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| Indexado |
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| DOI | 10.1002/CNCR.34180 | ||||
| Año | 2022 | ||||
| Tipo | artículo de investigación |
Citas Totales
Autores Afiliación Chile
Instituciones Chile
% Participación
Internacional
Autores
Afiliación Extranjera
Instituciones
Extranjeras
Background Conditional survival estimates provide critical prognostic information for patients with advanced renal cell carcinoma (aRCC). Efficacy, safety, and conditional survival outcomes were assessed in CheckMate 214 (ClinicalTrials.gov identifier NCT02231749) with a minimum follow-up of 5 years. Methods Patients with untreated aRCC were randomized to receive nivolumab (NIVO) (3 mg/kg) plus ipilimumab (IPI) (1 mg/kg) every 3 weeks for 4 cycles, then either NIVO monotherapy or sunitinib (SUN) (50 mg) daily (four 6-week cycles). Efficacy was assessed in intent-to-treat, International Metastatic Renal Cell Carcinoma Database Consortium intermediate-risk/poor-risk, and favorable-risk populations. Conditional survival outcomes (the probability of remaining alive, progression free, or in response 2 years beyond a specified landmark) were analyzed. Results The median follow-up was 67.7 months; overall survival (median, 55.7 vs 38.4 months; hazard ratio, 0.72), progression-free survival (median, 12.3 vs 12.3 months; hazard ratio, 0.86), and objective response (39.3% vs 32.4%) benefits were maintained with NIVO+IPI versus SUN, respectively, in intent-to-treat patients (N = 550 vs 546). Point estimates for 2-year conditional overall survival beyond the 3-year landmark were higher with NIVO+IPI versus SUN (intent-to-treat patients, 81% vs 72%; intermediate-risk/poor-risk patients, 79% vs 72%; favorable-risk patients, 85% vs 72%). Conditional progression-free survival and response point estimates were also higher beyond 3 years with NIVO+IPI. Point estimates for conditional overall survival were higher or remained steady at each subsequent year of survival with NIVO+IPI in patients stratified by tumor programmed death ligand 1 expression, grade >= 3 immune-mediated adverse event experience, body mass index, and age. Conclusions Durable clinical benefits were observed with NIVO+IPI versus SUN at 5 years, the longest phase 3 follow-up for a first-line checkpoint inhibitor-based combination in patients with aRCC. Conditional estimates indicate that most patients who remained alive or in response with NIVO+IPI at 3 years remained so at 5 years.
| Ord. | Autor | Género | Institución - País |
|---|---|---|---|
| 1 | Motzer, Robert J. | Hombre |
Mem Sloan Kettering Canc Ctr - Estados Unidos
Memorial Sloan-Kettering Cancer Center - Estados Unidos |
| 2 | McDermott, D. F. | Hombre |
Beth Israel Deaconess Med Ctr - Estados Unidos
Dana-Farber/Harvard Cancer Center - Estados Unidos |
| 3 | Escudier, B. | Hombre |
Gustave Roussy - Francia
Institut de Cancerologie Gustave Roussy - Francia |
| 4 | BUROTTO-PICHUN, MAURICIO | Hombre |
Bradford Hill Clin Res Ctr - Chile
Bradford Hill Clinical Research Center - Chile |
| 5 | Choueiri, Toni K. | Hombre |
Harvard Med Sch - Estados Unidos
Harvard Medical School - Estados Unidos |
| 6 | Hammers, Hans J. | Hombre |
Univ Texas Southwestern Kidney Canc Program - Estados Unidos
UT Southwestern Medical Center - Estados Unidos |
| 7 | Barthélémy, P. | Hombre |
Strasbourg European Canc Inst - Francia
Medical Oncology - Francia |
| 8 | Plimack, E. | Mujer |
Fox Chase Canc Ctr - Estados Unidos
Fox Chase Cancer Center - Estados Unidos |
| 9 | Porta, Camillo | Hombre |
Univ Pavia - Italia
Univ Bari A Moro - Italia Università degli Studi di Pavia - Italia Università degli studi di Bari Aldo Moro - Italia |
| 10 | George, Saby | - |
Roswell Pk Canc Inst - Estados Unidos
Roswell Park Cancer Institute - Estados Unidos |
| 11 | Powles, Thomas | Hombre |
Queen Mary Univ London - Reino Unido
Barts and The London School of Medicine and Dentistry - Reino Unido |
| 12 | Donskov, F. | Hombre |
Aarhus Univ Hosp - Dinamarca
Aarhus Universitetshospital - Dinamarca |
| 13 | Gurney, Howard | Hombre |
Westmead Hosp - Australia
Macquarie Univ - Australia Westmead Hospital - Australia |
| 14 | Kollmannsberger, C. K. | Hombre |
British Columbia Canc Agcy - Canadá
British Columbia Cancer Agency - Canadá |
| 15 | Grimm, Marc-Oliver | Hombre |
Jena Univ Hosp - Alemania
Universitätsklinikum Jena und Medizinische Fakultät - Alemania |
| 16 | ESCOSTEGUY-BARRIOS, CARLOS HENRIQUE | Hombre |
Pontifica Universidade Católica do Rio Grande do Sul - Brasil
|
| 17 | Tomita, Y. | Hombre |
NIIGATA UNIV - Japón
Niigata University, Graduate School of Medical and Dental Science - Japón |
| 18 | Castellano, D. | Hombre |
October 12th Univ Hosp - España
Hospital Universitario 12 de Octubre - España |
| 19 | Gruenwald, Viktor | Hombre |
Univ Hosp Essen - Alemania
Universitätsklinikum Essen - Alemania |
| 20 | Rini, B. I. | Hombre |
Vanderbilt Univ - Estados Unidos
Vanderbilt University Medical Center - Estados Unidos |
| 21 | McHenry, M. B. | - |
Bristol Myers Squibb - Estados Unidos
Bristol-Myers Squibb - Estados Unidos |
| 22 | Lee, Chung Wei | - |
Bristol Myers Squibb - Estados Unidos
Bristol-Myers Squibb - Estados Unidos |
| 23 | McCarthy, Jennifer | Mujer |
Bristol Myers Squibb - Estados Unidos
Bristol-Myers Squibb - Estados Unidos |
| 24 | Ejzykowicz, Flavia | Mujer |
Bristol Myers Squibb - Estados Unidos
Bristol-Myers Squibb - Estados Unidos |
| 25 | Tannir, N. M. | Hombre |
Univ Texas MD Anderson Canc Ctr - Estados Unidos
University of Texas MD Anderson Cancer Center - Estados Unidos The University of Texas MD Anderson Cancer Center - Estados Unidos |
| Fuente |
|---|
| National Institutes of Health |
| Novartis |
| Ohio State University |
| GlaxoSmithKline |
| Bristol-Myers Squibb |
| National Cancer Institute |
| University of Pennsylvania |
| Eisai |
| Sanofi |
| Ono Pharmaceutical Company Limited |
| AbbVie |
| Gilead Sciences |
| Pfizer |
| AstraZeneca |
| ONO Pharmaceutical |
| Memorial Sloan Kettering Cancer Center Support Grant |
| Amgen |
| Boehringer Ingelheim |
| Johnson and Johnson |
| Merck |
| Harvard Medical School |
| Eli Lilly and Company |
| EMD Serono |
| Merck KGaA |
| Roche |
| Takeda Pharmaceuticals U.S.A. |
| Janssen Pharmaceuticals |
| Merck Sharp and Dohme |
| Corvus Pharmaceuticals |
| Peloton Therapeutics |
| Asana BioSciences |
| EUSA Pharma |
| AB Science |
| University of Texas MD Anderson Cancer Center |
| Bristol Myers Squibb |
| MSD Oncology |
| General Electric |
| Astellas Pharma US |
| American Society of Clinical Oncology |
| European Society for Medical Oncology |
| National Comprehensive Cancer Network |
| Georgetown University |
| Ipsen Biopharmaceuticals |
| Nihon Pharmaceutical |
| Shionogi |
| Janssen Oncology |
| Jounce Therapeutics |
| BioCryst |
| Bayer Fund |
| Curio Science |
| Canadian Urological Association |
| Abraxis Biosciences |
| Anika Therapeutics |
| Society for Immunotherapy of Cancer |
| Shanghai Henlius Biotech |
| Vanguard Health Care ETF |
| NAMC |
| ACHL |
| First Trust Amex Biotech |
| Dana-Farber/Harvard Specialized Program of Research Excellence |
| Synthekine Inc |
| Exelixis Inc |
| GU ASCO |
| American Society of Clinical Oncology Genitourinary Cancers Symposium |
| Zodiac Pharma |
| Aptitude Health |
| Werewolf Therapeutics |
| Deutsche Gesellschaft für Urologie |
| Agradecimiento |
|---|
| This study was sponsored by Bristol Myers Squibb and Ono Pharmaceutical Company Limited. The University of Texas MD Anderson Cancer Center is supported by the National Institutes of Health (grant P30 CA016672). Patients treated at Memorial Sloan Kettering Cancer Center were supported in part by the Memorial Sloan Kettering Cancer Center Support Grant (core grant P30 CA008748). |
| We thank the patients who participated in this study, the clinical study teams, and the representatives of the sponsor who were involved in data collection and analyses. Medical writing support was provided by Rachel Maddente, PhD, of Parexel, and was funded by Bristol Myers Squibb. |