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| 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
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.
| 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 |
| 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) |
| 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). |