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Continuous Versus 1-Year Fixed-Duration Nivolumab in Previously Treated Advanced Non–Small-Cell Lung Cancer: CheckMate 153
Limited data exist on the optimal duration of immunotherapy, including for non–small-cell lung cancer (NSCLC). We present an exploratory analysis of CheckMate 153, a largely community-based phase IIIb/IV study, to evaluate the impact of 1-year fixed-duration versus continuous therapy on the efficacy...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society of Clinical Oncology
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7676888/ https://www.ncbi.nlm.nih.gov/pubmed/32910710 http://dx.doi.org/10.1200/JCO.20.00131 |
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author | Waterhouse, David M. Garon, Edward B. Chandler, Jason McCleod, Michael Hussein, Maen Jotte, Robert Horn, Leora Daniel, Davey B. Keogh, George Creelan, Ben Einhorn, Lawrence H. Baker, Justin Kasbari, Samer Nikolinakos, Petros Babu, Sunil Couture, Felix Leighl, Natasha B. Reynolds, Craig Blumenschein, George Gunuganti, Vijay Li, Ang Aanur, Nivedita Spigel, David R. |
author_facet | Waterhouse, David M. Garon, Edward B. Chandler, Jason McCleod, Michael Hussein, Maen Jotte, Robert Horn, Leora Daniel, Davey B. Keogh, George Creelan, Ben Einhorn, Lawrence H. Baker, Justin Kasbari, Samer Nikolinakos, Petros Babu, Sunil Couture, Felix Leighl, Natasha B. Reynolds, Craig Blumenschein, George Gunuganti, Vijay Li, Ang Aanur, Nivedita Spigel, David R. |
author_sort | Waterhouse, David M. |
collection | PubMed |
description | Limited data exist on the optimal duration of immunotherapy, including for non–small-cell lung cancer (NSCLC). We present an exploratory analysis of CheckMate 153, a largely community-based phase IIIb/IV study, to evaluate the impact of 1-year fixed-duration versus continuous therapy on the efficacy and safety of nivolumab. METHODS: Patients with previously treated advanced NSCLC received nivolumab monotherapy (3 mg/kg every 2 weeks). Those still receiving treatment at 1 year, including patients perceived to be deriving benefit despite radiographic progression, were randomly assigned to continue nivolumab until disease progression or unacceptable toxicity or to stop nivolumab with the option of on-study retreatment after disease progression (1-year fixed duration). RESULTS: Of 1,428 patients treated, 252 were randomly assigned to continuous (n = 127) or 1-year fixed-duration (n = 125) treatment (intent-to-treat [ITT] population). Of these, 89 and 85 patients in the continuous and 1-year fixed-duration arms, respectively, had not progressed (progression-free survival [PFS] population). With minimum post–random assignment follow-up of 13.5 months, median PFS was longer with continuous versus 1-year fixed-duration treatment (PFS population: 24.7 months v 9.4 months; hazard ratio [HR], 0.56 [95% CI, 0.37 to 0.84]). Median overall survival from random assignment was longer with continuous versus 1-year fixed-duration treatment in the PFS (not reached v 32.5 months; HR, 0.61 [95% CI, 0.37 to 0.99]) and ITT (not reached v 28.8 months; HR, 0.62 [95% CI, 0.42 to 0.92]) populations. Few new-onset treatment-related adverse events occurred. No new safety signals were identified. CONCLUSION: To our knowledge, these findings from an exploratory analysis represent the first randomized data on continuous versus fixed-duration immunotherapy in previously treated advanced NSCLC and suggest that continuing nivolumab beyond 1 year improves outcomes. |
format | Online Article Text |
id | pubmed-7676888 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Society of Clinical Oncology |
record_format | MEDLINE/PubMed |
spelling | pubmed-76768882021-11-20 Continuous Versus 1-Year Fixed-Duration Nivolumab in Previously Treated Advanced Non–Small-Cell Lung Cancer: CheckMate 153 Waterhouse, David M. Garon, Edward B. Chandler, Jason McCleod, Michael Hussein, Maen Jotte, Robert Horn, Leora Daniel, Davey B. Keogh, George Creelan, Ben Einhorn, Lawrence H. Baker, Justin Kasbari, Samer Nikolinakos, Petros Babu, Sunil Couture, Felix Leighl, Natasha B. Reynolds, Craig Blumenschein, George Gunuganti, Vijay Li, Ang Aanur, Nivedita Spigel, David R. J Clin Oncol ORIGINAL REPORTS Limited data exist on the optimal duration of immunotherapy, including for non–small-cell lung cancer (NSCLC). We present an exploratory analysis of CheckMate 153, a largely community-based phase IIIb/IV study, to evaluate the impact of 1-year fixed-duration versus continuous therapy on the efficacy and safety of nivolumab. METHODS: Patients with previously treated advanced NSCLC received nivolumab monotherapy (3 mg/kg every 2 weeks). Those still receiving treatment at 1 year, including patients perceived to be deriving benefit despite radiographic progression, were randomly assigned to continue nivolumab until disease progression or unacceptable toxicity or to stop nivolumab with the option of on-study retreatment after disease progression (1-year fixed duration). RESULTS: Of 1,428 patients treated, 252 were randomly assigned to continuous (n = 127) or 1-year fixed-duration (n = 125) treatment (intent-to-treat [ITT] population). Of these, 89 and 85 patients in the continuous and 1-year fixed-duration arms, respectively, had not progressed (progression-free survival [PFS] population). With minimum post–random assignment follow-up of 13.5 months, median PFS was longer with continuous versus 1-year fixed-duration treatment (PFS population: 24.7 months v 9.4 months; hazard ratio [HR], 0.56 [95% CI, 0.37 to 0.84]). Median overall survival from random assignment was longer with continuous versus 1-year fixed-duration treatment in the PFS (not reached v 32.5 months; HR, 0.61 [95% CI, 0.37 to 0.99]) and ITT (not reached v 28.8 months; HR, 0.62 [95% CI, 0.42 to 0.92]) populations. Few new-onset treatment-related adverse events occurred. No new safety signals were identified. CONCLUSION: To our knowledge, these findings from an exploratory analysis represent the first randomized data on continuous versus fixed-duration immunotherapy in previously treated advanced NSCLC and suggest that continuing nivolumab beyond 1 year improves outcomes. American Society of Clinical Oncology 2020-11-20 2020-09-10 /pmc/articles/PMC7676888/ /pubmed/32910710 http://dx.doi.org/10.1200/JCO.20.00131 Text en © 2020 by American Society of Clinical Oncology https://creativecommons.org/licenses/by-nc-nd/4.0/Creative Commons Attribution Non-Commercial No Derivatives 4.0 License: https://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | ORIGINAL REPORTS Waterhouse, David M. Garon, Edward B. Chandler, Jason McCleod, Michael Hussein, Maen Jotte, Robert Horn, Leora Daniel, Davey B. Keogh, George Creelan, Ben Einhorn, Lawrence H. Baker, Justin Kasbari, Samer Nikolinakos, Petros Babu, Sunil Couture, Felix Leighl, Natasha B. Reynolds, Craig Blumenschein, George Gunuganti, Vijay Li, Ang Aanur, Nivedita Spigel, David R. Continuous Versus 1-Year Fixed-Duration Nivolumab in Previously Treated Advanced Non–Small-Cell Lung Cancer: CheckMate 153 |
title | Continuous Versus 1-Year Fixed-Duration Nivolumab in Previously Treated Advanced Non–Small-Cell Lung Cancer: CheckMate 153 |
title_full | Continuous Versus 1-Year Fixed-Duration Nivolumab in Previously Treated Advanced Non–Small-Cell Lung Cancer: CheckMate 153 |
title_fullStr | Continuous Versus 1-Year Fixed-Duration Nivolumab in Previously Treated Advanced Non–Small-Cell Lung Cancer: CheckMate 153 |
title_full_unstemmed | Continuous Versus 1-Year Fixed-Duration Nivolumab in Previously Treated Advanced Non–Small-Cell Lung Cancer: CheckMate 153 |
title_short | Continuous Versus 1-Year Fixed-Duration Nivolumab in Previously Treated Advanced Non–Small-Cell Lung Cancer: CheckMate 153 |
title_sort | continuous versus 1-year fixed-duration nivolumab in previously treated advanced non–small-cell lung cancer: checkmate 153 |
topic | ORIGINAL REPORTS |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7676888/ https://www.ncbi.nlm.nih.gov/pubmed/32910710 http://dx.doi.org/10.1200/JCO.20.00131 |
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