H; Hovens, GC; Kapiteijn, E; Pereira, AM; Reiners, C; Romijn, JA; Smit, JW; Verburg, E; Verloop, H; Visser, TJ, 2010) |
" Sorafenib treatment was associated with Cushing's syndrome remission, elevated progesterone (>10 fold), normalization of dehydroepiandrostenedione sulfate, but persistently elevated cortisol concentration." | 7.81 | Case report of severe Cushing's syndrome in medullary thyroid cancer complicated by functional diabetes insipidus, aortic dissection, jejunal intussusception, and paraneoplastic dysautonomia: remission with sorafenib without reduction in cortisol concentr ( Abouzied, Mel-D; Aklabi, S; Duaiji, N; Hammami, MM; Mutairi, G; Qattan, N; Sous, MW, 2015) |
" Sorafenib is a small-molecule multikinase inhibitor used in radioactive iodine ((131)I)-refractive papillary thyroid carcinoma." | 7.80 | Response to sorafenib in a pediatric patient with papillary thyroid carcinoma with diffuse nodular pulmonary disease requiring mechanical ventilation. ( Ewig, JM; Iyer, P; Mayer, JL, 2014) |
" Here, we report a radioiodine-refractory follicular thyroid carcinoma (FTC) patient in whom a notable decrease of MPE was achieved after treatment with sorafenib." | 7.80 | Notable decrease of malignant pleural effusion after treatment with sorafenib in radioiodine-refractory follicular thyroid carcinoma. ( Chen, L; Li, M; Liu, M; Ruan, M; Shen, Y, 2014) |
" We report a case of a 60-year-old woman who developed left renal artery stenosis associated with renal atrophy in the context of metastatic papillary thyroid carcinoma treated with sorafenib." | 7.79 | Unilateral renal artery stenosis with renal atrophy in a patient with metastatic papillary thyroid carcinoma treated with sorafenib. ( Busaidy, NL; Habra, MA; Schellingerhout, D; Shawa, H, 2013) |
"Sorafenib has clinically relevant antitumor activity in patients with progressive metastatic or locally advanced radio-iodine refractory differentiated thyroid cancer." | 6.77 | Long-term analysis of the efficacy and tolerability of sorafenib in advanced radio-iodine refractory differentiated thyroid carcinoma: final results of a phase II trial. ( Abdulrahman, RM; Corssmit, EP; Kapiteijn, E; Morreau, H; Schneider, TC; Smit, JW, 2012) |
" However, adverse effects common to the tyrosine kinase inhibitor class occur at a noticeably higher rate with sorafenib use in thyroid cancer patients." | 6.53 | Toxic Effects of Sorafenib in Patients With Differentiated Thyroid Carcinoma Compared With Other Cancers. ( Jaffry, A; Jean, GW; Khan, SA; Mani, RM, 2016) |
"Sorafenib was recently approved for the treatment of these patients." | 5.42 | Partial response to sorafenib treatment associated with transient grade 3 thrombocytopenia in a patient with locally advanced thyroid cancer. ( Abelleira, E; Cross, G; Jerkovich, F; Pitoia, F; Urciuoli, C, 2015) |
"Sorafenib has shown promise in the treatment of patients with advanced or metastatic thyroid carcinoma." | 5.38 | Brain metastasis from follicular thyroid carcinoma: treatment with sorafenib. ( Chen, L; Lu, H; Luo, Q; Ruan, M; Shen, Y; Yu, Y; Zhu, R, 2012) |
"Everolimus was neither additive nor syngergistic in combination with sorafenib or AZD6244." | 5.38 | Sorafenib and Mek inhibition is synergistic in medullary thyroid carcinoma in vitro. ( Agarwal, K; Brendel, VJ; Jarjoura, D; Koh, YW; Koo, BS; McCarty, SK; Porter, K; Ringel, MD; Saji, M; Shah, MH; Wang, C, 2012) |
" Toxicity was manageable and as previously described for sorafenib, including hypertension and skin rash." | 5.17 | Phase II trial of sorafenib in patients with advanced anaplastic carcinoma of the thyroid. ( Chapman, R; Dowlati, A; Fu, P; Lavertu, P; Nagaiah, G; Remick, SC; Savvides, P; Wasman, J; Wright, JJ, 2013) |
"Sorafenib has shown promise in the treatment of patients with advanced or metastatic thyroid carcinoma." | 5.15 | Response to sorafenib at a low dose in patients with radioiodine-refractory pulmonary metastases from papillary thyroid carcinoma. ( Chen, L; Lu, H; Luo, Q; Shen, Y; Yu, Y; Zhu, R, 2011) |
"To evaluate the tolerability and efficacy of sorafenib in patients with thyroid carcinoma." | 5.15 | Analysis of the efficacy and toxicity of sorafenib in thyroid cancer: a phase II study in a UK based population. ( Ahmed, M; Barbachano, Y; Harrington, KJ; Hickey, J; Marais, R; Newbold, KL; Nutting, CM; Riddell, A; Viros, A, 2011) |
"We measured serum thyroxine (T4), free T4, 3,5,3-triiodothyronine (T3), free T3, reverse T3 (rT3), and TSH concentrations at baseline and after 26 wk in 21 patients with progressive nonmedullary thyroid carcinoma treated with sorafenib." | 5.14 | Sorafenib-induced hypothyroidism is associated with increased type 3 deiodination. ( Abdulrahman, RM; Corssmit, EP; Gelderblom, H; Hoftijzer, H; Hovens, GC; Kapiteijn, E; Pereira, AM; Reiners, C; Romijn, JA; Smit, JW; Verburg, E; Verloop, H; Visser, TJ, 2010) |
" In endocrine tumors, several molecules have demonstrated efficacy in terms of progression free survival during phase III trials such as vandetanib and cabozantinib in medullary thyroid carcinoma, sorafenib in differentiated thyroid carcinoma and everolimus or sunitinib for pancreatic neuroendocrine tumors." | 4.89 | [Targeted therapies, prognostic and predictive factors in endocrine oncology]. ( Baudin, E; Borson-Chazot, F; Hescot, S; Lombès, M, 2013) |
"Sorafenib is an oral multikinase inhibitor with regulatory approval in advanced renal cell carcinoma (RCC), hepatocellular carcinoma (HCC) and refractory differentiated thyroid carcinoma (DTC)." | 4.12 | Effectiveness and safety of sorafenib for renal cell, hepatocellular and thyroid carcinoma: pooled analysis in patients with renal impairment. ( Imai, T; Kaneko, S; Okayama, Y; Oya, M; Sunaya, T; Tsujino, T, 2022) |
"Sorafenib (BAY 43-9006) is an inhibitor of multiple-receptor tyrosine kinases involved in tumor growth and angiogenesis, which can be advantageously administered orally." | 3.85 | Sorafenib: rays of hope in thyroid cancer. ( Bernardini, R; Duntas, LH, 2010) |
"Sorafenib, a multikinase inhibitor has recently been approved for the treatment of radio-iodine refractory thyroid carcinoma." | 3.81 | Synergistic anti-proliferative effect of metformin and sorafenib on growth of anaplastic thyroid cancer cells and their stem cells. ( Chen, G; Derwahl, M; Nicula, D; Renko, K, 2015) |
" Sorafenib treatment was associated with Cushing's syndrome remission, elevated progesterone (>10 fold), normalization of dehydroepiandrostenedione sulfate, but persistently elevated cortisol concentration." | 3.81 | Case report of severe Cushing's syndrome in medullary thyroid cancer complicated by functional diabetes insipidus, aortic dissection, jejunal intussusception, and paraneoplastic dysautonomia: remission with sorafenib without reduction in cortisol concentr ( Abouzied, Mel-D; Aklabi, S; Duaiji, N; Hammami, MM; Mutairi, G; Qattan, N; Sous, MW, 2015) |
" Sorafenib is a small-molecule multikinase inhibitor used in radioactive iodine ((131)I)-refractive papillary thyroid carcinoma." | 3.80 | Response to sorafenib in a pediatric patient with papillary thyroid carcinoma with diffuse nodular pulmonary disease requiring mechanical ventilation. ( Ewig, JM; Iyer, P; Mayer, JL, 2014) |
"THERE WERE 62 PATIENTS (37 MEN, MEAN AGE: 61 years) treated with sorafenib (62%), sunitinib (22%), and vandetanib (16%) outside of clinical trials; 22 had papillary, five had follicular, five had Hürthle cell, 13 had poorly differentiated, and 17 had medullary thyroid carcinoma (MTC)." | 3.80 | Tyrosine kinase inhibitor treatments in patients with metastatic thyroid carcinomas: a retrospective study of the TUTHYREF network. ( Baudin, E; Bonichon, F; Borget, I; Brassard, M; Chougnet, CN; Claude-Desroches, M; de la Fouchardière, C; Do Cao, C; Giraudet, AL; Leboulleux, S; Massicotte, MH; Schlumberger, M, 2014) |
" Here, we report a radioiodine-refractory follicular thyroid carcinoma (FTC) patient in whom a notable decrease of MPE was achieved after treatment with sorafenib." | 3.80 | Notable decrease of malignant pleural effusion after treatment with sorafenib in radioiodine-refractory follicular thyroid carcinoma. ( Chen, L; Li, M; Liu, M; Ruan, M; Shen, Y, 2014) |
" The relative role of such novel radiopharmaceutical versus (131)I scanning of thyroid cancer will require future histopathologic and clinical studies, but it may open new perspectives for presurgical staging of thyroid cancer, and diagnosis of radioiodine negative local relapses and/or distant metastases." | 3.80 | (99m)Tc-labeled-rhTSH analogue (TR1401) for imaging poorly differentiated metastatic thyroid cancer. ( Balogh, L; Dierckx, RA; Fremont, V; Galli, F; Manni, I; Piaggio, G; Signore, A; Szkudlinski, MW; Weintraub, BD, 2014) |
"Before and after the last week of sorafenib therapy, 20 patients with progressive differentiated thyroid carcinoma received a standard dose regimen of two injections 0." | 3.79 | Sorafenib therapy decreases the clearance of thyrotropin. ( Dekkers, OM; Smit, JW; Verloop, H, 2013) |
" We report a case of a 60-year-old woman who developed left renal artery stenosis associated with renal atrophy in the context of metastatic papillary thyroid carcinoma treated with sorafenib." | 3.79 | Unilateral renal artery stenosis with renal atrophy in a patient with metastatic papillary thyroid carcinoma treated with sorafenib. ( Busaidy, NL; Habra, MA; Schellingerhout, D; Shawa, H, 2013) |
"In a randomized phase III clinical trial, patients with metastatic differentiated cancer of the thyroid who were treated with sorafenib achieved median progression-free survival of 10." | 3.79 | Sorafenib makes headway on metastatic thyroid cancer. ( , 2013) |
"Sorafenib is an oral multikinase inhibitor approved for the treatment of patients with radioactive iodine-refractory differentiated thyroid cancer (DTC)." | 2.84 | Sorafenib in Japanese Patients with Locally Advanced or Metastatic Medullary Thyroid Carcinoma and Anaplastic Thyroid Carcinoma. ( Ito, KI; Ito, Y; Kabu, K; Onoda, N; Sugitani, I; Takahashi, S; Tsukada, K; Yamaguchi, I, 2017) |
"One of 2 patients with anaplastic thyroid cancer had an objective response." | 2.84 | Phase 2 study evaluating the combination of sorafenib and temsirolimus in the treatment of radioactive iodine-refractory thyroid cancer. ( Baxi, SS; Cullen, G; Dunn, LA; Fagin, JA; Fury, MG; Ghossein, RA; Haque, S; Ho, AL; Pfister, DG; Sherman, EJ; Sima, CS, 2017) |
"Effective adverse event (AE) management is critical to maintaining patients on anticancer therapies." | 2.80 | Safety and tolerability of sorafenib in patients with radioiodine-refractory thyroid cancer. ( Ando, Y; Bonichon, F; Brose, MS; Chung, J; Fassnacht, M; Fugazzola, L; Gao, M; Hadjieva, T; Hasegawa, Y; Kappeler, C; Meinhardt, G; Park, DJ; Schlumberger, M; Shi, Y; Shong, YK; Smit, JW; Worden, F, 2015) |
"Patients with advanced thyroid cancer derived meaningful clinical benefit from additional therapy with a biologic agent following disease progression on front-line targeted therapy." | 2.78 | Clinical efficacy of targeted biologic agents as second-line therapy of advanced thyroid cancer. ( Chen, Z; Chowdry, RP; Khuri, FR; Kim, S; Owonikoko, TK; Saba, NF; Shin, DM, 2013) |
"Sorafenib has clinically relevant antitumor activity in patients with progressive metastatic or locally advanced radio-iodine refractory differentiated thyroid cancer." | 2.77 | Long-term analysis of the efficacy and tolerability of sorafenib in advanced radio-iodine refractory differentiated thyroid carcinoma: final results of a phase II trial. ( Abdulrahman, RM; Corssmit, EP; Kapiteijn, E; Morreau, H; Schneider, TC; Smit, JW, 2012) |
"Sorafenib is a multikinase inhibitor that targets several molecular signals believed to be involved in the pathogenesis of thyroid cancer, including those implicated in DTC." | 2.76 | Rationale and design of decision: a double-blind, randomized, placebo-controlled phase III trial evaluating the efficacy and safety of sorafenib in patients with locally advanced or metastatic radioactive iodine (RAI)-refractory, differentiated thyroid ca ( Brose, MS; Chung, J; Kalmus, J; Kappeler, C; Nutting, CM; Reike, G; Schlumberger, M; Sherman, SI; Shong, YK; Smit, JW, 2011) |
" The most common treatment-related adverse events were diarrhea (41%), fatigue (41%), hypothyroidism (29%), hypertension (27%), and anorexia (27%)." | 2.74 | Phase II study of safety and efficacy of motesanib in patients with progressive or symptomatic, advanced or metastatic medullary thyroid cancer. ( Bastholt, L; Daumerie, C; Droz, JP; Elisei, R; Eschenberg, MJ; Jarzab, B; Juan, T; Locati, LD; Martins, RG; Pacini, F; Schlumberger, MJ; Sherman, SI; Stepan, DE; Sun, YN; Wirth, LJ, 2009) |
"Sorafenib has a beneficial effect on tumor progression in patients with metastatic DTC, but was less effective in patients with bone metastases." | 2.74 | Beneficial effects of sorafenib on tumor progression, but not on radioiodine uptake, in patients with differentiated thyroid carcinoma. ( Corssmit, EP; Gelderblom, H; Heemstra, KA; Hoftijzer, H; Huijberts, M; Kapiteijn, E; Morreau, H; Pereira, AM; Romijn, JA; Smit, JW; Stokkel, MP; Weijers, K, 2009) |
"Sorafenib has clinically relevant antitumor activity in patients with metastatic, iodine-refractory thyroid carcinoma, with an overall clinical benefit rate (partial response + stable disease) of 77%, median PFS of 79 weeks, and an overall acceptable safety profile." | 2.73 | Phase II trial of sorafenib in advanced thyroid cancer. ( Brose, MS; Flaherty, KT; Gupta-Abramson, V; Loevner, LA; Mandel, SJ; Nellore, A; O'Dwyer, PJ; Puttaswamy, K; Ransone, K; Redlinger, M; Troxel, AB, 2008) |
"Sorafenib (Nexavar), is a multikinase inhibitor, which has demonstrated both antiproliferative and antiangiogenic properties in vitro and in vivo, inhibiting the activity of targets present in the tumoral cells (c-RAF [proto-oncogene serine/threonine-protein kinase], BRAF, (V600E)BRAF, c-KIT, and FMS-like tyrosine kinase 3) and in tumor vessels (c-RAF, vascular endothelial growth factor receptor [VEGFR]-2, VEGFR-3, and platelet-derived growth factor receptor β)." | 2.55 | Aggressive thyroid cancer: targeted therapy with sorafenib. ( Antonelli, A; Corrado, A; Fallahi, P; Ferrari, SM; Materazzi, G; Mazzi, V; Miccoli, M; Miccoli, P; Politti, U; Ulisse, S, 2017) |
"Distant metastases from differentiated thyroid cancer (DTC) are a rare event, occurring in less than 10% of patients with persistent or recurrent clinical disease." | 2.55 | Which patient with thyroid cancer deserves systemic therapy and when? ( Pacini, F, 2017) |
" However, adverse effects common to the tyrosine kinase inhibitor class occur at a noticeably higher rate with sorafenib use in thyroid cancer patients." | 2.53 | Toxic Effects of Sorafenib in Patients With Differentiated Thyroid Carcinoma Compared With Other Cancers. ( Jaffry, A; Jean, GW; Khan, SA; Mani, RM, 2016) |
"Treatment of differentiated thyroid cancer consists of surgery followed by radioactive iodine (RAI) ablation of the thyroid remnant, and TSH suppression." | 2.53 | Lenvatinib for the treatment of radioiodine-refractory differentiated thyroid carcinoma: a systematic review and indirect comparison with sorafenib. ( Brzostek, T; Kawalec, P; Kózka, M; Malinowska-Lipień, I, 2016) |
"Sorafenib is a multiple kinase inhibitor (MKI) approved for the treatment of primary advanced renal cell carcinoma and advanced primary liver cancer." | 2.53 | Selective use of sorafenib in the treatment of thyroid cancer. ( Jerkovich, F; Pitoia, F, 2016) |
"Differentiated thyroid cancer is the most common endocrine malignancy, and its incidence has been rising rapidly over the past 10 years." | 2.52 | Targeted therapies in advanced differentiated thyroid cancer. ( Agulnik, M; Carneiro, BA; Carneiro, RM; Giles, FJ; Kopp, PA, 2015) |
"Sorafenib is an oral multikinase inhibitor with anticancer activity against a wide spectrum of cancers." | 2.52 | Sorafenib: 10 years after the first pivotal trial. ( Abbate, I; Brandi, M; De Rose, F; Divella, R; Ferraro, E; Filippelli, G; Gadaleta-Caldarola, G; Infusino, S; Mazzocca, A, 2015) |
"Advanced thyroid cancer is not amenable to therapy with conventional cytotoxic chemotherapy." | 2.52 | Treatment of advanced thyroid cancer: role of molecularly targeted therapies. ( Covell, LL; Ganti, AK, 2015) |
"Sorafenib (Nexavar) is an oral multi-kinase inhibitor targeting B-type Raf kinase (BRAF) (both wild type and BRAF(V600E)), VEGFR1, VEGFR2, VEGFR3, PDGFRβ and RET (also RET/PTC) influencing both differentiated thyroid cancer (DTC) cell proliferation and angiogenesis." | 2.52 | Sorafenib for the treatment of thyroid cancer: an updated review. ( Handkiewicz-Junak, D; Jarzab, B; Krajewska, J, 2015) |
"The treatment of differentiated thyroid cancer refractory to radioactive iodine (RAI) had been hampered by few effective therapies." | 2.52 | Differentiated thyroid cancer: focus on emerging treatments for radioactive iodine-refractory patients. ( Colevas, AD; Gruber, JJ, 2015) |
"Sorafenib was specifically developed to target rapidly accelerated fibrosarcoma (RAF) kinase in the MAPK pathway." | 2.52 | The discovery and development of sorafenib for the treatment of thyroid cancer. ( Cohen, MS; White, PT, 2015) |
"Radio-iodine refractory metastatic thyroid cancers are rare and their management was until recently relatively complex." | 2.52 | Targeted treatments of radio-iodine refractory differentiated thyroid cancer. ( de la Fouchardière, C, 2015) |
"Treatment with sorafenib in patients with progressive DTC and MTC is a promising strategy, but the adverse event rate is high, leading to a high rate of dose reduction or discontinuation." | 2.50 | Sorafenib in metastatic thyroid cancer: a systematic review. ( Cabanillas, ME; Dadu, R; Dong, W; Feng, L; Lai, SY; Regone, RM; Thomas, L, 2014) |
"Sorafenib (Nexavar) is a multikinase inhibitor, which has demonstrated both anti-proliferative and anti-angiogenic properties in vitro and in vivo, inhibiting the activity of targets present in the tumor cell [c-RAF (proto-oncogene serine/threonine-protein kinase), BRAF, (V600E)BRAF, c-KIT, and FMS-like tyrosine kinase 3] and in tumor vessels (c-RAF, vascular endothelial growth factor receptor-2, vascular endothelial growth factor receptor-3, and platelet-derived growth factor receptor β)." | 2.49 | Sorafenib and thyroid cancer. ( Antonelli, A; Corrado, A; Fallahi, P; Ferrari, SM; Materazzi, G; Miccoli, P; Santini, F; Ulisse, S, 2013) |
"The incidence of thyroid cancer continues to increase and this neoplasia remains the most common endocrine malignancy." | 2.48 | Novel molecular targeted therapies for refractory thyroid cancer. ( Arango, BA; Cohen, EE; Perez, CA; Raez, LE; Santos, ES, 2012) |
"The prognosis of almost all thyroid cancers is good, but some patients have indications for these molecularly targeted drugs." | 2.47 | Current status of molecularly targeted drugs for the treatment of advanced thyroid cancer. ( Takami, HE, 2011) |
"Medullary thyroid carcinoma has a worse prognosis, especially in patients with diffused cancers at the time of initial surgery." | 2.45 | Targeted molecular therapies in thyroid carcinoma. ( Moretti, S; Puxeddu, E; Romagnoli, S; Voce, P, 2009) |
"PTC represents 80-90% of all thyroid cancers and over the past five years, more than 200 manuscripts have been published about the relationship between "B-Raf(V600E) and thyroid cancer"." | 2.45 | Role of B-Raf(V600E) in differentiated thyroid cancer and preclinical validation of compounds against B-Raf(V600E). ( Goldfarb, M; Hodin, R; Nucera, C; Parangi, S, 2009) |
"Treatment of patients with thyroid cancer is usually successful, and most patients are cured of the disease." | 2.42 | How thyroid tumors start and why it matters: kinase mutants as targets for solid cancer pharmacotherapy. ( Fagin, JA, 2004) |
"Chloroquine (CQ) is an autophagy inhibitor that has been reported to increase sensitivity to various cancer treatments." | 1.48 | Inhibition of autophagy enhances the targeted therapeutic effect of sorafenib in thyroid cancer. ( Ge, M; Jin, S; Li, L; Long, B; Yang, M; Ye, T; Ye, X; Yi, H; Zhang, L, 2018) |
"Treatment with sorafenib was initiated, resulting in significant tumor reduction allowing near total thyroidectomy and bilateral neck dissection." | 1.48 | Potential role of sorafenib as neoadjuvant therapy in unresectable papillary thyroid cancer. ( Bonani, FA; Camargo, RY; Castro, G; Coura-Filho, GB; Danilovic, DLS; Freitas, RMC; Hoff, AO; Kulcsar, MA; Marui, S; Roitberg, FSR; Vanderlei, FAB, 2018) |
" Additional secondary endpoints are postprogression survival from time of symptomatic progression, duration of and response to each systemic treatment regimen and dosing of sorafenib throughout the treatment period." | 1.46 | Timing of multikinase inhibitor initiation in differentiated thyroid cancer. ( Brose, MS; DeSanctis, Y; Fellous, M; Lin, CC; Pitoia, F; Schlumberger, M; Smit, J; Sugitani, I; Tori, M, 2017) |
"Sorafenib is a multikinase inhibitor of RTKs and the MAPK pathway and has recently been used for the treatment of unresectable well-differentiated thyroid carcinoma." | 1.46 | Effects of sorafenib and an adenylyl cyclase activator on in vitro growth of well-differentiated thyroid cancer cells. ( Chiba, T; Hara, H; Ishii, J; Kamma, H; Sawa, A; Yamamoto, H, 2017) |
"Anaplastic thyroid cancer (ATC) comprises approximately 2% of all thyroid cancers, and its median survival rate remains poor." | 1.43 | Sorafenib and Quinacrine Target Anti-Apoptotic Protein MCL1: A Poor Prognostic Marker in Anaplastic Thyroid Cancer (ATC). ( Abdulghani, J; Cooper, T; Derr, J; Dicker, D; El-Deiry, WS; Finnberg, NK; Gallant, JN; Gokare, P; Goldenberg, D; Liao, J; Liu, J; Whitcomb, T, 2016) |
"Lenvatinib is an oral potent multi kinase inhibitor [MKI] of different growth factor receptors including VEGFR1/Flt-1, VEGFR2/KDR, VEGFR3, FGFR1,2,3,4, PDGFR-β as well as RET and KIT signaling networks." | 1.43 | Efficacy of lenvatinib in treating thyroid cancer. ( Jarzab, B; Krajewska, J; Kukulska, A, 2016) |
"Sorafenib treatment could be considered when vandetanib and cabozantinib are not available or after failing these drugs." | 1.43 | Sorafenib for the Treatment of Progressive Metastatic Medullary Thyroid Cancer: Efficacy and Safety Analysis. ( de Castro, G; de Castroneves, LA; de Freitas, RM; Fukushima, JT; Hoff, AO; Hoff, PM; Jorge, AA; Kulcsar, MA; Lima, JV; Negrão, MV; Papadia, C; Simão, EF; Tavares, MR, 2016) |
"Differentiated thyroid cancers are usually cured by an appropriate surgery and a radioiodine remnant ablation." | 1.43 | [Lenvatinib in radioiodine refractory thyroid carcinomas]. ( de la Fouchardiere, C, 2016) |
" In BRAF-mutant melanomas, orally bioavailable B-Raf inhibitors, such as vemurafenib, achieve dramatic responses initially, but this is followed by rapid emergence of resistance driven by numerous mechanisms and requiring second-generation treatment approaches." | 1.43 | B-Raf Inhibition in the Clinic: Present and Future. ( Fiskus, W; Mitsiades, N, 2016) |
"The curcumin was found to dose-dependently inhibit the apoptosis of FTC133 cells possibly via PI3K/Akt and ERK pathways." | 1.43 | Combinatorial anticancer effects of curcumin and sorafenib towards thyroid cancer cells via PI3K/Akt and ERK pathways. ( Chen, W; Lv, Y; Xie, R; Yu, J; Zhang, J, 2016) |
"Sorafenib has an antitumor activity in patients with radioactive iodine-refractory differentiated thyroid carcinoma (RAIR-DTC)." | 1.43 | pAKT Expression and Response to Sorafenib in Differentiated Thyroid Cancer. ( Brose, MS; Chen, EY; Cohen, AB; Feldman, MD; Johnson, BA; Ma, C; Pappas-Paxinos, M; Stopenski, SJ; Tang, W; Troxel, AB; Yarchoan, M, 2016) |
"Sorafenib is an orally active multikinase tyrosine kinase inhibitor (TKI) that targets B-type Raf kinase (BRAF), vascular endothelial growth factor receptors (VEGFR) 1 and 2, and rearranged during transfection (RET), inducing anti-angiogenic and pro-apoptotic actions in a wide range of solid tumors." | 1.43 | (Secondary) solid tumors in thyroid cancer patients treated with the multi-kinase inhibitor sorafenib may present diagnostic challenges. ( Kapiteijn, E; Morreau, H; Schneider, TC; Smit, JWA; van der Hoeven, JJM; van Wezel, T, 2016) |
"Sorafenib was recently approved for the treatment of these patients." | 1.42 | Partial response to sorafenib treatment associated with transient grade 3 thrombocytopenia in a patient with locally advanced thyroid cancer. ( Abelleira, E; Cross, G; Jerkovich, F; Pitoia, F; Urciuoli, C, 2015) |
"Pretreatment with sorafenib also inhibited PBMC expression of IFN-α- and IL-2-regulated genes and inhibited NK cell production of IFN-γ, RANTES, MIP1-α, and MIG in response to IFN-α stimulation." | 1.42 | The Raf Kinase Inhibitor Sorafenib Inhibits JAK-STAT Signal Transduction in Human Immune Cells. ( Byrd, JC; Caligiuri, MA; Campbell, AR; Carson, WE; Fairchild, ET; Grignol, VP; Guenterberg, KD; Jaime-Ramirez, AC; Karpa, VI; Kondadasula, SV; Lesinski, GB; Levine, KM; Mace, TA; Markowitz, J; Martin del Campo, SE; McClory, S; Monk, JP; Mortazavi, A; Mundy-Bosse, BL; Olencki, TE; Pan, X; Paul, BK; Shah, MH; Tridandapani, S; Trikha, P, 2015) |
"Sorafenib treatment caused a rapid inhibition of various MAP kinases in addition to inhibiting AKT and receptor tyrosine kinases." | 1.42 | Sorafenib inhibits intracellular signaling pathways and induces cell cycle arrest and cell death in thyroid carcinoma cells irrespective of histological origin or BRAF mutational status. ( Britten, M; Broecker-Preuss, M; Fuhrer, D; Mann, K; Müller, S; Schmid, KW; Worm, K, 2015) |
"Sorafenib has been evaluated in several Phase II and III studies in patients with locally advanced/metastatic radioactive iodine-refractory differentiated thyroid carcinomas (DTCs), reporting partial responses, stabilization of the disease and improvement of progression-free survival." | 1.42 | Sorafenib in the treatment of thyroid cancer. ( Antonelli, A; Baldini, E; Fallahi, P; Ferrari, SM; Materazzi, G; Miccoli, P; Politti, U; Spisni, R; Ulisse, S, 2015) |
"Kinase inhibitor therapy may be used to treat thyroid carcinoma that is symptomatic and/or progressive and not amenable to treatment with radioactive iodine." | 1.40 | Thyroid carcinoma, version 2.2014. ( Ball, DW; Byrd, D; Dickson, P; Duh, QY; Ehya, H; Haddad, RI; Haymart, M; Hoffmann, KG; Hoh, C; Hughes, M; Hunt, JP; Iagaru, A; Kandeel, F; Kopp, P; Lamonica, DM; Lydiatt, WM; McCaffrey, J; Moley, JF; Parks, L; Raeburn, CD; Ridge, JA; Ringel, MD; Scheri, RP; Shah, JP; Sherman, SI; Sturgeon, C; Tuttle, RM; Waguespack, SG; Wang, TN; Wirth, LJ, 2014) |
"Treatment with sorafenib 400 mg twice a day was initiated resulting in a rapid and significant reduction of cortisol and ACTH levels associated with dramatic clinical improvement." | 1.40 | Complete resolution of hypercortisolism with sorafenib in a patient with advanced medullary thyroid carcinoma and ectopic ACTH (adrenocorticotropic hormone) syndrome. ( Barroso-Sousa, R; Evangelista, J; Fragoso, MC; Hoff, AO; Kulcsar, MA; Lerario, AM; Lin, CS; Lourenço, DM; Papadia, C, 2014) |
"Sorafenib doses were increased up to 1600 mg bid, in order to maintain clinical activity, and to restore active plasma concentration, since sorafenib exposure had decreased over the time." | 1.40 | Critical role of sorafenib exposure over time for its antitumor activity in thyroid cancer. ( Bellesoeur, A; Billemont, B; Blanchet, B; Carton, E; Clerc, J; Goldwasser, F; Groussin, L; Mir, O, 2014) |
"Sorafenib has recently been recognized as an important standard option for the management of patients with differentiated thyroid cancer." | 1.40 | Efficacy of sorafenib and impact on cardiac function in patients with thyroid cancer: a retrospective analysis. ( Giusti, M; Minuto, F; Monti, E; Morbelli, S; Mortara, L; Pera, G; Sambuceti, G, 2014) |
"Sorafenib has proven efficacy in advanced differentiated thyroid cancer (DTC), but many patients must reduce the dose or discontinue treatment because of toxicity." | 1.40 | Efficacy and tolerability of different starting doses of sorafenib in patients with differentiated thyroid cancer. ( Bassett, RL; Busaidy, NL; Cabanillas, ME; Dadu, R; Habra, MA; Hu, MI; Jimenez, C; Sherman, SI; Waguespack, SG; Ying, AK, 2014) |
"Thyroid cancer is the most prevalent endocrine malignancy." | 1.40 | To treat or not to treat: developments in the field of advanced differentiated thyroid cancer. ( Corssmit, EP; Kapiteijn, E; Links, TP; Oosting, SF; Schneider, TC; van der Horst-Schrivers, AN, 2014) |
"Sorafenib was mostly well tolerated, but a high incidence of fatal events was reported (three patients died from severe bleeding events and two from cardiac arrest)." | 1.39 | Sorafenib in advanced iodine-refractory differentiated thyroid cancer: efficacy, safety and exploratory analysis of role of serum thyroglobulin and FDG-PET. ( Camera, L; Colao, A; Del Prete, M; Esposito, R; Faggiano, A; Fonti, R; Marotta, V; Palmieri, G; Ramundo, V; Salvatore, M; Vitale, M, 2013) |
"Medullary thyroid cancer (MTC) is frequently associated with mutations in the tyrosine kinase Ret and with increased expression of vascular endothelial growth factor (VEGF) and VEGF receptor 2 (VEGFR2)." | 1.38 | Anti-tumor activity of motesanib in a medullary thyroid cancer model. ( Bready, J; Canon, J; Coxon, A; Estrada, J; Hughes, P; Kaufman, S; Kendall, R; Osgood, T; Polverino, A; Radinsky, R; Wang, L, 2012) |
"Everolimus was neither additive nor syngergistic in combination with sorafenib or AZD6244." | 1.38 | Sorafenib and Mek inhibition is synergistic in medullary thyroid carcinoma in vitro. ( Agarwal, K; Brendel, VJ; Jarjoura, D; Koh, YW; Koo, BS; McCarty, SK; Porter, K; Ringel, MD; Saji, M; Shah, MH; Wang, C, 2012) |
"Although thyroid cancer usually has an excellent prognosis, few therapeutic options are available in the refractory setting." | 1.38 | Sorafenib in metastatic thyroid cancer. ( Capdevila, J; Corral, J; Grande, E; Grau, JJ; Halperin, I; Iglesias, L; Martínez-Trufero, J; Obiols, G; Segura, A; Tabernero, J; Vaz, MÁ, 2012) |
"Here we present a man with pancreatic metastases from PTC, report our experience with sorafenib therapy, and discuss the role of endoscopic ultrasound (EUS)-guided biopsy in its diagnosis." | 1.38 | Pancreatic metastasis arising from a BRAF(V600E)-positive papillary thyroid cancer: the role of endoscopic ultrasound-guided biopsy and response to sorafenib therapy. ( Abalkhail, H; Al Sohaibani, F; Almanea, H; AlQaraawi, A; Alzahrani, AS, 2012) |
"Sorafenib has shown promise in the treatment of patients with advanced or metastatic thyroid carcinoma." | 1.38 | Brain metastasis from follicular thyroid carcinoma: treatment with sorafenib. ( Chen, L; Lu, H; Luo, Q; Ruan, M; Shen, Y; Yu, Y; Zhu, R, 2012) |
"Medullary thyroid cancer-1." | 1.38 | Autophagic activation potentiates the antiproliferative effects of tyrosine kinase inhibitors in medullary thyroid cancer. ( Lin, CI; Lorch, JH; Ruan, DT; Whang, EE, 2012) |
" The mice were randomized into seven groups: blank control (A), vehicle control (B), single liposome doxorubicin (C), single sorafenib group (D), liposome doxorubicin combined with low dose sorafenib group (E), combined group with medium dosage of sorafenib (F), combined group with high-dose of sorafenib(G)." | 1.38 | [Effects of sorafenib and liposome doxorubicin on human poorly differentiated thyroid carcinoma xenografts in nude mice]. ( An, CM; Han, ZK; Li, ZJ; Ma, J; Tang, PZ; Wang, Z, 2012) |
"Patients with progressive refractory thyroid cancer are potential candidates for clinical trials using tyrosine kinase inhibitors (TKIs), and a promising proportion of patients in these trials have achieved stable disease." | 1.37 | Fatal heart failure after a 26-month combination of tyrosine kinase inhibitors in a papillary thyroid cancer. ( Bousquet, G; Faugeron, I; Hindie, E; Lussato, D; Toubert, ME; Vercellino, L, 2011) |
" 3 patients remain on sorafenib, 2 at a reduced dosage (600 mg/d)." | 1.37 | Rapid response to sorafenib in metastatic medullary thyroid carcinoma. ( Frank-Raue, K; Ganten, M; Kreissl, MC; Raue, F, 2011) |
"Sorafenib is a multikinase inhibitor that blocks tumor cell proliferation and angiogenesis and is used for the treatment of advanced renal cell carcinoma, unresectable hepatocellular carcinoma, and other solid tumors." | 1.36 | Sorafenib-induced psoriasiform eruption in a patient with metastatic thyroid carcinoma. ( Chon, SY; Diamantis, ML, 2010) |
"Sorafenib was used in 13 and sunitinib in two, including one patient who failed prior sorafenib therapy." | 1.36 | Treatment with tyrosine kinase inhibitors for patients with differentiated thyroid cancer: the M. D. Anderson experience. ( Bronstein, Y; Busaidy, NL; Cabanillas, ME; Feng, L; Hernandez, M; Lopez, A; Sherman, SI; Waguespack, SG; Williams, MD, 2010) |
" Dose-response simulations were performed in patients with differentiated thyroid cancer." | 1.36 | Development of a modeling framework to simulate efficacy endpoints for motesanib in patients with thyroid cancer. ( Bruno, R; Claret, L; Lu, JF; Sun, YN, 2010) |
" Motesanib concentrations were fitted to a 2-compartment population pharmacokinetic model." | 1.36 | Population pharmacokinetic/pharmacodynamic modeling for the time course of tumor shrinkage by motesanib in thyroid cancer patients. ( Bruno, R; Claret, L; Kuchimanchi, M; Lu, JF; Melara, R; Sun, YN; Sutjandra, L, 2010) |
"Sorafenib is an orally administered multi-kinase inhibitor that has shown promise in the treatment of adults with advanced thyroid cancer, but it has not yet been studied in children with this disease." | 1.35 | The successful use of sorafenib to treat pediatric papillary thyroid carcinoma. ( Clayman, GL; Herzog, CE; Sherman, SI; Waguespack, SG; Williams, MD, 2009) |
"Suppression of BRAF pathway in thyroid cancer cell lines (8505C, TPC1 and C643) was achieved using RNA interference (RNAi) for BRAF and the kinase inhibitor, sorafenib." | 1.35 | Proliferation and survival molecules implicated in the inhibition of BRAF pathway in thyroid cancer cells harbouring different genetic mutations. ( Figueiredo, J; Gonçalves, J; Meireles, AM; Preto, A; Rebocho, AP; Rocha, AS; Seca, H; Seruca, R; Soares, P; Sobrinho-Simões, M; Vasconcelos, HM, 2009) |
"Differentiated thyroid cancer and hyperthyroidism are treated with radioiodine." | 1.33 | Nicotinamide increases thyroid radiosensitivity by stimulating nitric oxide synthase expression and the generation of organic peroxides. ( Agote Robertson, M; Dagrosa, MA; Finochietto, P; Franco, MC; Gamba, CA; Juvenal, GJ; Pisarev, MA; Poderoso, JJ; Viaggi, ME, 2006) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 1 (0.61) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 22 (13.33) | 29.6817 |
2010's | 138 (83.64) | 24.3611 |
2020's | 4 (2.42) | 2.80 |
Authors | Studies |
---|---|
Farias, EC | 1 |
Hoff, AO | 4 |
Oya, M | 1 |
Kaneko, S | 1 |
Imai, T | 1 |
Tsujino, T | 1 |
Sunaya, T | 1 |
Okayama, Y | 1 |
Celano, M | 1 |
Maggisano, V | 1 |
Bulotta, S | 1 |
Allegri, L | 1 |
Pecce, V | 1 |
Abballe, L | 1 |
Damante, G | 1 |
Russo, D | 1 |
Tang, K | 1 |
Wang, Z | 2 |
Lin, J | 1 |
Zheng, X | 1 |
Wilson, L | 1 |
Huang, W | 1 |
Chen, L | 5 |
Ting, J | 1 |
Cao, V | 1 |
Yi, H | 2 |
Ye, X | 3 |
Long, B | 2 |
Ye, T | 2 |
Zhang, L | 2 |
Yan, F | 1 |
Yang, Y | 1 |
Li, L | 2 |
Ito, Y | 1 |
Onoda, N | 1 |
Ito, KI | 1 |
Sugitani, I | 2 |
Takahashi, S | 1 |
Yamaguchi, I | 1 |
Kabu, K | 1 |
Tsukada, K | 1 |
Sherman, EJ | 1 |
Dunn, LA | 1 |
Ho, AL | 1 |
Baxi, SS | 1 |
Ghossein, RA | 1 |
Fury, MG | 1 |
Haque, S | 1 |
Sima, CS | 1 |
Cullen, G | 1 |
Fagin, JA | 3 |
Pfister, DG | 2 |
Sawa, A | 1 |
Chiba, T | 1 |
Ishii, J | 1 |
Yamamoto, H | 1 |
Hara, H | 1 |
Kamma, H | 1 |
Pacini, F | 3 |
Matrone, A | 1 |
Valerio, L | 1 |
Pieruzzi, L | 1 |
Giani, C | 1 |
Cappagli, V | 1 |
Lorusso, L | 1 |
Agate, L | 1 |
Puleo, L | 1 |
Viola, D | 1 |
Bottici, V | 1 |
Del Re, M | 1 |
Molinaro, E | 1 |
Danesi, R | 1 |
Elisei, R | 3 |
Felicetti, F | 2 |
Nervo, A | 2 |
Piovesan, A | 2 |
Berardelli, R | 1 |
Marchisio, F | 1 |
Gallo, M | 2 |
Arvat, E | 2 |
Ge, M | 1 |
Yang, M | 1 |
Jin, S | 1 |
Molina-Vega, M | 1 |
García-Alemán, J | 1 |
Sebastián-Ochoa, A | 1 |
Mancha-Doblas, I | 1 |
Trigo-Pérez, JM | 1 |
Tinahones-Madueño, F | 1 |
Danilovic, DLS | 1 |
Castro, G | 1 |
Roitberg, FSR | 1 |
Vanderlei, FAB | 1 |
Bonani, FA | 1 |
Freitas, RMC | 1 |
Coura-Filho, GB | 1 |
Camargo, RY | 1 |
Kulcsar, MA | 3 |
Marui, S | 1 |
Iyer, P | 1 |
Mayer, JL | 1 |
Ewig, JM | 1 |
Martínez-Rodríguez, I | 1 |
Banzo, I | 1 |
Carril, JM | 1 |
Kurzrock, R | 3 |
Atkins, J | 1 |
Wheler, J | 2 |
Fu, S | 1 |
Naing, A | 2 |
Busaidy, N | 1 |
Hong, D | 2 |
Sherman, S | 1 |
Shawa, H | 1 |
Busaidy, NL | 5 |
Schellingerhout, D | 1 |
Habra, MA | 3 |
Eisner, F | 1 |
Schaberl-Moser, R | 1 |
Gerger, A | 1 |
Samonigg, H | 1 |
Pichler, M | 1 |
Fallahi, P | 3 |
Ferrari, SM | 3 |
Santini, F | 1 |
Corrado, A | 2 |
Materazzi, G | 3 |
Ulisse, S | 3 |
Miccoli, P | 3 |
Antonelli, A | 3 |
Wunderlich, A | 1 |
Khoruzhyk, M | 1 |
Roth, S | 1 |
Ramaswamy, A | 1 |
Greene, BH | 1 |
Doll, D | 1 |
Bartsch, DK | 1 |
Hoffmann, S | 1 |
Owonikoko, TK | 1 |
Chowdry, RP | 1 |
Chen, Z | 1 |
Kim, S | 3 |
Saba, NF | 1 |
Shin, DM | 1 |
Khuri, FR | 1 |
Shen, CT | 2 |
Qiu, ZL | 2 |
Luo, QY | 2 |
Hescot, S | 1 |
Baudin, E | 2 |
Borson-Chazot, F | 1 |
Lombès, M | 1 |
Bellesoeur, A | 2 |
Carton, E | 1 |
Mir, O | 2 |
Groussin, L | 1 |
Blanchet, B | 3 |
Billemont, B | 1 |
Clerc, J | 2 |
Goldwasser, F | 5 |
Massicotte, MH | 1 |
Brassard, M | 1 |
Claude-Desroches, M | 1 |
Borget, I | 1 |
Bonichon, F | 2 |
Giraudet, AL | 1 |
Do Cao, C | 1 |
Chougnet, CN | 1 |
Leboulleux, S | 1 |
Schlumberger, M | 5 |
de la Fouchardière, C | 4 |
Barroso-Sousa, R | 1 |
Lerario, AM | 1 |
Evangelista, J | 1 |
Papadia, C | 2 |
Lourenço, DM | 1 |
Lin, CS | 1 |
Fragoso, MC | 1 |
Thomas, L | 1 |
Lai, SY | 2 |
Dong, W | 1 |
Feng, L | 2 |
Dadu, R | 4 |
Regone, RM | 1 |
Cabanillas, ME | 6 |
Devine, C | 1 |
Hernandez, M | 3 |
Waguespack, SG | 6 |
Hu, MI | 2 |
Jimenez, C | 2 |
Sellin, RV | 1 |
Ying, AK | 2 |
Cote, GJ | 1 |
Sherman, SI | 13 |
Liu, M | 2 |
Shen, Y | 3 |
Ruan, M | 3 |
Li, M | 1 |
Pitoia, F | 4 |
Bassett, RL | 1 |
Haraldsdottir, S | 1 |
Shah, MH | 6 |
Brose, MS | 8 |
Nutting, CM | 3 |
Jarzab, B | 4 |
Siena, S | 2 |
Bastholt, L | 3 |
Paschke, R | 1 |
Shong, YK | 3 |
Smit, JW | 7 |
Chung, J | 3 |
Kappeler, C | 4 |
Peña, C | 2 |
Molnár, I | 1 |
Schlumberger, MJ | 5 |
Galli, F | 1 |
Manni, I | 1 |
Piaggio, G | 1 |
Balogh, L | 1 |
Weintraub, BD | 1 |
Szkudlinski, MW | 1 |
Fremont, V | 1 |
Dierckx, RA | 1 |
Signore, A | 1 |
Takami, H | 1 |
Ito, K | 1 |
Sugino, K | 1 |
Huillard, O | 2 |
Boudou-Rouquette, P | 2 |
Thomas-Schoemann, A | 2 |
Wassermann, J | 1 |
Marotta, V | 4 |
Sciammarella, C | 2 |
Vitale, M | 2 |
Colao, A | 4 |
Faggiano, A | 4 |
Mortara, L | 1 |
Pera, G | 1 |
Monti, E | 1 |
Morbelli, S | 1 |
Minuto, F | 1 |
Sambuceti, G | 1 |
Giusti, M | 1 |
Di Somma, C | 1 |
Rubino, M | 1 |
Modica, R | 1 |
Camera, L | 2 |
Del Prete, M | 2 |
Marciello, F | 1 |
Ramundo, V | 2 |
Circelli, L | 1 |
Buonomano, P | 1 |
Schneider, TC | 3 |
Kapiteijn, E | 5 |
Corssmit, EP | 4 |
Oosting, SF | 1 |
van der Horst-Schrivers, AN | 1 |
Links, TP | 1 |
Michelon, F | 1 |
Castiglione, A | 1 |
Viansone, AA | 1 |
Zichi, C | 1 |
Ciccone, G | 1 |
Lindner, C | 1 |
Dierneder, J | 1 |
Pall, G | 1 |
Pirich, C | 1 |
Hoffmann, M | 1 |
Raderer, M | 1 |
Becherer, A | 1 |
Niederle, B | 1 |
Lipp, R | 1 |
Lind, P | 1 |
Gallowitsch, H | 1 |
Romeder, F | 1 |
Virgolini, I | 1 |
Tuttle, RM | 2 |
Haddad, RI | 1 |
Ball, DW | 1 |
Byrd, D | 1 |
Dickson, P | 1 |
Duh, QY | 1 |
Ehya, H | 1 |
Haymart, M | 1 |
Hoh, C | 1 |
Hunt, JP | 1 |
Iagaru, A | 1 |
Kandeel, F | 1 |
Kopp, P | 1 |
Lamonica, DM | 1 |
Lydiatt, WM | 1 |
McCaffrey, J | 1 |
Moley, JF | 2 |
Parks, L | 1 |
Raeburn, CD | 1 |
Ridge, JA | 1 |
Ringel, MD | 4 |
Scheri, RP | 1 |
Shah, JP | 1 |
Sturgeon, C | 1 |
Wang, TN | 1 |
Wirth, LJ | 4 |
Hoffmann, KG | 1 |
Hughes, M | 1 |
Krajewska, J | 2 |
Handkiewicz-Junak, D | 1 |
Gruber, JJ | 1 |
Colevas, AD | 1 |
Mato, E | 1 |
Barceló-Batllori, S | 1 |
Orera, I | 1 |
Selva, L | 1 |
Corra, M | 1 |
González, C | 1 |
Bell, O | 1 |
Lerma, E | 1 |
Moral, A | 1 |
Pérez, JI | 1 |
de Leiva, A | 1 |
White, PT | 1 |
Cohen, MS | 2 |
Chen, G | 1 |
Nicula, D | 1 |
Renko, K | 1 |
Derwahl, M | 1 |
Durand, JP | 1 |
Lee, HJ | 1 |
Ryu, H | 1 |
Choi, YS | 1 |
Song, IC | 1 |
Yun, HJ | 1 |
Jo, DY | 1 |
Blair, HA | 1 |
Plosker, GL | 1 |
Dong, Q | 1 |
Broecker-Preuss, M | 1 |
Müller, S | 1 |
Britten, M | 1 |
Worm, K | 1 |
Schmid, KW | 1 |
Mann, K | 1 |
Fuhrer, D | 1 |
Wang, E | 1 |
Karedan, T | 1 |
Perez, CA | 2 |
Moreo, A | 1 |
Vallerio, P | 1 |
Ricotta, R | 1 |
Stucchi, M | 1 |
Pozzi, M | 1 |
Musca, F | 1 |
Meani, P | 1 |
Maloberti, A | 1 |
Facchetti, R | 1 |
Di Bella, S | 1 |
Giganti, MO | 1 |
Sartore-Bianchi, A | 1 |
Mancia, G | 1 |
Giannattasio, C | 1 |
Carneiro, RM | 1 |
Carneiro, BA | 1 |
Agulnik, M | 1 |
Kopp, PA | 1 |
Giles, FJ | 1 |
Politti, U | 2 |
Mazzi, V | 1 |
Miccoli, M | 1 |
Spisni, R | 1 |
Baldini, E | 1 |
Gadaleta-Caldarola, G | 1 |
Infusino, S | 1 |
Divella, R | 1 |
Ferraro, E | 1 |
Mazzocca, A | 1 |
De Rose, F | 1 |
Filippelli, G | 1 |
Abbate, I | 1 |
Brandi, M | 1 |
Martin del Campo, SE | 1 |
Levine, KM | 1 |
Mundy-Bosse, BL | 1 |
Grignol, VP | 1 |
Fairchild, ET | 1 |
Campbell, AR | 1 |
Trikha, P | 1 |
Mace, TA | 1 |
Paul, BK | 1 |
Jaime-Ramirez, AC | 1 |
Markowitz, J | 1 |
Kondadasula, SV | 1 |
Guenterberg, KD | 1 |
McClory, S | 1 |
Karpa, VI | 1 |
Pan, X | 1 |
Olencki, TE | 1 |
Monk, JP | 1 |
Mortazavi, A | 1 |
Tridandapani, S | 1 |
Lesinski, GB | 1 |
Byrd, JC | 1 |
Caligiuri, MA | 1 |
Carson, WE | 1 |
Kiyota, N | 1 |
Zhang, J | 1 |
Yu, J | 1 |
Xie, R | 1 |
Chen, W | 1 |
Lv, Y | 1 |
Abelleira, E | 1 |
Jerkovich, F | 2 |
Urciuoli, C | 1 |
Cross, G | 1 |
Covell, LL | 1 |
Ganti, AK | 1 |
Hammami, MM | 1 |
Duaiji, N | 1 |
Mutairi, G | 1 |
Aklabi, S | 1 |
Qattan, N | 1 |
Abouzied, Mel-D | 1 |
Sous, MW | 1 |
Worden, F | 1 |
Fassnacht, M | 2 |
Shi, Y | 1 |
Hadjieva, T | 1 |
Gao, M | 1 |
Fugazzola, L | 1 |
Ando, Y | 1 |
Hasegawa, Y | 1 |
Park, DJ | 1 |
Meinhardt, G | 1 |
Zhu, Y | 1 |
Cai, J | 1 |
Dunna, NR | 1 |
Kandula, V | 1 |
Girdhar, A | 1 |
Pudutha, A | 1 |
Hussain, T | 1 |
Bandaru, S | 1 |
Nayarisseri, A | 1 |
de Castroneves, LA | 1 |
Negrão, MV | 1 |
de Freitas, RM | 1 |
Lima, JV | 1 |
Fukushima, JT | 1 |
Simão, EF | 1 |
Tavares, MR | 1 |
Jorge, AA | 1 |
de Castro, G | 1 |
Hoff, PM | 1 |
Fiskus, W | 1 |
Mitsiades, N | 1 |
van Wezel, T | 1 |
Smit, JWA | 1 |
van der Hoeven, JJM | 1 |
Morreau, H | 3 |
Jean, GW | 1 |
Mani, RM | 1 |
Jaffry, A | 1 |
Khan, SA | 1 |
Okano, S | 1 |
Yarchoan, M | 1 |
Ma, C | 1 |
Troxel, AB | 2 |
Stopenski, SJ | 1 |
Tang, W | 1 |
Cohen, AB | 1 |
Pappas-Paxinos, M | 1 |
Johnson, BA | 1 |
Chen, EY | 1 |
Feldman, MD | 1 |
Mirantes, C | 1 |
Dosil, MA | 1 |
Eritja, N | 1 |
Felip, I | 1 |
Gatius, S | 1 |
Santacana, M | 1 |
Matias-Guiu, X | 1 |
Dolcet, X | 1 |
Abdulghani, J | 1 |
Gokare, P | 1 |
Gallant, JN | 1 |
Dicker, D | 1 |
Whitcomb, T | 1 |
Cooper, T | 1 |
Liao, J | 1 |
Derr, J | 1 |
Liu, J | 1 |
Goldenberg, D | 1 |
Finnberg, NK | 1 |
El-Deiry, WS | 1 |
Kukulska, A | 1 |
Basu, S | 1 |
Joshi, A | 1 |
Kawalec, P | 1 |
Malinowska-Lipień, I | 1 |
Brzostek, T | 1 |
Kózka, M | 1 |
Dang, RP | 1 |
McFarland, D | 1 |
Le, VH | 1 |
Camille, N | 1 |
Miles, BA | 1 |
Teng, MS | 1 |
Genden, EM | 1 |
Misiukiewicz, KJ | 1 |
Smit, J | 1 |
Lin, CC | 1 |
Fellous, M | 1 |
DeSanctis, Y | 1 |
Tori, M | 1 |
Gupta-Abramson, V | 1 |
Nellore, A | 1 |
Puttaswamy, K | 1 |
Redlinger, M | 1 |
Ransone, K | 1 |
Mandel, SJ | 1 |
Flaherty, KT | 1 |
Loevner, LA | 1 |
O'Dwyer, PJ | 1 |
Droz, JP | 2 |
Hofmann, M | 1 |
Martins, RG | 2 |
Licitra, L | 1 |
Eschenberg, MJ | 2 |
Sun, YN | 4 |
Juan, T | 2 |
Stepan, DE | 2 |
Stenner, F | 1 |
Liewen, H | 1 |
Zweifel, M | 1 |
Weber, A | 1 |
Tchinda, J | 1 |
Bode, B | 1 |
Samaras, P | 1 |
Bauer, S | 1 |
Knuth, A | 1 |
Renner, C | 1 |
Henderson, YC | 1 |
Ahn, SH | 1 |
Kang, Y | 1 |
Clayman, GL | 2 |
Schramm, C | 1 |
Schuch, G | 1 |
Lohse, AW | 1 |
Diaz-Cano, SJ | 1 |
Kloos, RT | 2 |
Knopp, MV | 2 |
Hall, NC | 2 |
King, M | 1 |
Stevens, R | 1 |
Liang, J | 2 |
Wakely, PE | 2 |
Vasko, VV | 2 |
Saji, M | 3 |
Rittenberry, J | 1 |
Wei, L | 2 |
Arbogast, D | 2 |
Collamore, M | 2 |
Wright, JJ | 3 |
Grever, M | 1 |
Williams, MD | 2 |
Herzog, CE | 1 |
Nucera, C | 1 |
Goldfarb, M | 1 |
Hodin, R | 1 |
Parangi, S | 1 |
Locati, LD | 1 |
Daumerie, C | 1 |
Spector, E | 1 |
Franklin, MJ | 1 |
Truskinovsky, AM | 1 |
Dudek, AZ | 1 |
Hoftijzer, H | 2 |
Heemstra, KA | 1 |
Stokkel, MP | 1 |
Gelderblom, H | 2 |
Weijers, K | 1 |
Pereira, AM | 2 |
Huijberts, M | 1 |
Romijn, JA | 2 |
Preto, A | 1 |
Gonçalves, J | 1 |
Rebocho, AP | 1 |
Figueiredo, J | 1 |
Meireles, AM | 1 |
Rocha, AS | 1 |
Vasconcelos, HM | 1 |
Seca, H | 1 |
Seruca, R | 1 |
Soares, P | 2 |
Sobrinho-Simões, M | 2 |
Alfano, RW | 1 |
Leppla, SH | 1 |
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Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
A Phase 1 Dose-Escalation Study of the Safety and Pharmacokinetics of XL184 Administered Orally to Subjects With Advanced Malignancies[NCT00215605] | Phase 1 | 85 participants (Actual) | Interventional | 2005-09-30 | Completed | ||
Phase I Study of Tipifarnib (R115777) and Sorafenib (BAY 43-9006) in Patients With Biopsiable Advanced Cancers[NCT00244972] | Phase 1 | 74 participants (Actual) | Interventional | 2005-10-31 | Completed | ||
A Phase I/Ib, Multicenter, Open-Label, Dose Escalation Study of E7080 in Patients With Solid Tumors and in Combination With Temozolomide in Patients With Advanced and/or Metastatic Melanoma[NCT00121680] | Phase 1 | 115 participants (Actual) | Interventional | 2005-07-31 | Completed | ||
A Multi-Arm Complete Phase 1 Trial of Valproic Acid-Based 2-Agent Oral Regimens for Patients With Advanced Solid Tumor[NCT00495872] | Phase 1 | 204 participants (Actual) | Interventional | 2007-06-30 | Completed | ||
Vessels Encapsulating Tumor Clusters (VETC), Prognostic and Predictive Value in Renal Cell Carcinoma and Adrenal Gland Carcinoma[NCT04666220] | 180 participants (Anticipated) | Observational | 2021-01-02 | Recruiting | |||
A Double-Blind Randomized Phase III Study Evaluating the Efficacy and Safety of Sorafenib Compared to Placebo in Locally Advanced/Metastatic RAI-Refractory Differentiated Thyroid Cancer[NCT00984282] | Phase 3 | 417 participants (Actual) | Interventional | 2009-10-15 | Completed | ||
RIFTOS MKI - Radioactive Iodine reFractory Asymptomatic Patients in Differentiated Thyroid Cancer - an Observational Study to Assess the Use of Multikinase Inhibitors[NCT02303444] | 667 participants (Actual) | Observational | 2015-04-08 | Completed | |||
Impact of BRAFV600E Intratumor Heterogeneity on the Efficacy of Tyrosine Kinase Inhibitors in the Treatment of Radioiodine-resistant Thyroid Cancer[NCT01700699] | 50 participants (Anticipated) | Observational | 2012-10-31 | Recruiting | |||
A Randomized, Multicenter, Open-label, Phase II Study of the Optimal Scheme of Administration of Pazopanib in Thyroid Carcinoma[NCT01813136] | Phase 2 | 168 participants (Actual) | Interventional | 2013-03-31 | Completed | ||
A Phase 2, Open-label Study of AMG 706 to Treat Subjects With Locally Advanced or Metastatic Thyroid Cancer[NCT00121628] | Phase 2 | 184 participants (Actual) | Interventional | 2005-07-31 | Completed | ||
Personalized Cancer Therapy for Patients With Metastatic Medullary Thyroid or Metastatic Colon Cancer[NCT02363647] | 10 participants (Actual) | Interventional | 2015-01-31 | Terminated (stopped due to No Current Funding) | |||
Sorafenib as Adjuvant to Radioiodine Therapy in Non-Medullary Thyroid Carcinoma[NCT00887107] | Phase 2 | 32 participants (Actual) | Interventional | 2007-10-31 | Completed | ||
Analyzing the Patterns of Patient Engagement and Trends in Participation Observed in Medullary Thyroid Cancer Clinical Trials[NCT06079723] | 500 participants (Anticipated) | Observational | 2024-11-30 | Not yet recruiting | |||
Phase II Trial of BAY 43-9006 in Patients With Advanced Anaplastic Carcinoma of the Thyroid[NCT00126568] | Phase 2 | 20 participants (Actual) | Interventional | 2005-06-30 | Terminated | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
Sorafenib AUC(0-12h),ss (area under the concentration time curve from time 0 to 12 hours at steady state) was estimated from the steady state plasma concentration. (NCT00984282)
Timeframe: A single pharmacokinetic plasma sample was collected at steady state (after 14 days of uninterrupted, unmodified sorafenib dosing)
Intervention | mg*h/L (Geometric Mean) |
---|---|
Sorafenib (Nexavar, BAY43-9006) | 75.4 |
Disease control rate was defined as the proportion of subjects whose best response was complete response (CR), partial response (PR), or stable disease (SD). Per Response Evaluation Criteria in Solid Tumors (RECIST) criteria, CR and PR were to be confirmed by another scan at least 4 weeks later; SD had to be documented at least 4 weeks after date of randomization. CR = Disappearance of all clinical and radiological evidence of tumor (both target and no-target). PR = At least a 30% decrease in the sum of LD of target lesions taking as reference the baseline sum. SD = steady state of disease which is neither sufficient shrinkage to qualify for PR nor sufficient increase to qualify for PD. (NCT00984282)
Timeframe: From randomization of the first subject until the database cut-off (31 Aug 2012), study duration approximately three years
Intervention | Percentage of participants (Number) |
---|---|
Sorafenib (Nexavar, BAY43-9006) | 86.2 |
Placebo | 74.6 |
Duration of response was defined as the time from the first documented objective response of PR or CR, whichever was noted earlier, to disease progression or death (if death occurred before progression was documented). CR = Disappearance of all clinical and radiological evidence of tumor (both target and no-target). PR = At least a 30% decrease in the sum of LD of target lesions taking as reference the baseline sum. (NCT00984282)
Timeframe: From randomization of the first subject until the database cut-off (31 Aug 2012), study duration approximately three years
Intervention | Days (Median) |
---|---|
Sorafenib (Nexavar, BAY43-9006) | 309 |
Placebo | NA |
Overall survival was defined as the time (days) from date of randomization to date of death due to any cause. Subjects still alive at the time of analysis were censored at their date of last contact. Since the median value could not be estimated due to censored data, the percentage of participants who died is presented. (NCT00984282)
Timeframe: From randomization of the first subject until the database cut-off (30 AUG 2017), study duration approximately eight years
Intervention | Percentage of participants (Number) |
---|---|
Sorafenib (Nexavar, BAY43-9006) | 52.7 |
Placebo | 54.8 |
PFS=time from randomization to first observed disease progression (radiological according to central assessment or clinical due to bone irradiation, whichever is earlier), or death due to any cause, if death occurred before progression. Progression was assessed by RECIST criteria, version 1.0, modified for bone lesions. PFS for participants without disease progression or death at the time of analysis or unblinding were censored at the last date of tumor assessment before unblinding. Participants with no tumor evaluation after baseline were censored at Day 1. PD (Progression Disease)=At least a 20% increase in sum of longest diameters (LD) of measured lesions taking as reference the smallest sum LD on study since the treatment started or the appearance of 1 or more new lesions. New lesions also constituted PD. In exceptional circumstances, unequivocal progression of a nonmeasured lesion may have been accepted as evidence of disease progression in participants with measurable disease. (NCT00984282)
Timeframe: Final analysis to be performed when approximately 267 progression-free survival events (centrally assessed) had occurred, study duration approximately three years
Intervention | Days (Median) |
---|---|
Sorafenib (Nexavar, BAY43-9006) | 329 |
Placebo | 175 |
Response rate was defined as the proportion of subjects whose best response was CR or PR. Per RECIST, CR and PR was to be confirmed by another scan at least 4 weeks later. CR = Disappearance of all clinical and radiological evidence of tumor (both target and no-target). PR = At least a 30% decrease in the sum of LD of target lesions taking as reference the baseline sum. (NCT00984282)
Timeframe: From randomization of the first subject until the database cut-off (31 Aug 2012), study duration approximately three years
Intervention | Percentage of participants (Number) |
---|---|
Sorafenib (Nexavar, BAY43-9006) | 12.24 |
Placebo | 0.5 |
Time to progression was defined at the time (days) from randomization to progression (based on central assessment [radiological and clinical progression due to bone irradiation]) (NCT00984282)
Timeframe: From randomization of the first subject until the database cut-off (31 Aug 2012), study duration approximately three years
Intervention | Days (Median) |
---|---|
Sorafenib (Nexavar, BAY43-9006) | 337 |
Placebo | 175 |
The magnitude of change from baseline in target lesion size in evaluable participants with scans was determined. (NCT00984282)
Timeframe: From randomization of the first subject until the database cut-off (31 Aug 2012), study duration approximately three years
Intervention | Percentage of participants (Number) | |||||
---|---|---|---|---|---|---|
Reduction ≥ 30% | Reduction ≥ 20% but < 30% | Reduction ≥ 10% but < 20% | Reduction > 0% but < 10% | Growth ≥ 0% | Not assessed | |
Placebo | 1.0 | 1.5 | 3.5 | 21.9 | 62.7 | 9.5 |
Sorafenib (Nexavar, BAY43-9006) | 17.3 | 15.3 | 22.4 | 22.4 | 12.8 | 9.7 |
The safety and toxicity profile of BAY 43-9006 as measured by toxicity grades of adverse events. (NCT00126568)
Timeframe: 27 months
Intervention | Participants (Count of Participants) |
---|---|
Treatment (Sorafenib Tosylate) | 20 |
(NCT00126568)
Timeframe: 27 months
Intervention | months (Median) |
---|---|
BAY 43-9006 | 3.9 |
(NCT00126568)
Timeframe: 27 months
Intervention | months (Median) |
---|---|
BAY 43-9006 | 1.9 |
Response evaluated using the Response Evaluation Criteria in Solid Tumors (RECIST) Committee. The patient's best response depends on the achievement of measurement and confirmation criteria of Complete Response (CR), Stable Disease (SD), Partial Response (PR) or Progressive Disease (PD). Measurable 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. (NCT00126568)
Timeframe: at 6 months after treatment
Intervention | participants (Number) | ||
---|---|---|---|
Partial Response | Stable Disease | Progressive Disease | |
BAY 43-9006 | 2 | 5 | 11 |
37 reviews available for niacinamide and Thyroid Neoplasms
Article | Year |
---|---|
Which patient with thyroid cancer deserves systemic therapy and when?
Topics: Antineoplastic Agents; Humans; Iodine Radioisotopes; Niacinamide; Patient Selection; Phenylurea Comp | 2017 |
Protein kinase inhibitors for the treatment of advanced and progressive radiorefractory thyroid tumors: From the clinical trials to the real life.
Topics: Antineoplastic Agents; Chemotherapy, Adjuvant; Clinical Trials as Topic; Humans; Iodine Radioisotope | 2017 |
Tyrosine kinase inhibitors rechallenge in solid tumors: a review of literature and a case description with lenvatinib in thyroid cancer.
Topics: Adult; Antineoplastic Agents; Disease Progression; Female; Humans; Niacinamide; Phenylurea Compounds | 2017 |
Sorafenib and thyroid cancer.
Topics: Angiogenesis Inhibitors; Animals; Antineoplastic Agents; Carcinoma; Carcinoma, Neuroendocrine; Carci | 2013 |
Sorafenib in the treatment of radioiodine-refractory differentiated thyroid cancer: a meta-analysis.
Topics: Antineoplastic Agents; Drug Resistance, Neoplasm; Humans; Iodine Radioisotopes; Niacinamide; Phenylu | 2014 |
[Targeted therapies, prognostic and predictive factors in endocrine oncology].
Topics: Antineoplastic Agents; Carcinoma, Neuroendocrine; Clinical Trials, Phase III as Topic; Disease-Free | 2013 |
Sorafenib in metastatic thyroid cancer: a systematic review.
Topics: Antineoplastic Agents; Clinical Trials, Phase II as Topic; Disease Progression; Female; Humans; Male | 2014 |
Development of molecular targeted drugs for advanced thyroid cancer in Japan.
Topics: Antineoplastic Agents; Clinical Trials as Topic; Humans; Japan; Molecular Targeted Therapy; Neovascu | 2014 |
Sorafenib (Nexavar) for thyroid cancer.
Topics: Animals; Antineoplastic Agents; Dermatitis, Exfoliative; Humans; Niacinamide; Phenylurea Compounds; | 2014 |
The evolving field of kinase inhibitors in thyroid cancer.
Topics: Angiogenesis Inhibitors; Anilides; Antineoplastic Agents; Humans; Niacinamide; Phenylurea Compounds; | 2015 |
Sorafenib for the treatment of thyroid cancer: an updated review.
Topics: Antineoplastic Agents; Disease-Free Survival; Humans; Iodine Radioisotopes; Niacinamide; Phenylurea | 2015 |
Differentiated thyroid cancer: focus on emerging treatments for radioactive iodine-refractory patients.
Topics: Disease-Free Survival; Humans; Indoles; Iodine Radioisotopes; MAP Kinase Kinase Kinase 1; Niacinamid | 2015 |
The discovery and development of sorafenib for the treatment of thyroid cancer.
Topics: Animals; Antineoplastic Agents; Disease-Free Survival; Drug Approval; Drug Design; Humans; Molecular | 2015 |
Sorafenib: a review of its use in patients with radioactive iodine-refractory, metastatic differentiated thyroid carcinoma.
Topics: Antineoplastic Agents; Humans; Niacinamide; Phenylurea Compounds; Sorafenib; Thyroid Neoplasms | 2015 |
New insights in the treatment of radioiodine refractory differentiated thyroid carcinomas: to lenvatinib and beyond.
Topics: Antineoplastic Agents; Clinical Trials, Phase II as Topic; Humans; Iodine Radioisotopes; Mutation; N | 2015 |
Targeted therapies in advanced differentiated thyroid cancer.
Topics: Antineoplastic Agents; Humans; Molecular Targeted Therapy; Neoplasm Staging; Niacinamide; Outcome As | 2015 |
Aggressive thyroid cancer: targeted therapy with sorafenib.
Topics: Angiogenesis Inhibitors; Antineoplastic Agents; Humans; Neoplasm Metastasis; Niacinamide; Phenylurea | 2017 |
Sorafenib: 10 years after the first pivotal trial.
Topics: Antineoplastic Agents; Carcinoma, Hepatocellular; Carcinoma, Renal Cell; Humans; Liver Neoplasms; Ni | 2015 |
Treatment of advanced thyroid cancer: role of molecularly targeted therapies.
Topics: Anilides; Antineoplastic Agents; Axitinib; Carcinoma, Neuroendocrine; DNA Mutational Analysis; Drug | 2015 |
Relationship between toxicities and clinical benefits of newly approved tyrosine kinase inhibitors in thyroid cancer: A meta-analysis of literature.
Topics: Antineoplastic Agents; Female; Humans; Male; Neoplasm Recurrence, Local; Niacinamide; Odds Ratio; Ph | 2015 |
Targeted treatments of radio-iodine refractory differentiated thyroid cancer.
Topics: Antineoplastic Agents; Clinical Trials as Topic; Humans; Iodine Radioisotopes; Niacinamide; Phenylur | 2015 |
Toxic Effects of Sorafenib in Patients With Differentiated Thyroid Carcinoma Compared With Other Cancers.
Topics: Antineoplastic Agents; Carcinoma; Humans; Neoplasms; Niacinamide; Phenylurea Compounds; Sorafenib; T | 2016 |
[New molecular target therapy for thyroid neoplasms and malignant melanomas].
Topics: Antibodies, Monoclonal; Antineoplastic Agents; Clinical Trials as Topic; Humans; Indoles; Ipilimumab | 2015 |
Selective use of sorafenib in the treatment of thyroid cancer.
Topics: Antineoplastic Agents; Cell Proliferation; Humans; Niacinamide; Phenylurea Compounds; Sorafenib; Thy | 2016 |
Lenvatinib for the treatment of radioiodine-refractory differentiated thyroid carcinoma: a systematic review and indirect comparison with sorafenib.
Topics: Antineoplastic Agents; Humans; Neoplasm Staging; Niacinamide; Phenylurea Compounds; Protein Kinase I | 2016 |
Neoadjuvant Therapy in Differentiated Thyroid Cancer.
Topics: Adenocarcinoma; Antibiotics, Antineoplastic; Antineoplastic Agents; Clinical Trials as Topic; Doxoru | 2016 |
Role of B-Raf(V600E) in differentiated thyroid cancer and preclinical validation of compounds against B-Raf(V600E).
Topics: Benzenesulfonates; Biopsy, Needle; Humans; Isoquinolines; Mutation; Niacinamide; Phenylurea Compound | 2009 |
Tyrosine kinase inhibitors and the thyroid.
Topics: Axitinib; Benzenesulfonates; Clinical Trials as Topic; Gefitinib; Humans; Imidazoles; Indazoles; Ind | 2009 |
Targeting vascular endothelial growth factor receptor in thyroid cancer: the intracellular and extracellular implications.
Topics: Angiogenesis Inhibitors; Antineoplastic Agents; Benzenesulfonates; Drug Delivery Systems; Humans; MA | 2010 |
Targeted molecular therapies in thyroid carcinoma.
Topics: Antineoplastic Agents; Axitinib; Benzenesulfonates; Carcinoma, Medullary; Carcinoma, Papillary; Huma | 2009 |
Sorafenib: rays of hope in thyroid cancer.
Topics: Antineoplastic Agents; Benzenesulfonates; Carcinoma, Papillary; Disease-Free Survival; Drug Interact | 2010 |
Current status of molecularly targeted drugs for the treatment of advanced thyroid cancer.
Topics: Anilides; Benzenesulfonates; Disease Progression; Humans; Molecular Targeted Therapy; Niacinamide; P | 2011 |
Novel molecular targeted therapies for refractory thyroid cancer.
Topics: Angiogenesis Inhibitors; Anilides; Antineoplastic Agents; Axitinib; Benzamides; Benzenesulfonates; B | 2012 |
Role of BRAF in thyroid oncogenesis.
Topics: Benzenesulfonates; Cell Transformation, Neoplastic; Genetic Predisposition to Disease; Humans; Mutat | 2011 |
Hypothyroidism during treatment with tyrosine kinase inhibitors.
Topics: Carcinoma, Renal Cell; Dose-Response Relationship, Drug; Gastrointestinal Neoplasms; Humans; Indoles | 2012 |
How thyroid tumors start and why it matters: kinase mutants as targets for solid cancer pharmacotherapy.
Topics: Animals; Antineoplastic Agents; Benzenesulfonates; Carcinoma, Medullary; Carcinoma, Papillary; Human | 2004 |
Early clinical studies of novel therapies for thyroid cancers.
Topics: Angiogenesis Inhibitors; Antineoplastic Agents; Axitinib; Benzamides; Benzenesulfonates; Carcinoma; | 2008 |
22 trials available for niacinamide and Thyroid Neoplasms
Article | Year |
---|---|
Sorafenib in Japanese Patients with Locally Advanced or Metastatic Medullary Thyroid Carcinoma and Anaplastic Thyroid Carcinoma.
Topics: Adult; Alopecia; Antineoplastic Agents; Carcinoma, Neuroendocrine; Diarrhea; Drug Resistance, Neopla | 2017 |
Phase 2 study evaluating the combination of sorafenib and temsirolimus in the treatment of radioactive iodine-refractory thyroid cancer.
Topics: Adenocarcinoma, Follicular; Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Antineoplastic Co | 2017 |
Tumor marker and measurement fluctuations may not reflect treatment efficacy in patients with medullary thyroid carcinoma on long-term RET inhibitor therapy.
Topics: Adult; Aged; Aged, 80 and over; Anilides; Antineoplastic Agents; Biomarkers, Tumor; Calcitonin; Carc | 2013 |
Tumor marker and measurement fluctuations may not reflect treatment efficacy in patients with medullary thyroid carcinoma on long-term RET inhibitor therapy.
Topics: Adult; Aged; Aged, 80 and over; Anilides; Antineoplastic Agents; Biomarkers, Tumor; Calcitonin; Carc | 2013 |
Tumor marker and measurement fluctuations may not reflect treatment efficacy in patients with medullary thyroid carcinoma on long-term RET inhibitor therapy.
Topics: Adult; Aged; Aged, 80 and over; Anilides; Antineoplastic Agents; Biomarkers, Tumor; Calcitonin; Carc | 2013 |
Tumor marker and measurement fluctuations may not reflect treatment efficacy in patients with medullary thyroid carcinoma on long-term RET inhibitor therapy.
Topics: Adult; Aged; Aged, 80 and over; Anilides; Antineoplastic Agents; Biomarkers, Tumor; Calcitonin; Carc | 2013 |
Tumor marker and measurement fluctuations may not reflect treatment efficacy in patients with medullary thyroid carcinoma on long-term RET inhibitor therapy.
Topics: Adult; Aged; Aged, 80 and over; Anilides; Antineoplastic Agents; Biomarkers, Tumor; Calcitonin; Carc | 2013 |
Tumor marker and measurement fluctuations may not reflect treatment efficacy in patients with medullary thyroid carcinoma on long-term RET inhibitor therapy.
Topics: Adult; Aged; Aged, 80 and over; Anilides; Antineoplastic Agents; Biomarkers, Tumor; Calcitonin; Carc | 2013 |
Tumor marker and measurement fluctuations may not reflect treatment efficacy in patients with medullary thyroid carcinoma on long-term RET inhibitor therapy.
Topics: Adult; Aged; Aged, 80 and over; Anilides; Antineoplastic Agents; Biomarkers, Tumor; Calcitonin; Carc | 2013 |
Tumor marker and measurement fluctuations may not reflect treatment efficacy in patients with medullary thyroid carcinoma on long-term RET inhibitor therapy.
Topics: Adult; Aged; Aged, 80 and over; Anilides; Antineoplastic Agents; Biomarkers, Tumor; Calcitonin; Carc | 2013 |
Tumor marker and measurement fluctuations may not reflect treatment efficacy in patients with medullary thyroid carcinoma on long-term RET inhibitor therapy.
Topics: Adult; Aged; Aged, 80 and over; Anilides; Antineoplastic Agents; Biomarkers, Tumor; Calcitonin; Carc | 2013 |
Tumor marker and measurement fluctuations may not reflect treatment efficacy in patients with medullary thyroid carcinoma on long-term RET inhibitor therapy.
Topics: Adult; Aged; Aged, 80 and over; Anilides; Antineoplastic Agents; Biomarkers, Tumor; Calcitonin; Carc | 2013 |
Tumor marker and measurement fluctuations may not reflect treatment efficacy in patients with medullary thyroid carcinoma on long-term RET inhibitor therapy.
Topics: Adult; Aged; Aged, 80 and over; Anilides; Antineoplastic Agents; Biomarkers, Tumor; Calcitonin; Carc | 2013 |
Tumor marker and measurement fluctuations may not reflect treatment efficacy in patients with medullary thyroid carcinoma on long-term RET inhibitor therapy.
Topics: Adult; Aged; Aged, 80 and over; Anilides; Antineoplastic Agents; Biomarkers, Tumor; Calcitonin; Carc | 2013 |
Tumor marker and measurement fluctuations may not reflect treatment efficacy in patients with medullary thyroid carcinoma on long-term RET inhibitor therapy.
Topics: Adult; Aged; Aged, 80 and over; Anilides; Antineoplastic Agents; Biomarkers, Tumor; Calcitonin; Carc | 2013 |
Tumor marker and measurement fluctuations may not reflect treatment efficacy in patients with medullary thyroid carcinoma on long-term RET inhibitor therapy.
Topics: Adult; Aged; Aged, 80 and over; Anilides; Antineoplastic Agents; Biomarkers, Tumor; Calcitonin; Carc | 2013 |
Tumor marker and measurement fluctuations may not reflect treatment efficacy in patients with medullary thyroid carcinoma on long-term RET inhibitor therapy.
Topics: Adult; Aged; Aged, 80 and over; Anilides; Antineoplastic Agents; Biomarkers, Tumor; Calcitonin; Carc | 2013 |
Tumor marker and measurement fluctuations may not reflect treatment efficacy in patients with medullary thyroid carcinoma on long-term RET inhibitor therapy.
Topics: Adult; Aged; Aged, 80 and over; Anilides; Antineoplastic Agents; Biomarkers, Tumor; Calcitonin; Carc | 2013 |
Clinical efficacy of targeted biologic agents as second-line therapy of advanced thyroid cancer.
Topics: Aged; Antineoplastic Combined Chemotherapy Protocols; Carcinoma, Neuroendocrine; Disease-Free Surviv | 2013 |
Sorafenib in radioactive iodine-refractory, locally advanced or metastatic differentiated thyroid cancer: a randomised, double-blind, phase 3 trial.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Double-Blind Method; Female; Humans; Kaplan-M | 2014 |
Sorafenib in radioactive iodine-refractory, locally advanced or metastatic differentiated thyroid cancer: a randomised, double-blind, phase 3 trial.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Double-Blind Method; Female; Humans; Kaplan-M | 2014 |
Sorafenib in radioactive iodine-refractory, locally advanced or metastatic differentiated thyroid cancer: a randomised, double-blind, phase 3 trial.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Double-Blind Method; Female; Humans; Kaplan-M | 2014 |
Sorafenib in radioactive iodine-refractory, locally advanced or metastatic differentiated thyroid cancer: a randomised, double-blind, phase 3 trial.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Double-Blind Method; Female; Humans; Kaplan-M | 2014 |
Safety and tolerability of sorafenib in patients with radioiodine-refractory thyroid cancer.
Topics: Adenocarcinoma, Follicular; Adenoma, Oxyphilic; Aged; Antineoplastic Agents; Carcinoma, Papillary; D | 2015 |
Phase II trial of sorafenib in advanced thyroid cancer.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Benzenesulfonates; Female; Humans; Male; Midd | 2008 |
Phase II trial of sorafenib in advanced thyroid cancer.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Benzenesulfonates; Female; Humans; Male; Midd | 2008 |
Phase II trial of sorafenib in advanced thyroid cancer.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Benzenesulfonates; Female; Humans; Male; Midd | 2008 |
Phase II trial of sorafenib in advanced thyroid cancer.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Benzenesulfonates; Female; Humans; Male; Midd | 2008 |
Motesanib diphosphate in progressive differentiated thyroid cancer.
Topics: Adenocarcinoma, Follicular; Adenoma, Oxyphilic; Adult; Aged; Aged, 80 and over; Antineoplastic Agent | 2008 |
Motesanib diphosphate in progressive differentiated thyroid cancer.
Topics: Adenocarcinoma, Follicular; Adenoma, Oxyphilic; Adult; Aged; Aged, 80 and over; Antineoplastic Agent | 2008 |
Motesanib diphosphate in progressive differentiated thyroid cancer.
Topics: Adenocarcinoma, Follicular; Adenoma, Oxyphilic; Adult; Aged; Aged, 80 and over; Antineoplastic Agent | 2008 |
Motesanib diphosphate in progressive differentiated thyroid cancer.
Topics: Adenocarcinoma, Follicular; Adenoma, Oxyphilic; Adult; Aged; Aged, 80 and over; Antineoplastic Agent | 2008 |
Phase II trial of sorafenib in metastatic thyroid cancer.
Topics: Adenocarcinoma, Papillary; Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Benzenesulfonates; | 2009 |
Phase II study of safety and efficacy of motesanib in patients with progressive or symptomatic, advanced or metastatic medullary thyroid cancer.
Topics: Adult; Aged; Antineoplastic Agents; Carcinoma, Medullary; Female; Humans; Indoles; Male; Middle Aged | 2009 |
Beneficial effects of sorafenib on tumor progression, but not on radioiodine uptake, in patients with differentiated thyroid carcinoma.
Topics: Adenocarcinoma, Follicular; Aged; Aged, 80 and over; Benzenesulfonates; Bone Neoplasms; Disease-Free | 2009 |
Phase II clinical trial of sorafenib in metastatic medullary thyroid cancer.
Topics: Administration, Oral; Adult; Aged; Benzenesulfonates; Biomarkers, Tumor; Carcinoma, Medullary; Disea | 2010 |
Sorafenib-induced hypothyroidism is associated with increased type 3 deiodination.
Topics: Aged; Aged, 80 and over; Benzenesulfonates; Carcinoma; Female; Humans; Hypothyroidism; Male; Middle | 2010 |
Biomarkers as predictors of response to treatment with motesanib in patients with progressive advanced thyroid cancer.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Biomarkers; Carcinoma, Medullary; | 2010 |
Sorafenib: rays of hope in thyroid cancer.
Topics: Antineoplastic Agents; Benzenesulfonates; Carcinoma, Papillary; Disease-Free Survival; Drug Interact | 2010 |
Response to sorafenib at a low dose in patients with radioiodine-refractory pulmonary metastases from papillary thyroid carcinoma.
Topics: Adult; Aged; Antineoplastic Agents; Benzenesulfonates; Carcinoma; Carcinoma, Papillary; China; Disea | 2011 |
Inhibition of the Ras/Raf/MEK/ERK and RET kinase pathways with the combination of the multikinase inhibitor sorafenib and the farnesyltransferase inhibitor tipifarnib in medullary and differentiated thyroid malignancies.
Topics: Adenocarcinoma, Follicular; Adult; Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Pro | 2011 |
In vitro transforming potential, intracellular signaling properties, and sensitivity to a kinase inhibitor (sorafenib) of RET proto-oncogene variants Glu511Lys, Ser649Leu, and Arg886Trp.
Topics: Adult; Aged; Animals; Basic Helix-Loop-Helix Leucine Zipper Transcription Factors; Benzenesulfonates | 2011 |
Analysis of the efficacy and toxicity of sorafenib in thyroid cancer: a phase II study in a UK based population.
Topics: Adult; Aged; Antineoplastic Agents; Benzenesulfonates; Carcinoma; Female; Humans; Male; Middle Aged; | 2011 |
Rationale and design of decision: a double-blind, randomized, placebo-controlled phase III trial evaluating the efficacy and safety of sorafenib in patients with locally advanced or metastatic radioactive iodine (RAI)-refractory, differentiated thyroid ca
Topics: Antineoplastic Agents; Benzenesulfonates; Clinical Protocols; Double-Blind Method; Drug Administrati | 2011 |
Long-term analysis of the efficacy and tolerability of sorafenib in advanced radio-iodine refractory differentiated thyroid carcinoma: final results of a phase II trial.
Topics: Adenocarcinoma, Follicular; Adenoma, Oxyphilic; Aged; Aged, 80 and over; Antineoplastic Agents; Benz | 2012 |
Phase II trial of sorafenib in patients with advanced anaplastic carcinoma of the thyroid.
Topics: Adult; Aged; Antineoplastic Agents; Carcinoma; Drug Eruptions; Drug Resistance, Multiple; Drug Resis | 2013 |
107 other studies available for niacinamide and Thyroid Neoplasms
Article | Year |
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Valuable insights from real-life experiences of advanced thyroid cancer treatment with sorafenib in Latin America.
Topics: Antineoplastic Agents; Humans; Latin America; Niacinamide; Phenylurea Compounds; Sorafenib; Thyroid | 2021 |
Effectiveness and safety of sorafenib for renal cell, hepatocellular and thyroid carcinoma: pooled analysis in patients with renal impairment.
Topics: Antineoplastic Agents; Carcinoma, Hepatocellular; Carcinoma, Renal Cell; Humans; Kidney; Kidney Neop | 2022 |
Quercetin improves the effects of sorafenib on growth and migration of thyroid cancer cells.
Topics: Antineoplastic Agents; Cell Line, Tumor; Cell Proliferation; Humans; Niacinamide; Phenylurea Compoun | 2020 |
Hürthle Cell Thyroid Adenoma Showing Avid Uptake on 18F-PSMA-1007 PET/CT.
Topics: Adenoma, Oxyphilic; Aged; Biological Transport; Fluorine Radioisotopes; Humans; Male; Neoplasm Stagi | 2020 |
Cost Effectiveness of Lenvatinib, Sorafenib and Placebo in Treatment of Radioiodine-Refractory Differentiated Thyroid Cancer.
Topics: Aged; Antineoplastic Agents; Cell Differentiation; Clinical Trials, Phase III as Topic; Controlled C | 2017 |
Inhibition of the AKT/mTOR Pathway Augments the Anticancer Effects of Sorafenib in Thyroid Cancer.
Topics: Antineoplastic Agents; Cell Line, Tumor; Cell Proliferation; Disease-Free Survival; Humans; Niacinam | 2017 |
Effects of sorafenib and an adenylyl cyclase activator on in vitro growth of well-differentiated thyroid cancer cells.
Topics: Adenylyl Cyclases; Cell Differentiation; Cell Proliferation; Colforsin; Cyclic AMP; Humans; MAP Kina | 2017 |
Inhibition of autophagy enhances the targeted therapeutic effect of sorafenib in thyroid cancer.
Topics: Animals; Antineoplastic Agents; Autophagy; Autophagy-Related Protein 5; Cell Line, Tumor; Chloroquin | 2018 |
Tyrosine kinase inhibitors in iodine-refractory differentiated thyroid cancer: experience in clinical practice.
Topics: Adenocarcinoma, Follicular; Adenoma, Oxyphilic; Adult; Aged; Antineoplastic Agents; Axitinib; Carcin | 2018 |
Potential role of sorafenib as neoadjuvant therapy in unresectable papillary thyroid cancer.
Topics: Antineoplastic Agents; Carcinoma, Papillary; Humans; Iodine Radioisotopes; Male; Neoadjuvant Therapy | 2018 |
Response to sorafenib in a pediatric patient with papillary thyroid carcinoma with diffuse nodular pulmonary disease requiring mechanical ventilation.
Topics: Carcinoma; Carcinoma, Papillary; Child; Humans; Hypoxia; Iodine Radioisotopes; Lung Neoplasms; Male; | 2014 |
Metabolic response demonstrated by 18F-FDG-PET/CT in metastatic medullary thyroid carcinoma under sorafenib therapy.
Topics: Antineoplastic Agents; Biomarkers, Pharmacological; Biomarkers, Tumor; Carcinoma, Neuroendocrine; Fe | 2013 |
Unilateral renal artery stenosis with renal atrophy in a patient with metastatic papillary thyroid carcinoma treated with sorafenib.
Topics: Antineoplastic Agents; Atrophy; Carcinoma; Carcinoma, Papillary; Female; Humans; Kidney; Middle Aged | 2013 |
Successful use of sorafenib after bortezomib failure in metastatic follicular thyroid cancer - a case report.
Topics: Adenocarcinoma, Follicular; Adult; Boronic Acids; Bortezomib; Female; Humans; Kidney Neoplasms; Lung | 2013 |
Pretherapeutic drug evaluation by tumor xenografting in anaplastic thyroid cancer.
Topics: Animals; Apoptosis; Benzazepines; Cell Proliferation; Drug Evaluation, Preclinical; Humans; Male; Mi | 2013 |
Sorafenib makes headway on metastatic thyroid cancer.
Topics: Humans; Neoplasm Metastasis; Niacinamide; Phenylurea Compounds; Randomized Controlled Trials as Topi | 2013 |
Critical role of sorafenib exposure over time for its antitumor activity in thyroid cancer.
Topics: Aged; Antineoplastic Agents; Female; Humans; Lung Neoplasms; Niacinamide; Phenylurea Compounds; Prot | 2014 |
Tyrosine kinase inhibitor treatments in patients with metastatic thyroid carcinomas: a retrospective study of the TUTHYREF network.
Topics: Adenocarcinoma; Adenocarcinoma, Follicular; Adenoma, Oxyphilic; Adult; Aged; Antineoplastic Agents; | 2014 |
Complete resolution of hypercortisolism with sorafenib in a patient with advanced medullary thyroid carcinoma and ectopic ACTH (adrenocorticotropic hormone) syndrome.
Topics: ACTH Syndrome, Ectopic; Carcinoma, Neuroendocrine; Humans; Male; Middle Aged; Niacinamide; Phenylure | 2014 |
Role of salvage targeted therapy in differentiated thyroid cancer patients who failed first-line sorafenib.
Topics: Adult; Aged; Antineoplastic Combined Chemotherapy Protocols; Carcinoma, Papillary, Follicular; Chemo | 2014 |
More effective agents still needed for progressive radioiodine-refractory differentiated thyroid cancer.
Topics: Antineoplastic Agents; Humans; Niacinamide; Phenylurea Compounds; Protein Kinase Inhibitors; Sorafen | 2014 |
Notable decrease of malignant pleural effusion after treatment with sorafenib in radioiodine-refractory follicular thyroid carcinoma.
Topics: Adenocarcinoma, Follicular; Humans; Male; Middle Aged; Neoplasm Recurrence, Local; Niacinamide; Phen | 2014 |
Response to sorafenib treatment in advanced metastatic thyroid cancer.
Topics: Aged; Antineoplastic Agents; Bone Neoplasms; Carcinoma, Papillary; Compassionate Use Trials; Female; | 2014 |
Efficacy and tolerability of different starting doses of sorafenib in patients with differentiated thyroid cancer.
Topics: Adenoma, Oxyphilic; Antineoplastic Agents; Carcinoma; Carcinoma, Papillary; Disease Progression; Dis | 2014 |
New era for treatment in differentiated thyroid cancer.
Topics: Antineoplastic Agents; Female; Humans; Male; Niacinamide; Phenylurea Compounds; Sorafenib; Thyroid N | 2014 |
(99m)Tc-labeled-rhTSH analogue (TR1401) for imaging poorly differentiated metastatic thyroid cancer.
Topics: Animals; Cattle; Cell Differentiation; Cell Separation; CHO Cells; Cricetinae; Cricetulus; Dogs; Flo | 2014 |
In reply.
Topics: Antineoplastic Agents; Female; Humans; Male; Niacinamide; Phenylurea Compounds; Thyroid Neoplasms | 2014 |
Sorafenib in thyroid cancer patients: learning from toxicity.
Topics: Antineoplastic Agents; Female; Humans; Male; Niacinamide; Phenylurea Compounds; Thyroid Neoplasms | 2014 |
Efficacy of sorafenib and impact on cardiac function in patients with thyroid cancer: a retrospective analysis.
Topics: Aged; Aged, 80 and over; Antineoplastic Agents; Biomarkers, Tumor; Electrocardiography; Female; Foll | 2014 |
Second-line sunitinib as a feasible approach for iodine-refractory differentiated thyroid cancer after the failure of first-line sorafenib.
Topics: Antineoplastic Agents; Disease Progression; Drug Resistance, Neoplasm; Female; Humans; Indoles; Iodi | 2015 |
To treat or not to treat: developments in the field of advanced differentiated thyroid cancer.
Topics: Adenocarcinoma, Follicular; Aged; Clinical Trials, Phase I as Topic; Drug Delivery Systems; Female; | 2014 |
Sorafenib treatment of radioiodine-refractory advanced thyroid cancer in daily clinical practice: a cohort study from a single center.
Topics: Adolescent; Adult; Aged; Antineoplastic Agents; Cohort Studies; Combined Modality Therapy; Disease-F | 2015 |
[Treatment of patients with radioiodine refractory, differentiated thyroid carcinoma. A Consensus Statement].
Topics: Antineoplastic Agents; Chemoradiotherapy; Evidence-Based Medicine; Germany; Humans; Iodine Radioisot | 2015 |
Thyroid carcinoma, version 2.2014.
Topics: Adenocarcinoma; Anilides; Carcinoma, Neuroendocrine; Guidelines as Topic; Humans; Neoplasm Metastasi | 2014 |
The proteomic 2D-DIGE approach reveals the protein voltage-dependent anion channel 2 as a potential therapeutic target in epithelial thyroid tumours.
Topics: Adolescent; Adult; Aged; Aged, 80 and over; bcl-2 Homologous Antagonist-Killer Protein; bcl-2-Associ | 2015 |
Synergistic anti-proliferative effect of metformin and sorafenib on growth of anaplastic thyroid cancer cells and their stem cells.
Topics: Antineoplastic Agents; Apoptosis; Carcinoma; Cell Cycle Checkpoints; Cell Line, Tumor; Dose-Response | 2015 |
Sorafenib for patients with differentiated thyroid cancer.
Topics: Antineoplastic Agents; Female; Humans; Male; Niacinamide; Phenylurea Compounds; Thyroid Neoplasms | 2015 |
Sorafenib for patients with differentiated thyroid cancer.
Topics: Antineoplastic Agents; Female; Humans; Male; Niacinamide; Phenylurea Compounds; Thyroid Neoplasms | 2015 |
Sorafenib for patients with differentiated thyroid cancer--authors' reply.
Topics: Antineoplastic Agents; Female; Humans; Male; Niacinamide; Phenylurea Compounds; Thyroid Neoplasms | 2015 |
Sorafenib for patients with differentiated thyroid cancer.
Topics: Antineoplastic Agents; Female; Humans; Male; Niacinamide; Phenylurea Compounds; Thyroid Neoplasms | 2015 |
Complete disappearance of liver metastases in a patient with iodine-refractory differentiated thyroid cancer subjected to sorafenib re-challenge.
Topics: Antineoplastic Agents; Female; Humans; Iodine Radioisotopes; Liver; Liver Neoplasms; Middle Aged; Ni | 2015 |
Iodide- and glucose-handling gene expression regulated by sorafenib or cabozantinib in papillary thyroid cancer.
Topics: Anilides; Antineoplastic Agents; Apoptosis; Autoantigens; Carcinoma, Papillary; Cell Cycle; Cell Lin | 2015 |
Sorafenib inhibits intracellular signaling pathways and induces cell cycle arrest and cell death in thyroid carcinoma cells irrespective of histological origin or BRAF mutational status.
Topics: Antineoplastic Agents; Cell Cycle Checkpoints; Cell Death; Cell Line, Tumor; Cell Survival; Humans; | 2015 |
Effects of Cancer Therapy Targeting Vascular Endothelial Growth Factor Receptor on Central Blood Pressure and Cardiovascular System.
Topics: Aged; Antineoplastic Agents; Arteries; Blood Pressure; Carcinoma, Renal Cell; Female; Heart; Humans; | 2016 |
Sorafenib in the treatment of thyroid cancer.
Topics: Animals; Antineoplastic Agents; Disease-Free Survival; Humans; Neoplasm Metastasis; Niacinamide; Phe | 2015 |
The Raf Kinase Inhibitor Sorafenib Inhibits JAK-STAT Signal Transduction in Human Immune Cells.
Topics: Animals; Cell Line, Tumor; Cells, Cultured; Dose-Response Relationship, Drug; Flow Cytometry; Gene E | 2015 |
[Molecular targeting treatment for thyroid cancer].
Topics: Antineoplastic Agents; Clinical Trials as Topic; Humans; Molecular Targeted Therapy; Niacinamide; Ph | 2015 |
Combinatorial anticancer effects of curcumin and sorafenib towards thyroid cancer cells via PI3K/Akt and ERK pathways.
Topics: Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Cell Line, Tumor; Cell Movement; Curcumin | 2016 |
Partial response to sorafenib treatment associated with transient grade 3 thrombocytopenia in a patient with locally advanced thyroid cancer.
Topics: Aged; Antineoplastic Agents; Female; Humans; Neoplasm Recurrence, Local; Neoplasm Staging; Niacinami | 2015 |
Case report of severe Cushing's syndrome in medullary thyroid cancer complicated by functional diabetes insipidus, aortic dissection, jejunal intussusception, and paraneoplastic dysautonomia: remission with sorafenib without reduction in cortisol concentr
Topics: Adult; Antineoplastic Agents; Aortic Aneurysm; Aortic Dissection; Carcinoma, Medullary; Cushing Synd | 2015 |
Targeted therapy for advanced or metastatic differentiated thyroid carcinoma.
Topics: Antineoplastic Agents; Drug Resistance, Neoplasm; Humans; Molecular Targeted Therapy; Neoplasm Recur | 2015 |
High Affinity Pharmacological Profiling of Dual Inhibitors Targeting RET and VEGFR2 in Inhibition of Kinase and Angiogeneis Events in Medullary Thyroid Carcinoma.
Topics: Angiogenesis Inhibitors; Anilides; Carcinoma, Neuroendocrine; Databases, Chemical; Drug Discovery; H | 2015 |
Sorafenib for the Treatment of Progressive Metastatic Medullary Thyroid Cancer: Efficacy and Safety Analysis.
Topics: Adult; Aged; Antineoplastic Agents; Carcinoma, Neuroendocrine; Disease Progression; Disease-Free Sur | 2016 |
B-Raf Inhibition in the Clinic: Present and Future.
Topics: Antineoplastic Agents; Colonic Neoplasms; Drug Resistance, Neoplasm; Humans; Imidazoles; Indoles; MA | 2016 |
(Secondary) solid tumors in thyroid cancer patients treated with the multi-kinase inhibitor sorafenib may present diagnostic challenges.
Topics: Aged; Apoptosis; Carcinogenesis; Carcinoma, Squamous Cell; Female; Humans; Male; Middle Aged; Mutati | 2016 |
pAKT Expression and Response to Sorafenib in Differentiated Thyroid Cancer.
Topics: Aged; Antineoplastic Agents; Biomarkers, Tumor; Endothelial Cells; Female; Gene Expression; Humans; | 2016 |
Sorafenib (NEXAVAR) and differentiated thyroid cancer. Toxic, and no proof of improved survival.
Topics: Antineoplastic Agents; Humans; Niacinamide; Phenylurea Compounds; Protein Kinase Inhibitors; Sorafen | 2016 |
Effects of the multikinase inhibitors Sorafenib and Regorafenib in PTEN deficient neoplasias.
Topics: Animals; Antineoplastic Agents; Carcinoma; Cell Line, Tumor; Disease Models, Animal; Endometrial Neo | 2016 |
Sorafenib and Quinacrine Target Anti-Apoptotic Protein MCL1: A Poor Prognostic Marker in Anaplastic Thyroid Cancer (ATC).
Topics: Animals; Antineoplastic Agents; Apoptosis; Apoptosis Regulatory Proteins; Biomarkers, Tumor; Cell Li | 2016 |
Efficacy of lenvatinib in treating thyroid cancer.
Topics: Biomarkers; Calcitonin; Carcinoma, Neuroendocrine; Clinical Trials as Topic; Half-Life; Humans; Niac | 2016 |
68Ga DOTATATE PET/CT in Differentiated Thyroid Carcinoma With Fibular Metastasis and Mixed Response to Sorafenib.
Topics: Female; Humans; Middle Aged; Neoplasm Metastasis; Niacinamide; Organometallic Compounds; Phenylurea | 2016 |
[Lenvatinib in radioiodine refractory thyroid carcinomas].
Topics: Adenocarcinoma, Follicular; Antineoplastic Agents; Clinical Trials as Topic; Compassionate Use Trial | 2016 |
Timing of multikinase inhibitor initiation in differentiated thyroid cancer.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Carcinoma; Drug Administration Schedule; Fema | 2017 |
Targeted therapeutic approach for an anaplastic thyroid cancer in vitro and in vivo.
Topics: Antineoplastic Agents; Benzenesulfonates; Boronic Acids; Bortezomib; Carcinoma; Cell Line, Tumor; Hu | 2008 |
Sorafenib potently inhibits papillary thyroid carcinomas harboring RET/PTC1 rearrangement.
Topics: Animals; Antineoplastic Agents; Benzenesulfonates; Carcinoma, Papillary; Cell Line, Tumor; Cell Prol | 2008 |
Sorafenib-induced liver failure.
Topics: Adenocarcinoma, Follicular; Aged; Antineoplastic Agents; Benzenesulfonates; Female; Humans; Liver Fa | 2008 |
Motesanib diphosphate in progressive differentiated thyroid cancer.
Topics: Adenocarcinoma, Follicular; Biomarkers, Tumor; Disease Progression; Humans; Indoles; Mitogen-Activat | 2008 |
The successful use of sorafenib to treat pediatric papillary thyroid carcinoma.
Topics: Adolescent; Benzenesulfonates; Carcinoma, Papillary; Child; Female; Humans; Iodine Radioisotopes; Lu | 2009 |
Sorafenib induces partial response in metastatic medullary thyroid carcinoma.
Topics: Adult; Antineoplastic Agents; Benzenesulfonates; Bone Neoplasms; Carcinoma, Neuroendocrine; Humans; | 2010 |
Proliferation and survival molecules implicated in the inhibition of BRAF pathway in thyroid cancer cells harbouring different genetic mutations.
Topics: Apoptosis; Apoptosis Regulatory Proteins; Benzenesulfonates; Cell Line, Tumor; Cell Proliferation; C | 2009 |
Inhibition of tumor angiogenesis by the matrix metalloproteinase-activated anthrax lethal toxin in an orthotopic model of anaplastic thyroid carcinoma.
Topics: Animals; Antigens, Bacterial; Bacterial Toxins; Benzenesulfonates; Carcinoma; Cell Line, Tumor; Cell | 2010 |
Sorafenib-induced psoriasiform eruption in a patient with metastatic thyroid carcinoma.
Topics: Antineoplastic Agents; Benzenesulfonates; Drug Eruptions; Humans; Male; Middle Aged; Neoplasm Metast | 2010 |
Treatment with tyrosine kinase inhibitors for patients with differentiated thyroid cancer: the M. D. Anderson experience.
Topics: Adult; Aged; Aged, 80 and over; Antineoplastic Agents; Benzenesulfonates; Disease Progression; Disea | 2010 |
Harvesting the low-hanging fruit: kinase inhibitors for therapy of advanced medullary and nonmedullary thyroid cancer.
Topics: Adenocarcinoma, Follicular; Antineoplastic Agents; Benzenesulfonates; Biomarkers, Tumor; Carcinoma, | 2010 |
Parenchymal versus nonparenchymal target lesion response in clinical trials for metastatic medullary thyroid cancer.
Topics: Administration, Oral; Benzenesulfonates; Biomarkers, Tumor; Calcitonin; Carcinoembryonic Antigen; Ca | 2010 |
Rapid response to sorafenib in metastatic medullary thyroid carcinoma.
Topics: Antineoplastic Agents; Benzenesulfonates; Calcitonin; Carcinoembryonic Antigen; Carcinoma, Neuroendo | 2011 |
Population pharmacokinetic/pharmacodynamic modeling for the time course of tumor shrinkage by motesanib in thyroid cancer patients.
Topics: Adult; Aged; Antineoplastic Agents; Area Under Curve; Carcinoma, Medullary; Drug Administration Sche | 2010 |
Development of a modeling framework to simulate efficacy endpoints for motesanib in patients with thyroid cancer.
Topics: Adult; Aged; Antineoplastic Agents; Area Under Curve; Disease-Free Survival; Dose-Response Relations | 2010 |
Mitochondrial localization and regulation of BRAFV600E in thyroid cancer: a clinically used RAF inhibitor is unable to block the mitochondrial activities of BRAFV600E.
Topics: Animals; Apoptosis; Benzenesulfonates; Blotting, Western; Cell Line, Tumor; Cell Proliferation; Cell | 2011 |
Fatal heart failure after a 26-month combination of tyrosine kinase inhibitors in a papillary thyroid cancer.
Topics: Acute Coronary Syndrome; Benzamides; Benzenesulfonates; Carcinoma; Carcinoma, Papillary; Fatal Outco | 2011 |
Anti-tumor activity of motesanib in a medullary thyroid cancer model.
Topics: Animals; Antineoplastic Agents; Carcinoma, Neuroendocrine; Cell Line, Tumor; Cells, Cultured; Female | 2012 |
A painful cranial bulge.
Topics: Adenocarcinoma, Follicular; Antineoplastic Agents; Benzenesulfonates; Brain Neoplasms; Drug Administ | 2011 |
Laryngeal metastasis as first presentation of hepatocellular carcinoma.
Topics: Adenoma, Oxyphilic; Antineoplastic Agents; Biopsy, Fine-Needle; Carcinoma, Hepatocellular; Combined | 2011 |
[New therapeutic options for advanced thyroid cancer].
Topics: Antineoplastic Agents; Benzenesulfonates; Humans; Indoles; Niacinamide; Phenylurea Compounds; Piperi | 2011 |
Transient partial response to sorafenib treatment in an adolescent patient with MEN2B syndrome and end-stage medullary thyroid carcinoma.
Topics: Adolescent; Antineoplastic Agents; Benzenesulfonates; Carcinoma, Medullary; Female; Humans; Multiple | 2012 |
The urokinase plasminogen activator system in metastatic papillary thyroid carcinoma: a potential therapeutic target.
Topics: Antineoplastic Agents; Benzenesulfonates; Carcinoma, Papillary; Humans; Iodine Radioisotopes; Neopla | 2011 |
[Long-standing differentiated thyroid carcinoma].
Topics: Antineoplastic Agents; Benzenesulfonates; Biopsy, Needle; Carcinoma, Large Cell; Carcinoma, Papillar | 2012 |
Sorafenib and Mek inhibition is synergistic in medullary thyroid carcinoma in vitro.
Topics: Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Benzenesulfonates; Benzimidaz | 2012 |
Sorafenib in metastatic thyroid cancer.
Topics: Adult; Antineoplastic Agents; Benzenesulfonates; Calcitonin; Carcinoembryonic Antigen; Disease-Free | 2012 |
[Endocrinology].
Topics: ACTH-Secreting Pituitary Adenoma; Adenoma; Benzenesulfonates; Carcinoma; Carcinoma, Medullary; Clini | 2012 |
Pancreatic metastasis arising from a BRAF(V600E)-positive papillary thyroid cancer: the role of endoscopic ultrasound-guided biopsy and response to sorafenib therapy.
Topics: Benzenesulfonates; Biopsy; Carcinoma; Carcinoma, Papillary; Disease Progression; Endoscopy; Fatal Ou | 2012 |
Therapeutic management of metastatic medullary thyroid carcinoma: role of new tyrosine kinase inhibitors.
Topics: Carcinoma, Neuroendocrine; Humans; Lymphatic Metastasis; Male; Middle Aged; Niacinamide; Phenylurea | 2013 |
Unusual short-term complete response to two regimens of cytotoxic chemotherapy in a patient with poorly differentiated thyroid carcinoma.
Topics: Antibiotics, Antineoplastic; Antineoplastic Agents, Phytogenic; Antineoplastic Combined Chemotherapy | 2012 |
Functional characterization of the novel BRAF complex mutation, BRAF(V600delinsYM) , identified in papillary thyroid carcinoma.
Topics: 3T3 Cells; Amino Acid Substitution; Animals; Benzenesulfonates; Carcinoma; Carcinoma, Papillary; Cel | 2013 |
Brain metastasis from follicular thyroid carcinoma: treatment with sorafenib.
Topics: Adenocarcinoma, Follicular; Antineoplastic Agents; Benzenesulfonates; Brain Neoplasms; Female; Human | 2012 |
Sorafenib in advanced iodine-refractory differentiated thyroid cancer: efficacy, safety and exploratory analysis of role of serum thyroglobulin and FDG-PET.
Topics: Antineoplastic Agents; Female; Fluorodeoxyglucose F18; Humans; Male; Middle Aged; Niacinamide; Pheny | 2013 |
Sorafenib therapy decreases the clearance of thyrotropin.
Topics: Aged; Aged, 80 and over; Carcinoma; Dose-Response Relationship, Drug; Female; Humans; Male; Middle A | 2013 |
Autophagic activation potentiates the antiproliferative effects of tyrosine kinase inhibitors in medullary thyroid cancer.
Topics: Antineoplastic Agents; Autophagy; Benzenesulfonates; Benzimidazoles; Carcinoma, Neuroendocrine; Cell | 2012 |
A novel combination of withaferin A and sorafenib shows synergistic efficacy against both papillary and anaplastic thyroid cancers.
Topics: Antineoplastic Agents; Apoptosis; Benzenesulfonates; Blotting, Western; Carcinoma; Carcinoma, Papill | 2012 |
[Effects of sorafenib and liposome doxorubicin on human poorly differentiated thyroid carcinoma xenografts in nude mice].
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Doxorubicin; Humans; Liposomes; Mice; Mice, | 2012 |
Nicotinamide increases thyroid radiosensitivity by stimulating nitric oxide synthase expression and the generation of organic peroxides.
Topics: Animals; Gene Expression Regulation, Enzymologic; Hyperthyroidism; Iodine Radioisotopes; Male; Niaci | 2006 |
BAY 43-9006 inhibition of oncogenic RET mutants.
Topics: Administration, Oral; Animals; Antineoplastic Agents; Benzenesulfonates; Cell Cycle; Drug Administra | 2006 |
BRAF is a therapeutic target in aggressive thyroid carcinoma.
Topics: Animals; Benzenesulfonates; Carcinoma; Carcinoma, Papillary; Cell Proliferation; Humans; Male; Mice; | 2006 |
Sorafenib inhibits the angiogenesis and growth of orthotopic anaplastic thyroid carcinoma xenografts in nude mice.
Topics: Angiogenesis Inhibitors; Animals; Apoptosis; Benzenesulfonates; Cell Division; Humans; Immunohistoch | 2007 |
Optimization of boron neutron capture therapy for the treatment of undifferentiated thyroid cancer.
Topics: Animals; Apoptosis; Boron Compounds; Boron Neutron Capture Therapy; Cell Line, Tumor; Deuteroporphyr | 2007 |
Medullary thyroid cancer: targeting the RET kinase pathway with sorafenib/tipifarnib.
Topics: Adult; Amino Acid Sequence; Antineoplastic Agents; Benzenesulfonates; Carcinoma, Medullary; Cell Lin | 2008 |
Notes on streptozotocin in metastatic insulinoma.
Topics: Adenoma, Islet Cell; Adult; Antibiotics, Antineoplastic; Autopsy; Blood Glucose; Bone Marrow; Brain; | 1971 |