Efficacy and Safety of Nivolumab Alone or in Combination With Ipilimumab in Patients With Mucosal Melanoma: A Pooled Analysis

被引:455
作者
D'Angelo, Sandra P. [1 ,2 ]
Larkin, James [3 ]
Sosman, Jeffrey A. [5 ]
Lebbe, Celeste [6 ]
Brady, Benjamin [8 ]
Neyns, Bart [9 ]
Schmidt, Henrik
Hassel, Jessica C. [10 ]
Hodi, F. Stephen [12 ]
Lorigan, Paul [4 ]
Savage, Kerry J. [13 ]
Miller, Wilson H., Jr. [14 ,15 ]
Mohr, Peter
Marquez-Rodas, Ivan [16 ]
Charles, Julie [7 ]
Kaatz, Martin [11 ]
Sznol, Mario [17 ,18 ]
Weber, Jeffrey S. [19 ]
Shoushtari, Alexander N. [1 ,2 ]
Ruisi, Mary [20 ]
Jiang, Joel [20 ]
Wolchok, Jedd D. [1 ,2 ]
机构
[1] Mem Sloan Kettering Canc Ctr, 300 East 66th St, New York, NY 10065 USA
[2] Weill Cornell Med Coll, New York, NY USA
[3] Royal Marsden Hosp, London, England
[4] Univ Manchester, Manchester, Lancs, England
[5] Vanderbilt Univ, Med Ctr, Nashville, TN USA
[6] Univ Paris Diderot, INSERM, U976, St Louis Hosp, Paris, France
[7] Grenoble Alps Univ, Grenoble Univ Hosp, Grenoble, France
[8] Cabrini Hlth, Melbourne, Vic, Australia
[9] Univ Ziekenhuis Brussel, Brussels, Belgium
[10] Univ Heidelberg Hosp, Heidelberg, Germany
[11] Univ Hosp Jena, SRH Waldklinikum Gera, Jena, Germany
[12] Dana Farber Canc Inst, Boston, MA 02115 USA
[13] Univ British Columbia, BC Canc Agcy, Vancouver, BC, Canada
[14] McGill Univ, Lady Davis Inst, Montreal, PQ, Canada
[15] McGill Univ, Jewish Gen Hosp, Montreal, PQ, Canada
[16] Hosp Gen Univ Gregorio Maranon, Madrid, Spain
[17] Yale Univ, Sch Med, New Haven, CT USA
[18] Yale New Haven Med Ctr, Smilow Canc Ctr, 20 York St, New Haven, CT 06504 USA
[19] H Lee Moffitt Canc Ctr & Res Inst, Tampa, FL USA
[20] Bristol Myers Squibb, Princeton, NJ USA
关键词
METASTATIC MELANOMA; UNTREATED MELANOMA; PRETREATED PATIENTS; CUTANEOUS MELANOMA; OPEN-LABEL; PHASE-II; CHEMOTHERAPY; MULTICENTER; SURVIVAL; TRIALS;
D O I
10.1200/JCO.2016.67.9258
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose Mucosal melanoma is an aggressive malignancy with a poor response to conventional therapies. The efficacy and safety of nivolumab (a programmed death-1 checkpoint inhibitor), alone or combined with ipilimumab (a cytotoxic T-lymphocyte antigen-4 checkpoint inhibitor), have not been reported in this rare melanoma subtype. Patients and Methods Data were pooled from 889 patients who received nivolumab monotherapy in clinical studies, including phase III trials; 86 (10%) had mucosal melanoma and 665 (75%) had cutaneous melanoma. Data were also pooled for patients who received nivolumab combined with ipilimumab (n = 35, mucosal melanoma; n = 326, cutaneous melanoma). Results Among patients who received nivolumab monotherapy, median progression-free survival was 3.0 months (95% CI, 2.2 to 5.4 months) and 6.2 months (95% CI, 5.1 to 7.5 months) for mucosal and cutaneous melanoma, with objective response rates of 23.3% (95% CI, 14.8% to 33.6%) and 40.9% (95% CI, 37.1% to 44.7%), respectively. Median progression-free survival in patients treated with nivolumab combined with ipilimumab was 5.9 months (95% CI, 2.8 months to not reached) and 11.7 months (95% CI, 8.9 to 16.7 months) for mucosal and cutaneous melanoma, with objective response rates of 37.1% (95% CI, 21.5% to 55.1%) and 60.4% (95% CI, 54.9% to 65.8%), respectively. For mucosal and cutaneous melanoma, respectively, the incidence of grade 3 or 4 treatment-related adverse events was 8.1% and 12.5% for nivolumab monotherapy and 40.0% and 54.9% for combination therapy. Conclusion To our knowledge, this is the largest analysis of data for anti-programmed death-1 therapy in mucosal melanoma to date. Nivolumab combined with ipilimumab seemed to have greater efficacy than either agent alone, and although the activity was lower in mucosal melanoma, the safety profile was similar between subtypes. (C) 2016 by American Society of Clinical Oncology
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页码:226 / +
页数:15
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