Ipilimumab alone or in combination with nivolumab after progression on anti-PD-1 therapy in advanced melanoma

被引:133
|
作者
Zimmer, Lisa [1 ,2 ]
Apuri, Susmitha [3 ]
Eroglu, Zeynep [4 ]
Kottschade, Lisa A. [5 ]
Forschner, Andrea [6 ]
Gutzmer, Ralf [7 ]
Schlaak, Max [8 ]
Heinzerling, Lucie [9 ]
Krackhardt, Angela M. [10 ]
Loquai, Carmen [11 ]
Markovic, Svetomir N. [5 ]
Joseph, Richard W. [5 ]
Markey, Kelly [4 ]
Utikal, Jochen S. [12 ,13 ]
Weishaupt, Carsten [14 ]
Goldinger, Simone M. [15 ]
Sondak, Vernon K. [4 ]
Zager, Jonathan S. [4 ]
Schadendorf, Dirk [1 ,2 ]
Khushalani, Nikhil I. [4 ]
机构
[1] Univ Duisburg Essen, Univ Hosp, Dept Dermatol, Essen, Germany
[2] German Canc Consortium DKTK, Heidelberg, Germany
[3] Univ S Florida, H Lee Moffitt Canc Ctr & Res Inst, Hematol Oncol Fellowship Program, Tampa, FL USA
[4] H Lee Moffitt Canc Ctr & Res Inst, Dept Cutaneous Oncol, Tampa, FL USA
[5] Mayo Clin, Dept Oncol Hematol & Immunol, Rochester, MN USA
[6] Univ Hosp Tubingen, Dept Dermatol, Tubingen, Germany
[7] Hannover Med Sch, Dept Dermatol & Allergy, Skin Canc Ctr Hannover, Hannover, Germany
[8] Univ Hosp Cologne, Dept Dermatol, Skin Canc Ctr, Ctr Integrated Oncol CIO Koln, Bonn, Germany
[9] Friedrich Alexander Univ Erlangen Nurnberg FAU, Univ Hosp Erlangen, Dept Dermatol, Erlangen, Germany
[10] Tech Univ Muchen TUM Munich, Dept Med 3, Munich, Germany
[11] Univ Hosp Mainz, Dept Dermatol, Mainz, Germany
[12] German Canc Res Ctr, Skin Canc Unit, Heidelberg, Germany
[13] Ruprecht Karl Univ Heidelberg, Univ Med Ctr Mannheim, Dept Dermatol Venereol & Allergol, Mannheim, Germany
[14] Univ Hosp Munster, Dept Dermatol, Munster, Germany
[15] Univ Hosp Zurich, Dept Dermatol, Zurich, Switzerland
关键词
Nivolumab; Pembrolizumab; Treatment failure; Efficacy; Ipilimumab; Ipilimumab and nivolumab; Melanoma; Disease progression; Anti-PD-1; METASTATIC MELANOMA; UNTREATED MELANOMA; PD-1; BLOCKADE; PEMBROLIZUMAB; TRIAL; CHEMOTHERAPY; RESISTANCE;
D O I
10.1016/j.ejca.2017.01.009
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: The anti-programmed cell death-1 (PD-1) inhibitors pembrolizumab and nivolumab alone or in combination with ipilimumab have shown improved objective response rates and progression-free survival compared to ipilimumab only in advanced melanoma patients. Anti-PD-1 therapy demonstrated nearly equal clinical efficacy in patients who had progressed after ipilimumab or were treatment-naive. However, only limited evidence exists regarding the efficacy of ipilimumab alone or in combination with nivolumab after treatment failure to anti-PD-therapy. Patients and methods: A multicenter retrospective study in advanced melanoma patients who were treated with nivolumab (1 or 3 mg/kg) and ipilimumab (1 mg or 3 mg/kg) or ipilimumab (3 mg/kg) alone after treatment failure to anti-PD-1 therapy was performed. Patient, tumour, pre- and post-treatment characteristics were analysed. Results: In total, 47 patients were treated with ipilimumab (ipi-group) and 37 patients with ipilimumab and nivolumab (combination-group) after treatment failure to anti-PD-1 therapy. Overall response rates for the ipi- and the combination-group were 16% and 21%, respectively. Disease control rate was 42% for the ipi-group and 33% for the combination-group. One-year overall survival rates for the ipi- and the combination-group were 54% and 55%, respectively. Conclusions: Ipilimumab should be considered as a viable treatment option for patients with failure to prior anti-PD-1 therapy, including those with progressive disease as best response to prior anti-PD-1. In contrast, the combination of ipilimumab and nivolumab appears significantly less effective in this setting compared to treatment-naive patients. (C) 2017 Elsevier Ltd. All rights reserved.
引用
收藏
页码:47 / 55
页数:9
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