Nivolumab plus cabozantinib versus sunitinib for advanced renal-cell carcinoma Journal Article


Authors: Choueiri, T. K.; Powles, T.; Burotto, M.; Escudier, B.; Bourlon, M. T.; Zurawski, B.; Oyervides Juárez, V. M.; Hsieh, J. J.; Basso, U.; Shah, A. Y.; Suárez, C.; Hamzaj, A.; Goh, J. C.; Barrios, C.; Richardet, M.; Porta, C.; Kowalyszyn, R.; Feregrino, J. P.; Zołnierek, J.; Pook, D.; Kessler, E. R.; Tomita, Y.; Mizuno, R.; Bedke, J.; Zhang, J.; Maurer, M. A.; Simsek, B.; Ejzykowicz, F.; Schwab, G. M.; Apolo, A. B.; Motzer, R. J.; for the CheckMate 9ER Investigators
Article Title: Nivolumab plus cabozantinib versus sunitinib for advanced renal-cell carcinoma
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.). Copyright © 2021 Massachusetts Medical Society.
Keywords: adult; controlled study; treatment response; aged; aged, 80 and over; middle aged; survival analysis; major clinical study; overall survival; clinical trial; constipation; fatigue; mortality; sunitinib; advanced cancer; cancer growth; diarrhea; drug efficacy; drug safety; drug withdrawal; hypertension; hypophosphatemia; treatment duration; antineoplastic agents; pyridines; comparative study; follow up; antineoplastic agent; cancer grading; progression free survival; quality of life; multiple cycle treatment; anemia; mucosa inflammation; nausea; randomized controlled trial; stomatitis; vomiting; antineoplastic combined chemotherapy protocols; proportional hazards models; protein tyrosine kinase; renal cell carcinoma; kidney neoplasms; cancer mortality; abdominal pain; arthralgia; asthenia; backache; coughing; fever; hypomagnesemia; pruritus; rash; hyponatremia; proportional hazards model; kidney tumor; carcinoma, renal cell; multicenter study; peripheral edema; liver disease; open study; headache; phase 3 clinical trial; receptor protein-tyrosine kinases; hypothyroidism; hand foot syndrome; muscle spasm; proteinuria; anilides; upper respiratory tract infection; dysgeusia; pyridine derivative; anilide; programmed death 1 ligand 1; progression-free survival; decreased appetite; dysphonia; cabozantinib; body weight disorder; nivolumab; very elderly; intention to treat analysis; humans; human; male; female; priority journal; article; cd274 protein, human; b7-h1 antigen
Journal Title: New England Journal of Medicine
Volume: 384
Issue: 9
ISSN: 0028-4793
Publisher: Massachusetts Medical Society  
Date Published: 2021-03-04
Start Page: 829
End Page: 841
Language: English
DOI: 10.1056/NEJMoa2026982
PUBMED: 33657295
PROVIDER: scopus
PMCID: PMC8436591
DOI/URL:
Notes: Article -- Export Date: 1 April 2021 -- Source: Scopus
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  1. Robert Motzer
    1247 Motzer