Overall Survival with Combined Nivolumab and Ipilimumab in Advanced Melanoma

Jedd D. Wolchok(Memorial Sloan Kettering Cancer Center), Vanna Chiarion‐Sileni(University of Padua), René González(Cornell University), Piotr Rutkowski(Cornell University), Jean‐Jacques Grob(Cornell University), C. Lance Cowey(Cornell University), Christopher D. Lao(Cornell University), John Wagstaff(Cornell University), Dirk Schadendorf(German Cancer Research Center), Pier Francesco Ferrucci(Cornell University), Michael Smylie(Cornell University), Reinhard Dummer(Cornell University), Andrew Hill(Cornell University), David Hogg(Cornell University), John B.A.G. Haanen(Cornell University), Matteo S. Carlino(The University of Sydney), Oliver Bechter(Cornell University), Michele Maio(University of Siena), Iván Márquez‐Rodas(Cornell University), Massimo Guidoboni(Cornell University), Grant A. McArthur(Cornell University), Célèste Lebbé(Inserm), Paolo A. Ascierto(Cornell University), Georgina V. Long(Cornell University), Jonathan Cebon(The University of Melbourne), Jeffrey A. Sosman(Cornell University), Michael A. Postow(Memorial Sloan Kettering Cancer Center), Margaret K. Callahan(Memorial Sloan Kettering Cancer Center), Dana Walker(Cornell University), Linda Rollin(Cornell University), Rafia Bhore(Cornell University), F. Stephen Hodi(Cornell University), James Larkin(Royal Marsden NHS Foundation Trust)
New England Journal of Medicine
September 11, 2017
Cited by 5,379Open Access
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Abstract

BACKGROUND: Nivolumab combined with ipilimumab resulted in longer progression-free survival and a higher objective response rate than ipilimumab alone in a phase 3 trial involving patients with advanced melanoma. We now report 3-year overall survival outcomes in this trial. METHODS: We randomly assigned, in a 1:1:1 ratio, patients with previously untreated advanced melanoma to receive nivolumab at a dose of 1 mg per kilogram of body weight plus ipilimumab at a dose of 3 mg per kilogram every 3 weeks for four doses, followed by nivolumab at a dose of 3 mg per kilogram every 2 weeks; nivolumab at a dose of 3 mg per kilogram every 2 weeks plus placebo; or ipilimumab at a dose of 3 mg per kilogram every 3 weeks for four doses plus placebo, until progression, the occurrence of unacceptable toxic effects, or withdrawal of consent. Randomization was stratified according to programmed death ligand 1 (PD-L1) status, BRAF mutation status, and metastasis stage. The two primary end points were progression-free survival and overall survival in the nivolumab-plus-ipilimumab group and in the nivolumab group versus the ipilimumab group. RESULTS: At a minimum follow-up of 36 months, the median overall survival had not been reached in the nivolumab-plus-ipilimumab group and was 37.6 months in the nivolumab group, as compared with 19.9 months in the ipilimumab group (hazard ratio for death with nivolumab plus ipilimumab vs. ipilimumab, 0.55 [P<0.001]; hazard ratio for death with nivolumab vs. ipilimumab, 0.65 [P<0.001]). The overall survival rate at 3 years was 58% in the nivolumab-plus-ipilimumab group and 52% in the nivolumab group, as compared with 34% in the ipilimumab group. The safety profile was unchanged from the initial report. Treatment-related adverse events of grade 3 or 4 occurred in 59% of the patients in the nivolumab-plus-ipilimumab group, in 21% of those in the nivolumab group, and in 28% of those in the ipilimumab group. CONCLUSIONS: Among patients with advanced melanoma, significantly longer overall survival occurred with combination therapy with nivolumab plus ipilimumab or with nivolumab alone than with ipilimumab alone. (Funded by Bristol-Myers Squibb and others; CheckMate 067 ClinicalTrials.gov number, NCT01844505 .).


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