Clinical experience with ipilimumab 10 mg/kg in patients with melanoma treated at Italian centres as part of a European expanded access programme

Background: patients with advanced melanoma are faced with a poor prognosis and,until recently,limited treatment options. ipilimumab,a novel immunotherapy that blocks cytotoxic t-lymphocyte-associated antigen-4,was the first agent to improve survival of patients with advanced melanoma in a randomised,controlled phase 3 trial. we used data from an expanded access programme (eap) at italian centres to evaluate the clinical activity and safety profile of ipilimumab 10 mg/kg in patients with advanced melanoma in a setting more similar to that of daily practice. methods. data were collected from patients enrolled in an ipilimumab eap across eight participating italian centres. as per the eap protocol,patients had life-threatening,unresectable stage iii/iv melanoma,had failed or did not tolerate previous treatments and had no other therapeutic option available. treatment comprised ipilimumab 10 mg/kg every 3 weeks for a total of four doses. if physicians believed patients would continue to derive benefit from ipilimumab treatment,maintenance therapy with ipilimumab 10 mg/kg was provided every 12 weeks. tumour responses were assessed every 12 weeks using modified world health organization criteria and safety continuously monitored. results: seventy-four pretreated patients with advanced melanoma were treated with ipilimumab 10 mg/kg. of these,9 (13.0%) had an objective response,comprising 3 patients with a complete response and 6 with a partial response. median overall survival was 7.0 months (95% confidence interval,5.3-8.7) and 16.6% of patients were alive after 3 years. forty-five patients (60.8%) reported treatment-related adverse events of any grade,which were most commonly low-grade pruritus,pain,fever and diarrhoea. grade 3 or 4 treatment-related aes were reported in 8 patients (10.8%). conclusions: the clinical activity and safety profile of ipilimumab 10 mg/kg in the eap was similar to that seen in previous clinical trials of ipilimumab in pretreated patient populations. © 2013 altomonte et al.; licensee biomed central ltd.