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ABSTRACT: Purpose
To determine safety and feasibility of adjuvant ipilimumab following resection of high-risk melanoma and to identify surrogate markers for benefit.Experimental design
In this phase II trial, 75 patients with resected stage IIIc/IV melanoma received the CTLA-4 antibody ipilimumab every 6 to 8 weeks for 1 year. Eligible patients received further maintenance treatments. The first 25 patients received 3 mg/kg of ipilimumab, and an additional 50 patients received 10 mg/kg. HLA-A*0201+ patients received multipeptide immunizations in combination with ipilimumab. Leukapheresis was performed prior to and 6 months after initiation of treatment.Results
Median overall and relapse-free survivals were not reached after a median follow-up of 29.5 months. Significant immune
SUBMITTER: Sarnaik AA
PROVIDER: S-EPMC3041838 | biostudies-literature | 2011 Feb
REPOSITORIES: biostudies-literature