entinostat has been researched along with Lung Neoplasms in 25 studies
Lung Neoplasms: Tumors or cancer of the LUNG.
Excerpt | Relevance | Reference |
---|---|---|
"Addition of entinostat to atezolizumab, carboplatin, and etoposide is unsafe and resulted in early onset and severe neutropenia, thrombocytopenia." | 5.69 | Phase I Study of Entinostat, Atezolizumab, Carboplatin, and Etoposide in Previously Untreated Extensive-Stage Small Cell Lung Cancer, ETCTN 10399. ( Bullock, TN; Carducci, MA; Gentzler, RD; Hanley, M; Horton, B; Kim, K; Mock, J; Park, KS; Phelps, MA; Piekarz, R; Rhee, JC; Rudek, MA; Rudin, CM; Villaruz, LC, 2023) |
"Entinostat is a selective HDAC inhibitor that has shown anti-neoplastic activity and tolerability in hematologic and solid tumors, including lung cancer." | 2.52 | Entinostat (SNDX-275) for the treatment of non-small cell lung cancer. ( Raez, LE; Rolfo, C; Ruiz, R, 2015) |
" The subcutaneous dosing route for consecutive days and reduced bioavailability of 5-azacytidine because of inactivation by cytidine deaminase may limit the expansion of epigenetic therapy into Phase III trials." | 1.39 | Aerosolised 5-azacytidine suppresses tumour growth and reprogrammes the epigenome in an orthotopic lung cancer model. ( Belinsky, SA; Cheng, YS; Grimes, MJ; Kuehl, PJ; March, TH; Picchi, MA; Reed, MD; Tellez, CS; Tessema, M, 2013) |
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 0 (0.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 3 (12.00) | 29.6817 |
2010's | 19 (76.00) | 24.3611 |
2020's | 3 (12.00) | 2.80 |
Authors | Studies |
---|---|
Gentzler, RD | 1 |
Villaruz, LC | 1 |
Rhee, JC | 1 |
Horton, B | 1 |
Mock, J | 1 |
Hanley, M | 1 |
Kim, K | 1 |
Rudek, MA | 2 |
Phelps, MA | 1 |
Carducci, MA | 1 |
Piekarz, R | 1 |
Park, KS | 1 |
Bullock, TN | 1 |
Rudin, CM | 3 |
Solta, A | 1 |
Boettiger, K | 1 |
Kovács, I | 1 |
Lang, C | 1 |
Megyesfalvi, Z | 1 |
Ferk, F | 1 |
Mišík, M | 1 |
Hoetzenecker, K | 1 |
Aigner, C | 1 |
Kowol, CR | 1 |
Knasmueller, S | 1 |
Grusch, M | 1 |
Szeitz, B | 1 |
Rezeli, M | 1 |
Dome, B | 1 |
Schelch, K | 1 |
Hellmann, MD | 1 |
Jänne, PA | 1 |
Opyrchal, M | 1 |
Hafez, N | 1 |
Raez, LE | 2 |
Gabrilovich, DI | 1 |
Wang, F | 2 |
Trepel, JB | 1 |
Lee, MJ | 1 |
Yuno, A | 1 |
Lee, S | 1 |
Brouwer, S | 1 |
Sankoh, S | 1 |
Wang, L | 1 |
Tamang, D | 1 |
Schmidt, EV | 1 |
Meyers, ML | 1 |
Ramalingam, SS | 1 |
Shum, E | 1 |
Ordentlich, P | 1 |
Gurunathan, S | 1 |
Kang, MH | 1 |
Kim, JH | 1 |
Luo, BL | 1 |
Zhou, Y | 1 |
Lv, H | 1 |
Sun, SH | 1 |
Tang, WX | 1 |
Rao-Bindal, K | 2 |
Koshkina, NV | 2 |
Stewart, J | 1 |
Kleinerman, ES | 3 |
Murray-Stewart, T | 1 |
Hanigan, CL | 1 |
Woster, PM | 1 |
Marton, LJ | 1 |
Casero, RA | 2 |
Reed, MD | 3 |
Tellez, CS | 3 |
Grimes, MJ | 3 |
Picchi, MA | 3 |
Tessema, M | 1 |
Cheng, YS | 1 |
March, TH | 3 |
Kuehl, PJ | 1 |
Belinsky, SA | 4 |
Yokobori, T | 1 |
Yokoyama, Y | 1 |
Mogi, A | 1 |
Endoh, H | 1 |
Altan, B | 1 |
Kosaka, T | 1 |
Yamaki, E | 1 |
Yajima, T | 1 |
Tomizawa, K | 1 |
Azuma, Y | 1 |
Onozato, R | 1 |
Miyazaki, T | 1 |
Tanaka, S | 1 |
Kuwano, H | 1 |
Liu, Y | 2 |
Oganesian, A | 1 |
Taverna, P | 1 |
Huang, G | 1 |
Nishimoto, K | 1 |
Yang, Y | 1 |
Vendetti, FP | 2 |
Topper, M | 1 |
Huang, P | 1 |
Dobromilskaya, I | 1 |
Easwaran, H | 1 |
Wrangle, J | 2 |
Baylin, SB | 3 |
Poirier, JT | 1 |
Ruiz, R | 1 |
Rolfo, C | 1 |
Weintraub, K | 1 |
Carter, CA | 1 |
Zeman, K | 1 |
Day, RM | 1 |
Richard, P | 1 |
Oronsky, A | 1 |
Oronsky, N | 1 |
Lybeck, M | 1 |
Scicinski, J | 1 |
Oronsky, B | 1 |
Wang, S | 1 |
Zhu, L | 1 |
Zuo, W | 1 |
Zeng, Z | 1 |
Huang, L | 1 |
Lin, F | 1 |
Lin, R | 1 |
Wang, J | 1 |
Lu, J | 1 |
Wang, Q | 1 |
Lin, L | 1 |
Dong, H | 1 |
Wu, W | 1 |
Zheng, K | 1 |
Cai, J | 1 |
Yang, S | 1 |
Ma, Y | 1 |
Ye, S | 1 |
Liu, W | 1 |
Yu, Y | 1 |
Tan, J | 1 |
Liu, B | 1 |
Yong, KJ | 1 |
Li, A | 1 |
Ou, WB | 1 |
Hong, CK | 1 |
Zhao, W | 1 |
Tatetsu, H | 1 |
Yan, B | 1 |
Qi, L | 1 |
Fletcher, JA | 1 |
Yang, H | 1 |
Soo, R | 1 |
Tenen, DG | 1 |
Chai, L | 1 |
Niesen, MI | 1 |
Blanck, G | 1 |
Kakihana, M | 1 |
Ohira, T | 1 |
Chan, D | 2 |
Webster, RB | 1 |
Kato, H | 1 |
Drabkin, HA | 1 |
Gemmill, RM | 1 |
Mitchell, HD | 1 |
Stidley, CA | 1 |
Tesfaigzi, Y | 1 |
Channell, MM | 1 |
Witta, SE | 1 |
Jotte, RM | 1 |
Konduri, K | 1 |
Neubauer, MA | 1 |
Spira, AI | 1 |
Ruxer, RL | 1 |
Varella-Garcia, M | 1 |
Bunn, PA | 1 |
Hirsch, FR | 1 |
Juergens, RA | 1 |
Murphy, SC | 1 |
Zhao, M | 1 |
Coleman, B | 1 |
Sebree, R | 1 |
Rodgers, K | 1 |
Hooker, CM | 1 |
Franco, N | 1 |
Lee, B | 1 |
Tsai, S | 1 |
Delgado, IE | 1 |
Herman, JG | 1 |
Brock, MV | 1 |
Nagathihalli, NS | 1 |
Massion, PP | 1 |
Gonzalez, AL | 1 |
Lu, P | 1 |
Datta, PK | 1 |
Moody, TW | 1 |
Nakagawa, T | 1 |
Kang, Y | 1 |
Jakowlew, S | 1 |
Jensen, RT | 1 |
Trial | Phase | Enrollment | Study Type | Start Date | Status | ||
---|---|---|---|---|---|---|---|
A Phase 1b/2, Open-label, Dose Escalation Study of Entinostat in Combination With Pembrolizumab in Patients With Non-small Cell Lung Cancer, With Expansion Cohorts in Patients With Non-small Cell Lung Cancer, Melanoma, and Mismatch Repair-Proficient Color[NCT02437136] | Phase 1/Phase 2 | 196 participants (Actual) | Interventional | 2015-07-31 | Completed | ||
A Phase I Study to Assess the Food Effect on the Pharmacokinetics of Entinostat in Postmenopausal Women With Locally Recurrent or Metastatic ER+ Breast Cancer and Men and Women With Progressive Non-Small Cell Lung Cancer[NCT01594398] | Phase 1 | 14 participants (Actual) | Interventional | 2012-05-31 | Completed | ||
A Phase I Study of Entinostat in Combination With Enzalutamide for Treatment of Patients With Castration-Resistant Prostate Cancer[NCT03829930] | Phase 1 | 6 participants (Actual) | Interventional | 2019-05-01 | Terminated (stopped due to Sponsor discontinued the drug) | ||
A Phase I/II Study of Entinostat in Combination With 5-Azacytidine in Patients With Recurrent Advanced Non-Small Cell Lung Cancer[NCT00387465] | Phase 1/Phase 2 | 94 participants (Actual) | Interventional | 2006-08-31 | Completed | ||
Phase 1b/2a Safety and Immunogenicity of the DNMT Inhibitor Azacitidine During Anti-Tuberculosis Therapy[NCT03941496] | Phase 1/Phase 2 | 0 participants (Actual) | Interventional | 2022-10-31 | Withdrawn (stopped due to The study was halted prematurely due to Bristol-Myers Squibb's (BMS) decision to withdraw support for this study.) | ||
[information is prepared from clinicaltrials.gov, extracted Sep-2024] |
DLT is defined by the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI CTCAE) v3.0 (NCT00387465)
Timeframe: Up to 28 days
Intervention | Participants (Count of Participants) |
---|---|
Phase I - 30mg/m2 Azacitidine | 0 |
Phase I - 40mg/m2 Azacitidine | 0 |
"Number of participants with decrease in DNA methylation (methylation-signature positive) on Day 10 or Day 29, and either stable disease or objective response (OR) as defined by RECIST 1.0. Per RECIST 1.0, progression is defined as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions; PR is defined as >=30% decrease in the sum of the longest diameter of target lesions, complete response is defined as disappearance of all target lesions; OR=CR+PR." (NCT00387465)
Timeframe: Baseline and days 10 and 29
Intervention | Participants (Count of Participants) |
---|---|
Azacitidine 40mg/m2 With Entinostat | 8 |
Determined by the method determined by Kaplan and Meier. 95% confidence intervals will be estimated. (NCT00387465)
Timeframe: Up to 1 year
Intervention | months (Median) |
---|---|
Azacitidine 40mg/m2 With Entinostat | 6.4 |
(NCT00387465)
Timeframe: Day 1
Intervention | ng*hr/mL (Mean) |
---|---|
Azacitidine 40mg/m2 With Entinostat | 675 |
Maximal concentration (ng/mL) of azacitidine (NCT00387465)
Timeframe: Day 1
Intervention | ng/mL (Mean) |
---|---|
Azacitidine 40mg/m2 With Entinostat | 468 |
(NCT00387465)
Timeframe: Day 1
Intervention | hours (Mean) |
---|---|
Azacitidine 40mg/m2 With Entinostat | 1.12 |
Time to maximal concentration of azacitidine in the blood. (NCT00387465)
Timeframe: Day 1
Intervention | hours (Median) |
---|---|
Azacitidine 40mg/m2 With Entinostat | 0.5 |
Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions. Determined by the method determined by Kaplan and Meier. 95% confidence intervals will be estimated. (NCT00387465)
Timeframe: Up to 1 year
Intervention | weeks (Median) |
---|---|
Azacitidine 40mg/m2 With Entinostat | 7.4 |
(NCT00387465)
Timeframe: Day 10 and 17
Intervention | ng/mL (Mean) | |
---|---|---|
Day 10 | Day 17 | |
Azacitidine 40mg/m2 With Entinostat | 0.84 | 1.10 |
3 reviews available for entinostat and Lung Neoplasms
Article | Year |
---|---|
Participation of the Fas/FasL signaling pathway and the lung microenvironment in the development of osteosarcoma lung metastases.
Topics: Animals; Antineoplastic Agents; Benzamides; Bone Neoplasms; Deoxycytidine; Epigenesis, Genetic; Fas | 2014 |
Entinostat (SNDX-275) for the treatment of non-small cell lung cancer.
Topics: Animals; Antineoplastic Agents; Benzamides; Carcinoma, Non-Small-Cell Lung; Epigenesis, Genetic; His | 2015 |
Addressing the elephant in the room, therapeutic resistance in non-small cell lung cancer, with epigenetic therapies.
Topics: Antibodies, Monoclonal; Azacitidine; Azetidines; Benzamides; Biomarkers, Tumor; Carcinoma, Non-Small | 2016 |
4 trials available for entinostat and Lung Neoplasms
Article | Year |
---|---|
Phase I Study of Entinostat, Atezolizumab, Carboplatin, and Etoposide in Previously Untreated Extensive-Stage Small Cell Lung Cancer, ETCTN 10399.
Topics: Anemia; Antineoplastic Combined Chemotherapy Protocols; Bayes Theorem; Carboplatin; Etoposide; Femal | 2023 |
Entinostat plus Pembrolizumab in Patients with Metastatic NSCLC Previously Treated with Anti-PD-(L)1 Therapy.
Topics: Aged; Aged, 80 and over; Antibodies, Monoclonal, Humanized; Antineoplastic Combined Chemotherapy Pro | 2021 |
Randomized phase II trial of erlotinib with and without entinostat in patients with advanced non-small-cell lung cancer who progressed on prior chemotherapy.
Topics: Aged; Antineoplastic Combined Chemotherapy Protocols; Benzamides; Biomarkers, Tumor; Cadherins; Carc | 2012 |
Randomized phase II trial of erlotinib with and without entinostat in patients with advanced non-small-cell lung cancer who progressed on prior chemotherapy.
Topics: Aged; Antineoplastic Combined Chemotherapy Protocols; Benzamides; Biomarkers, Tumor; Cadherins; Carc | 2012 |
Randomized phase II trial of erlotinib with and without entinostat in patients with advanced non-small-cell lung cancer who progressed on prior chemotherapy.
Topics: Aged; Antineoplastic Combined Chemotherapy Protocols; Benzamides; Biomarkers, Tumor; Cadherins; Carc | 2012 |
Randomized phase II trial of erlotinib with and without entinostat in patients with advanced non-small-cell lung cancer who progressed on prior chemotherapy.
Topics: Aged; Antineoplastic Combined Chemotherapy Protocols; Benzamides; Biomarkers, Tumor; Cadherins; Carc | 2012 |
Combination epigenetic therapy has efficacy in patients with refractory advanced non-small cell lung cancer.
Topics: Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Azacitidine; Benzamides; Bi | 2011 |
Combination epigenetic therapy has efficacy in patients with refractory advanced non-small cell lung cancer.
Topics: Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Azacitidine; Benzamides; Bi | 2011 |
Combination epigenetic therapy has efficacy in patients with refractory advanced non-small cell lung cancer.
Topics: Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Azacitidine; Benzamides; Bi | 2011 |
Combination epigenetic therapy has efficacy in patients with refractory advanced non-small cell lung cancer.
Topics: Aged; Aged, 80 and over; Antineoplastic Combined Chemotherapy Protocols; Azacitidine; Benzamides; Bi | 2011 |
18 other studies available for entinostat and Lung Neoplasms
Article | Year |
---|---|
Entinostat Enhances the Efficacy of Chemotherapy in Small Cell Lung Cancer Through S-phase Arrest and Decreased Base Excision Repair.
Topics: Apoptosis; Cell Line, Tumor; Cisplatin; DNA Repair; Histone Deacetylase Inhibitors; Humans; Lung Neo | 2023 |
Combination Effect of Silver Nanoparticles and Histone Deacetylases Inhibitor in Human Alveolar Basal Epithelial Cells.
Topics: A549 Cells; Antineoplastic Agents; Apoptosis; Benzamides; Caspase 3; Cell Survival; DNA Fragmentatio | 2018 |
MS-275 potentiates the effect of YM-155 in lung adenocarcinoma via survivin downregulation induced by miR-138 and miR-195.
Topics: A549 Cells; Adenocarcinoma of Lung; Animals; Benzamides; Cell Line, Tumor; Cell Proliferation; Cell | 2019 |
The histone deacetylase inhibitor, MS-275 (entinostat), downregulates c-FLIP, sensitizes osteosarcoma cells to FasL, and induces the regression of osteosarcoma lung metastases.
Topics: Animals; Antineoplastic Agents; Apoptosis; Benzamides; Blotting, Western; Bone Neoplasms; CASP8 and | 2013 |
Histone deacetylase inhibition overcomes drug resistance through a miRNA-dependent mechanism.
Topics: Acetyltransferases; Benzamides; Cell Line, Tumor; Drug Resistance, Neoplasm; Drug Synergism; Humans; | 2013 |
Aerosolised 5-azacytidine suppresses tumour growth and reprogrammes the epigenome in an orthotopic lung cancer model.
Topics: Administration, Inhalation; Aerosols; Animals; Antimetabolites, Antineoplastic; Azacitidine; Benzami | 2013 |
FBXW7 mediates chemotherapeutic sensitivity and prognosis in NSCLCs.
Topics: Adult; Aged; Aged, 80 and over; Antigens, Neoplasm; Antineoplastic Agents; Benzamides; Carcinoma, No | 2014 |
SGI-110 and entinostat therapy reduces lung tumor burden and reprograms the epigenome.
Topics: Animals; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Azacitidine; Benzami | 2014 |
Evaluation of azacitidine and entinostat as sensitization agents to cytotoxic chemotherapy in preclinical models of non-small cell lung cancer.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Azacitidine; Benzamides; Camptothecin; Carc | 2015 |
Take two: Combining immunotherapy with epigenetic drugs to tackle cancer.
Topics: Antibodies, Monoclonal; Antineoplastic Combined Chemotherapy Protocols; Azacitidine; Benzamides; Car | 2016 |
MicroRNA-mediated epigenetic targeting of Survivin significantly enhances the antitumor activity of paclitaxel against non-small cell lung cancer.
Topics: Antineoplastic Agents; Apoptosis; Benzamides; Carcinoma, Non-Small-Cell Lung; Cell Proliferation; DN | 2016 |
Targeting SALL4 by entinostat in lung cancer.
Topics: Animals; Antineoplastic Agents; Benzamides; Cell Line, Tumor; Cell Survival; Disease Models, Animal; | 2016 |
Rescue of major histocompatibility-DR surface expression in retinoblastoma-defective, non-small cell lung carcinoma cells by the MS-275 histone deacetylase inhibitor.
Topics: Antineoplastic Agents; Benzamides; Carcinoma, Non-Small-Cell Lung; Cell Line, Tumor; Histone Deacety | 2009 |
Induction of E-cadherin in lung cancer and interaction with growth suppression by histone deacetylase inhibition.
Topics: Animals; Antineoplastic Agents; Apoptosis; Benzamides; Benzoquinones; Blotting, Western; Cadherins; | 2009 |
Combination therapy with vidaza and entinostat suppresses tumor growth and reprograms the epigenome in an orthotopic lung cancer model.
Topics: Animals; Antineoplastic Combined Chemotherapy Protocols; Apoptosis; Azacitidine; Benzamides; Cell Li | 2011 |
Effect of the histone deacetylase inhibitor SNDX-275 on Fas signaling in osteosarcoma cells and the feasibility of its topical application for the treatment of osteosarcoma lung metastases.
Topics: Administration, Inhalation; Animals; Base Sequence; Benzamides; Blotting, Western; Cell Line, Tumor; | 2011 |
Smoking induces epithelial-to-mesenchymal transition in non-small cell lung cancer through HDAC-mediated downregulation of E-cadherin.
Topics: Acetylation; Antigens, CD; Benzamides; Cadherins; Carcinoma, Non-Small-Cell Lung; Cell Movement; Dow | 2012 |
Bombesin/gastrin-releasing peptide receptor antagonists increase the ability of histone deacetylase inhibitors to reduce lung cancer proliferation.
Topics: Animals; Benzamides; Cell Line, Tumor; Cell Proliferation; Formazans; Genes, Tumor Suppressor; Histo | 2006 |