Overall Survival with Combined Nivolumab and Ipilimumab in Advanced Melanoma

被引:2815
作者
Wolchok, J. D. [1 ,2 ]
Chiarion-Sileni, V. [3 ]
Gonzalez, R. [8 ]
Rutkowski, P. [9 ]
Grob, J. -J. [10 ]
Cowey, C. L. [12 ]
Lao, C. D. [13 ]
Wagstaff, J. [14 ]
Schadendorf, D. [16 ,17 ]
Ferrucci, P. F. [4 ]
Smylie, M. [18 ]
Dummer, R. [20 ]
Hill, A. [21 ]
Hogg, D. [19 ]
Haanen, J. [27 ]
Carlino, M. S. [22 ]
Bechter, O. [28 ]
Maio, M. [5 ]
Marquez-Rodas, I. [29 ]
Guidoboni, M. [6 ]
McArthur, G. [25 ]
Lebbe, C. [11 ]
Ascierto, P. A. [7 ]
Long, G. V. [23 ,24 ]
Cebon, J. [26 ]
Sosman, J. [30 ]
Postow, M. A. [1 ,2 ]
Callahan, M. K. [1 ,2 ]
Walker, D. [31 ]
Rollin, L. [31 ]
Bhore, R. [31 ]
Hodi, F. S. [32 ]
Larkin, J. [15 ]
机构
[1] Mem Sloan Kettering Canc Ctr, 1275 York Ave, New York, NY 10021 USA
[2] Weill Cornell Med Coll, New York, NY USA
[3] IRCCS, Oncol Inst Veneto, Padua, Italy
[4] European Inst Oncol, Milan, Italy
[5] Univ Hosp Siena, Ctr Immunooncol, Ist Toscano Tumori, Siena, Italy
[6] IRCCS, Ist Sci Romagnolo Studio Cura Tumori, Immunotherapy & Somat Cell Therapy Unit, Meldola, Italy
[7] Fdn Pascale, Ist Nazl Tumori, Naples, Italy
[8] Univ Colorado, Denver, CO 80202 USA
[9] Oncol Ctr, Maria Sklodowska Curie Inst, Warsaw, Poland
[10] Aix Marseille Univ, Hop Timone, Marseille, France
[11] Univ Paris Diderot, Hop St Louis, AP HP, Dermatol & Ctr Invest Clin,INSERM Unite 976, Paris, France
[12] Baylor Canc Ctr, Texas Oncol, Dallas, TX USA
[13] Univ Michigan, Ann Arbor, MI 48109 USA
[14] Swansea Univ, Coll Med, Swansea, W Glam, Wales
[15] Royal Marsden NHS Fdn Trust, London, England
[16] Univ Essen Gesamthsch, Dept Dermatol, Essen, Germany
[17] German Canc Consortium, Heidelberg, Germany
[18] Cross Canc Inst, Edmonton, AB, Canada
[19] Princess Margaret Canc Ctr, Toronto, ON, Canada
[20] Univ Spital, Zurich, Switzerland
[21] Tasman Oncol Res, Southport Gold Coast, Qld, Australia
[22] Univ Sydney, Melanoma Inst Australia, Crown Princess Mary Canc Ctr, Sydney, NSW, Australia
[23] Univ Sydney, Melanoma Inst Australia, Sydney, NSW, Australia
[24] Royal North Shore & Mater Hosp, Sydney, NSW, Australia
[25] Univ Melbourne, Peter MacCallum Canc Ctr, Melbourne, Vic, Australia
[26] Univ Melbourne, Oliivia Newton John Canc Res Inst, Melbourne, Vic, Australia
[27] Netherlands Canc Inst, Amsterdam, Netherlands
[28] Katholieke Univ Leuven, Univ Hosp Leuven, Leuven, Belgium
[29] Gen Univ Hosp Gregorio Maranon, Madrid, Spain
[30] Northwestern Univ, Chicago, IL 60611 USA
[31] Bristol Myers Squibb, Princeton, NJ USA
[32] Dana Farber Canc Inst, Boston, MA 02115 USA
关键词
METASTATIC MELANOMA; UNTREATED MELANOMA;
D O I
10.1056/NEJMoa1709684
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:1345 / 1356
页数:12
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