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Departamento Gestión de Conocimiento, Monitoreo y Prospección
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Conditional survival and long-term efficacy with nivolumab plus ipilimumab versus sunitinib in patients with advanced renal cell carcinoma
Indexado
WoS WOS:000778109800001
Scopus SCOPUS_ID:85127785977
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


Abstract



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.

Revista



Revista ISSN
Cancer 0008-543X

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Disciplinas de Investigación



WOS
Oncology
Scopus
Sin Disciplinas
SciELO
Sin Disciplinas

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Publicaciones WoS (Ediciones: ISSHP, ISTP, AHCI, SSCI, SCI), Scopus, SciELO Chile.

Colaboración Institucional



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Autores - Afiliación



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

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Financiamiento



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

Muestra la fuente de financiamiento declarada en la publicación.

Agradecimientos



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.

Muestra la fuente de financiamiento declarada en la publicación.