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First-line Nivolumab plus Ipilimumab Versus Sunitinib in Patients Without Nephrectomy and With an Evaluable Primary Renal Tumor in the CheckMate 214 Trial
Indexado
WoS WOS:000809752100016
Scopus SCOPUS_ID:85118750007
DOI 10.1016/J.EURURO.2021.10.001
Año 2022
Tipo artículo de investigación

Citas Totales

Autores Afiliación Chile

Instituciones Chile

% Participación
Internacional

Autores
Afiliación Extranjera

Instituciones
Extranjeras


Abstract



We present an exploratory post hoc analysis from the phase 3 CheckMate 214 trial of first-line nivolumab plus ipilimumab (NIVO+IPI) versus sunitinib in a subgroup of 108 patients with advanced renal cell carcinoma (aRCC) without prior nephrectomy and with an evaluable primary tumor, a population under-represented in clinical trials. Patients with clear cell aRCC were randomized to NIVO+IPI every 3 wk for four doses followed by NIVO monotherapy, or sunitinib every day for 4 wk (6-wk cycle). Overall survival (OS), progression-free survival (PFS), objective response rate (ORR), and primary tumor shrinkage were assessed. PFS and ORR were assessed per independent radiology review committee using RECIST version 1.1. With minimum study follow-up of 4 yr for intent-to-treat patients, OS favored NIVO+IPI (n = 53) over sunitinib (n = 55; hazard ratio 0.63, 95% confidence interval 0.40–1.0) among patients without prior nephrectomy. ORR was higher (34% vs 15%; p = 0.0041) and median duration of response was longer with NIVO+IPI versus sunitinib (20.5 vs 14.1 mo); the best overall response was partial response in either arm. A ≥30% reduction in the diameter of intact target renal tumors was achieved in 35% of patients with NIVO+IPI versus 20% with sunitinib. Safety was consistent with the global study population. In conclusion, in patients with aRCC without prior nephrectomy and with an evaluable primary tumor, NIVO+IPI showed survival benefits and renal tumor reduction versus sunitinib. This trial is registered at ClinicalTrials.gov as NCT02231749. Patient summary: In an exploratory analysis of a large global trial (CheckMate 214), we observed positive outcomes (both survival and tumor response to treatment) with nivolumab plus ipilimumab over sunitinib in a subgroup of patients with advanced kidney cancer who did not undergo removal of their primary kidney tumor. This subset of patients represents a population that has not been studied in clinical trials and for whom outcomes with new immunotherapy combination regimens are not yet known. We conclude that treatment with nivolumab plus ipilimumab offers these patients a survival benefit versus sunitinib, consistent with that observed in the overall study, as well as a notable kidney tumor reduction.

Revista



Revista ISSN
European Urology 0302-2838

Métricas Externas



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Disciplinas de Investigación



WOS
Urology & Nephrology
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 Albiges, Laurence Mujer Institut de Cancerologie Gustave Roussy - Francia
Gustave Roussy - Francia
2 Tannir, N. M. Hombre University of Texas MD Anderson Cancer Center - Estados Unidos
Univ Texas MD Anderson Canc Ctr - Estados Unidos
The University of Texas MD Anderson Cancer Center - Estados Unidos
3 BUROTTO-PICHUN, MAURICIO Hombre Bradford Hill Clinical Research Center - Chile
Bradford Hill Clin Res Ctr - Chile
4 McDermott, David Hombre Dana-Farber/Harvard Cancer Center - Estados Unidos
Beth Israel Deaconess Med Ctr - Estados Unidos
5 Plimack, E. Mujer Fox Chase Cancer Center - Estados Unidos
Fox Chase Canc Ctr - Estados Unidos
6 Barthélémy, P. Hombre Medical Oncology - Francia
Inst Cancerol Strasbourg Europe - Francia
7 Porta, Camillo Hombre Università degli Studi di Pavia - Italia
Univ Pavia - Italia
8 Powles, Thomas Hombre Barts and The London School of Medicine and Dentistry - Reino Unido
Queen Mary Univ London - Reino Unido
9 Donskov, F. Hombre Aarhus Universitetshospital - Dinamarca
Aarhus Univ Hosp - Dinamarca
10 George, Saby - Roswell Park Cancer Institute - Estados Unidos
Roswell Park Canc Inst - Estados Unidos
11 Kollmannsberger, C. K. Hombre British Columbia Cancer Agency - Canadá
British Columbia Canc Agcy - Canadá
12 Gurney, Howard Hombre Westmead Hospital - Australia
Westmead Hosp - Australia
Macquarie Univ - Australia
13 Grimm, Marc-Oliver Hombre Universitätsklinikum Jena und Medizinische Fakultät - Alemania
Jena Univ Hosp - Alemania
14 Tomita, Y. Hombre Niigata University, Graduate School of Medical and Dental Science - Japón
NIIGATA UNIV - Japón
15 Castellano, D. Hombre Hospital Universitario - España
Hosp Univ 12 Octubre - España
Hospital Universitario 12 de Octubre - España
16 Rini, B. I. Hombre Vanderbilt University Medical Center - Estados Unidos
Vanderbilt Univ - Estados Unidos
17 Choueiri, Toni K. Hombre Brigham and Women's Hospital - Estados Unidos
Brigham & Womens Hosp - Estados Unidos
Harvard Med Sch - Estados Unidos
18 Leung, David Hombre Bristol-Myers Squibb - Estados Unidos
Dept Imaging - Estados Unidos
Bristol Myers Squibb - Estados Unidos
19 Saggi, Shruti Shally Mujer Bristol-Myers Squibb - Estados Unidos
Bristol Myers Squibb - Estados Unidos
20 Lee, Chung Wei - Bristol-Myers Squibb - Estados Unidos
Bristol Myers Squibb - Estados Unidos
21 McHenry, M. B. - Bristol-Myers Squibb - Estados Unidos
Bristol Myers Squibb - Estados Unidos
22 Motzer, Robert J. Hombre Memorial Sloan-Kettering Cancer Center - Estados Unidos
Mem Sloan Kettering Canc Ctr - Estados Unidos

Muestra la afiliación y género (detectado) para los co-autores de la publicación.

Financiamiento



Fuente
National Institutes of Health
Novartis
Bristol-Myers Squibb
National Cancer Institute
Eisai
Bayer
Pfizer
AstraZeneca
ONO Pharmaceutical
Memorial Sloan Kettering Cancer Center Support Grant
Meso Scale Diagnostics
Boehringer Ingelheim
Johnson and Johnson
Merck
Eli Lilly and Company
Genentech
EMD Serono
Calithera Biosciences
Roche
Astellas Pharma
Sanofi Genzyme
Ipsen
Prometheus Laboratories
Intuitive Surgical
Corvus Pharmaceuticals
Peloton Therapeutics
Exelixis
Takeda Pharmaceutical Company
Astellas Pharma US
American Society of Clinical Oncology
European Society for Medical Oncology
National Comprehensive Cancer Network
Nektar Therapeutics
Alexion Pharmaceuticals
Janssen Oncology
Lilly Oncology
QED Therapeutics
Bristol Myers Squibb (Princeton, NJ)
Sanofi/Aventis
Ono Pharmaceutical Company
UpToDate
Michael J. Hennessy Associates
Neolukin Therapeutics
Arrowhead Pharmaceuticals
3D Medicines
Ono Pharmaceutical Company (Osaka, Japan)

Muestra la fuente de financiamiento declarada en la publicación.

Agradecimientos



Agradecimiento
Funding/Support and role of the sponsor: This work was supported by Bristol Myers Squibb (Princeton, NJ) and Ono Pharmaceutical Company (Osaka, Japan). Authors received no financial support or compensation for publication of this manuscript. 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 Memorial Sloan Kettering Cancer Center Support Grant (Core Grant, number P30 CA008748).
Funding/Support and role of the sponsor: This work was supported by Bristol Myers Squibb (Princeton, NJ) and Ono Pharmaceutical Company (Osaka, Japan). Authors received no financial support or compensation for publication of this manuscript. 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 Memorial Sloan Kettering Cancer Center Support Grant (Core Grant, number P30 CA008748).
This work was supported by Bristol Myers Squibb (Princeton, NJ) and Ono Pharmaceutical Company (Osaka, Japan). Authors received no financial support or compensation for publication of this manuscript. 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 Memorial Sloan Kettering Cancer Center Support Grant (Core Grant, number P30 CA008748).

Muestra la fuente de financiamiento declarada en la publicación.