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

  • Lisa Zimmer
  • , Susmitha Apuri
  • , Zeynep Eroglu
  • , Lisa A. Kottschade
  • , Andrea Forschner
  • , Ralf Gutzmer
  • , Max Schlaak
  • , Lucie Heinzerling
  • , Angela M. Krackhardt
  • , Carmen Loquai
  • , Svetomir N. Markovic
  • , Richard W. Joseph
  • , Kelly Markey
  • , Jochen S. Utikal
  • , Carsten Weishaupt
  • , Simone M. Goldinger
  • , Vernon K. Sondak
  • , Jonathan S. Zager
  • , Dirk Schadendorf
  • , Nikhil I. Khushalani

Research output: Contribution to journalArticlepeer-review

160 Scopus citations

Abstract

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-naïve. 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-naïve patients.

Original languageEnglish
Pages (from-to)47-55
Number of pages9
JournalEuropean Journal of Cancer
Volume75
DOIs
StatePublished - 1 Apr 2017

Keywords

  • Anti-PD-1
  • Disease progression
  • Efficacy
  • Ipilimumab
  • Ipilimumab and nivolumab
  • Melanoma
  • Nivolumab
  • Pembrolizumab
  • Treatment failure

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