Nivolumab plus Cabozantinib versus Sunitinib for Advanced Renal-Cell Carcinoma

Toni K. Choueiri(Dana-Farber Cancer Institute), Thomas Powles(National Health Service), Mauricio Burotto, Bernard Escudier(Institut Gustave Roussy), María T. Bourlon(Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán), Bogdan Żurawski, Víctor Manuel Oyervides-Juárez(Hospital Universitario Dr José Eleuterio Gonzalez), James J. Hsieh(Washington University in St. Louis), Umberto Basso(Istituto Oncologico Veneto), Amishi Y. Shah(The University of Texas MD Anderson Cancer Center), Cristina Suárez(Vall d'Hebron Institute of Oncology), Alketa Hamzaj(Ospedale San Donato), Jeffrey C. Goh(Royal Brisbane and Women's Hospital), Carlos H. Barrios(Hospital São Lucas da PUCRS), Martin Eduardo Richardet(Instituto Oncológico de Córdoba), Camillo Porta(University of Pavia), Rubén Dario Kowalyszyn, Juan P. Feregrino(Instituto Tecnológico de Querétaro), Jakub Żołnierek, David Pook(Monash University), Elizabeth R. Kessler(University of Colorado Denver), Yoshihiko Tomita(Niigata University), Ryuichi Mizuno(Keio University), Jens Bedke(University of Tübingen), Joshua Zhang, Matthew Maurer, Burçin Şimşek(Cancer Research And Biostatistics), Flavia Ejzykowicz(Health Economics and Outcomes Research (United Kingdom)), Gisela Schwab(Exelixis (United States)), Andrea B. Apolo(Center for Cancer Research), Robert J. Motzer(Memorial Sloan Kettering Cancer Center)
New England Journal of Medicine
March 3, 2021
Cited by 1,722Open Access
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Abstract

BACKGROUND: The efficacy and safety of nivolumab plus cabozantinib as compared with those of sunitinib in the treatment of previously untreated advanced renal-cell carcinoma are not known. METHODS: In this phase 3, randomized, open-label trial, we randomly assigned adults with previously untreated clear-cell, advanced renal-cell carcinoma to receive either nivolumab (240 mg every 2 weeks) plus cabozantinib (40 mg once daily) or sunitinib (50 mg once daily for 4 weeks of each 6-week cycle). The primary end point was progression-free survival, as determined by blinded independent central review. Secondary end points included overall survival, objective response as determined by independent review, and safety. Health-related quality of life was an exploratory end point. RESULTS: Overall, 651 patients were assigned to receive nivolumab plus cabozantinib (323 patients) or sunitinib (328 patients). At a median follow-up of 18.1 months for overall survival, the median progression-free survival was 16.6 months (95% confidence interval [CI], 12.5 to 24.9) with nivolumab plus cabozantinib and 8.3 months (95% CI, 7.0 to 9.7) with sunitinib (hazard ratio for disease progression or death, 0.51; 95% CI, 0.41 to 0.64; P<0.001). The probability of overall survival at 12 months was 85.7% (95% CI, 81.3 to 89.1) with nivolumab plus cabozantinib and 75.6% (95% CI, 70.5 to 80.0) with sunitinib (hazard ratio for death, 0.60; 98.89% CI, 0.40 to 0.89; P = 0.001). An objective response occurred in 55.7% of the patients receiving nivolumab plus cabozantinib and in 27.1% of those receiving sunitinib (P<0.001). Efficacy benefits with nivolumab plus cabozantinib were consistent across subgroups. Adverse events of any cause of grade 3 or higher occurred in 75.3% of the 320 patients receiving nivolumab plus cabozantinib and in 70.6% of the 320 patients receiving sunitinib. Overall, 19.7% of the patients in the combination group discontinued at least one of the trial drugs owing to adverse events, and 5.6% discontinued both. Patients reported better health-related quality of life with nivolumab plus cabozantinib than with sunitinib. CONCLUSIONS: Nivolumab plus cabozantinib had significant benefits over sunitinib with respect to progression-free survival, overall survival, and likelihood of response in patients with previously untreated advanced renal-cell carcinoma. (Funded by Bristol Myers Squibb and others; CheckMate 9ER ClinicalTrials.gov number, NCT03141177.).


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