| Literature DB >> 28841387 |
Dirk Schadendorf1, Jedd D Wolchok1, F Stephen Hodi1, Vanna Chiarion-Sileni1, Rene Gonzalez1, Piotr Rutkowski1, Jean-Jacques Grob1, C Lance Cowey1, Christopher D Lao1, Jason Chesney1, Caroline Robert1, Kenneth Grossmann1, David McDermott1, Dana Walker1, Rafia Bhore1, James Larkin1, Michael A Postow1.
Abstract
Purpose Approximately 40% of patients with advanced melanoma who received nivolumab combined with ipilimumab in clinical trials discontinued treatment because of adverse events (AEs). We conducted a retrospective analysis to assess the efficacy and safety of nivolumab plus ipilimumab in patients who discontinued treatment because of AEs. Methods Data were pooled from phase II and III trials of patients who received nivolumab 1 mg/kg plus ipilimumab 3 mg/kg, every 3 weeks for four doses, followed by nivolumab monotherapy 3 mg/kg every 2 weeks (N = 409). Efficacy was assessed in all randomly assigned patients who discontinued because of AEs during the induction phase (n = 96) and in those who did not discontinue because of AEs (n = 233). Safety was assessed in treated patients who discontinued because of AEs (n = 176) at any time and in those who did not discontinue because of AEs (n = 231). Results At a minimum follow-up of 18 months, median progression-free survival was 8.4 months for patients who discontinued treatment because of AEs during the induction phase and 10.8 months for patients who did not discontinue because of AEs ( P = .97). Median overall survival had not been reached in either group ( P = .23). The objective response rate was 58.3% for patients who discontinued because of AEs during the induction phase and 50.2% for patients who did not discontinue. The vast majority of grade 3 or 4 AEs occurred during the induction phase, with most resolving after appropriate management. Conclusion Efficacy outcomes seemed similar between patients who discontinued nivolumab plus ipilimumab treatment because of AEs during the induction phase and those who did not discontinue because of AEs. Therefore, even after discontinuation, many patients may continue to derive benefit from combination therapy.Entities:
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Year: 2017 PMID: 28841387 PMCID: PMC5791828 DOI: 10.1200/JCO.2017.73.2289
Source DB: PubMed Journal: J Clin Oncol ISSN: 0732-183X Impact factor: 44.544