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Efficacy and safety of ipilimumab in patients with advanced melanoma and brain metastases
Authors:Paola Queirolo  Francesco Spagnolo  Paolo Antonio Ascierto  Ester Simeone  Paolo Marchetti  Alessandro Scoppola  Michele Del Vecchio  Lorenza Di Guardo  Michele Maio  Anna Maria Di Giacomo  Andrea Antonuzzo  Francesco Cognetti  Virginia Ferraresi  Laura Ridolfi  Massimo Guidoboni  Michele Guida  Jacopo Pigozzo  Vanna Chiarion Sileni
Affiliation:12. Medical Oncology, IRCCS Azienda Ospedaliera Universitaria San Martino – IST Istituto Nazionale per la Ricerca sul Cancro, Largo Rosanna Benzi, 10, 16132, Genova, Italy
1. Department of Plastic and Reconstructive Surgery – IRCCS San Martino – IST Istituto Nazionale per la Ricerca sul Cancro, Genova, Italy
2. Cancer Immunotherapy and Innovative Therapy Unit, National Cancer Institute IRCCS “Fondazione G. Pascale”, Naples, Italy
3. Medical Oncology, Dermopathic Institute of the Immaculate IDI-IRCCS, Rome, Italy
4. Medical Oncology, Sant’ Andrea Hospital, Sapienza University of Rome, Rome, Italy
5. Department of Medical Oncology, IRCCS Foundation National Cancer Institute, Milan, Italy
6. Department of Medical Oncology and Immunotherapy, Tuscan Tumor Institute (ITT), University Hospital of Siena, Siena, Italy
7. Department of Medical Oncology, University Hospital Pisa, “Gathered Hospitals of Santa Chiara”, Pisa, Italy
8. Department of Medical Oncology, Regina Elena National Cancer Institute, Rome, Italy
9. Department of Medical Oncology, Scientific Institute of Romagna for the Study and Treatment of Cancer (IRCCS-IRST), Meldola, Italy
10. “Giovanni Paolo II” Cancer Institute (IRCCS), Bari, Italy
11. Melanoma Cancer Unit, Veneto Institute of Oncology IOV-IRCCS, Padua, Italy
Abstract:
Patients with melanoma brain metastases have a poor prognosis and historically have been excluded from clinical trials. The Expanded Access Program (EAP) provided an opportunity to evaluate the feasibility of ipilimumab (3 mg/kg every 3 weeks for four doses) in patients with stage 3 (unresectable) or 4 melanoma and asymptomatic brain metastases, who had failed or did not tolerate previous treatments and had no other therapeutic option available. Tumor assessments were conducted at baseline and week 12 using immune-related response criteria and patients were monitored for adverse events (AEs). Of 855 patients participating in the EAP in Italy, 146 had asymptomatic brain metastases. With a median follow-up of 4 months, the global disease control rate was 27 %, including 4 patients with a complete response and 13 with a partial response. Median progression-free survival and overall survival were 2.8 and 4.3 months, respectively and approximately one-fifth of patients were alive 1 year after starting ipilimumab. In total, 29 % of patients reported a treatment-related AE of any grade, which were grade 3/4 in 6 % of patients. AEs were generally reversible with treatment as per protocol-specific guidelines. Ipilimumab shows durable benefits in some patients with advanced melanoma metastatic to the brain, with safety results consistent with those previously reported in clinical trials.
Keywords:
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