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Conditional survival and long-term efficacy with nivolumab plus ipilimumab versus sunitinib in patients with advanced renal cell carcinoma.
Motzer, Robert J; McDermott, David F; Escudier, Bernard; Burotto, Mauricio; Choueiri, Toni K; Hammers, Hans J; Barthélémy, Philippe; Plimack, Elizabeth R; Porta, Camillo; George, Saby; Powles, Thomas; Donskov, Frede; Gurney, Howard; Kollmannsberger, Christian K; Grimm, Marc-Oliver; Barrios, Carlos; Tomita, Yoshihiko; Castellano, Daniel; Grünwald, Viktor; Rini, Brian I; McHenry, M Brent; Lee, Chung-Wei; McCarthy, Jennifer; Ejzykowicz, Flavia; Tannir, Nizar M.
Afiliación
  • Motzer RJ; Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, New York.
  • McDermott DF; Division of Medical Oncology, Beth Israel Deaconess Medical Center, Dana-Farber/Harvard Cancer Center, Boston, Massachusetts.
  • Escudier B; Department of Medical Oncology, Gustave Roussy, Villejuif, France.
  • Burotto M; Bradford Hill Clinical Research Center, Santiago, Chile.
  • Choueiri TK; Department of Medical Oncology, Lank Center for Genitourinary Oncology, Dana-Farber Cancer Institute, Brigham and Women's Hospital, and Harvard Medical School, Boston, Massachusetts.
  • Hammers HJ; Department of Medical Oncology, University of Texas Southwestern Kidney Cancer Program, Dallas, Texas.
  • Barthélémy P; Medical Oncology, Strasbourg European Cancer Institute, Strasbourg, France.
  • Plimack ER; Department of Hematology and Oncology, Fox Chase Cancer Center, Philadelphia, Pennsylvania.
  • Porta C; Department of Internal Medicine, University of Pavia, Pavia, Italy.
  • George S; Department of Medicine, Roswell Park Cancer Institute, Buffalo, New York.
  • Powles T; Department of Genitourinary Oncology, Barts Cancer Institute, Cancer Research UK Experimental Cancer Medicine Center, Queen Mary University of London, Royal Free National Health Service Trust, London, United Kingdom.
  • Donskov F; Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.
  • Gurney H; Department of Medical Oncology, Westmead Hospital and Macquarie University, Sydney, New South Wales, Australia.
  • Kollmannsberger CK; Department of Medicine, British Columbia Cancer Agency, Vancouver, British Columbia, Canada.
  • Grimm MO; Department of Urology, Jena University Hospital, Jena, Germany.
  • Barrios C; Oncology Research Unit, Saint Luke Hospital, Pontifical Catholic University of Rio Grande do Sul, Porto Alegre, Brazil.
  • Tomita Y; Departments of Urology and Molecular Oncology, Niigata University Graduate School of Medical and Dental Sciences, Niigata, Japan.
  • Castellano D; Medical Oncology Department, October 12th University Hospital, Cancer Network Biomedical Research Center, Madrid, Spain.
  • Grünwald V; Interdisciplinary Genitourinary Oncology, West German Cancer Center Clinic for Internal Medicine and Clinic for Urology, University Hospital Essen, Essen, Germany.
  • Rini BI; Division of Hematology and Oncology, Vanderbilt University Medical Center, Nashville, Tennessee.
  • McHenry MB; Department of Biostatistics, Bristol Myers Squibb, Princeton, New Jersey.
  • Lee CW; Department of Clinical Trials, Bristol Myers Squibb, Princeton, New Jersey.
  • McCarthy J; Department of Clinical Scientists, Bristol Myers Squibb, Princeton, New Jersey.
  • Ejzykowicz F; Department of Health Economics and Outcomes Research, Bristol Myers Squibb, Princeton, New Jersey.
  • Tannir NM; Department of Genitourinary Medical Oncology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Cancer ; 128(11): 2085-2097, 2022 06 01.
Article en En | MEDLINE | ID: mdl-35383908
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.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 6_ODS3_enfermedades_notrasmisibles Problema de salud: 6_kidney_renal_pelvis_ureter_cancer Asunto principal: Carcinoma de Células Renales / Neoplasias Renales Tipo de estudio: Clinical_trials Límite: Female / Humans / Male Idioma: En Revista: Cancer Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Contexto en salud: 6_ODS3_enfermedades_notrasmisibles Problema de salud: 6_kidney_renal_pelvis_ureter_cancer Asunto principal: Carcinoma de Células Renales / Neoplasias Renales Tipo de estudio: Clinical_trials Límite: Female / Humans / Male Idioma: En Revista: Cancer Año: 2022 Tipo del documento: Article
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