Nivolumab Plus Ipilimumab in Patients With Advanced Melanoma: Updated Survival, Response, and Safety Data in a Phase I Dose-Escalation Study

被引:142
|
作者
Callahan, Margaret K. [1 ,2 ]
Kluger, Harriet [3 ,4 ,5 ]
Postow, Michael A. [1 ,2 ]
Segal, Neil H. [1 ,2 ]
Lesokhin, Alexander [1 ,2 ]
Atkins, Michael B. [6 ]
Kirkwood, John M. [7 ]
Krishnan, Suba [8 ]
Bhore, Rafia [8 ]
Horak, Christine [8 ]
Wolchok, Jedd D. [1 ,2 ]
Sznol, Mario [3 ,4 ,5 ]
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] Yale Univ, Sch Med, New Haven, CT USA
[4] Smilow Canc Ctr, New Haven, CT USA
[5] Yale New Haven Med Ctr, 20 York St, New Haven, CT 06504 USA
[6] Georgetown Lombardi Comprehens Canc Ctr, Washington, DC USA
[7] Univ Pittsburgh, Med Ctr, Pittsburgh, PA USA
[8] Bristol Myers Squibb Co, Princeton, NJ USA
关键词
UNTREATED MELANOMA; PEMBROLIZUMAB; MONOTHERAPY; TRAMETINIB; DABRAFENIB;
D O I
10.1200/JCO.2017.72.2850
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Purpose The clinical activity observed in a phase I dose-escalation study of concurrent therapy with nivolumab (NIVO) and ipilimumab (IPI) in patients with previously treated or untreated advanced melanoma led to subsequent clinical development, including randomized trials. Here, we report long-term follow-up data from study CA209-004, including 3-year overall survival (OS). Patients and Methods Concurrent cohorts 1, 2, 2a, and 3 received escalating doses of NIVO plus IPI once every 3 weeks for four doses, followed by NIVO once every 3 weeks for four doses, then NIVO plus IPI once every 12 weeks for eight doses. An expansion cohort (cohort 8) received concurrent NIVO 1 mg/kg plus IPI 3 mg/kg once every 3 weeks for four doses, followed by NIVO 3 mg/kg once every 2 weeks, which is the dose and schedule used in phase II and III studies and now approved for patients with unresectable or metastatic melanoma. Results Among all concurrent cohorts (N = 94) at a follow-up of 30.3 to 55.0 months, the 3-year OS rate was 63% and median OS had not been reached. Objective response rate by modified WHO criteria was 42%, and median duration of response was 22.3 months. Incidence of grade 3 and 4 treatment-trelated adverse events was 59%. The most common grade 3 and 4 treatment-related adverse events were increases in lipase (15%), alanine aminotransferase (12%), and aspartate aminotransferase (11%). One treatment-related death (1.1%) occurred in a patient who had multiorgan failure 70 days after the last dose of NIVO plus IPI. Conclusion This is the longest follow-up for NIVO plus IPI combination therapy in patients with advanced melanoma. The 3-year OS rate of 63% is the highest observed for this patient population and provides additional evidence for the durable clinical activity of immune checkpoint inhibitors in the treatment of advanced melanoma. (C) 2017 by American Society of Clinical Oncology
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收藏
页码:391 / +
页数:14
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