4.7 Article

Phase I clinical trial of the Src inhibitor dasatinib with dacarbazine in metastatic melanoma

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BRITISH JOURNAL OF CANCER
卷 106, 期 1, 页码 85-91

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DOI: 10.1038/bjc.2011.514

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melanoma; dasatinib; dacarbazine; Src; biomarkers

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  1. Bristol-MyersSquibb

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BACKGROUND: Src inhibitors sensitise melanoma cells to chemotherapy in preclinical models. The combination of dasatinib and dacarbazine was tested in a phase I trial in melanoma. METHODS: Patients had ECOG performance status 0-2 and normal organ function. Dacarbazine was administered on day 1 and dasatinib on day 2 through 19 of each 21-day cycle. Both were escalated from 50 mg b.i.d. of dasatinib and 800 mgm(-2) of dacarbazine. Available pre-treatment biopsies were sequenced for BRAF, NRAS, and C-Kit mutations. RESULTS: Dose-limiting toxicity was reached at dasatinib 70 mg b.i.d./dacarbazine 1000 mgm(-2), and was predominantly haematological. In 29 patients receiving dasatinib 70 mg b.i.d., the objective response rate (ORR) was 13.8%, the clinical benefit rate (ORR+SD) was 72.4%, the 6-month progression-free survival (PFS) was 20.7%, and the 12-month overall survival (OS) was 34.5%. Two out of three patients who were wild type for BRAF, NRAS, and c-KIT mutations had confirmed partial responses, and one had a minor response. CONCLUSION: The recommended phase II dose is dasatinib70 mg b.i.d with dacarbazine 800 mgm(-2). PFS and OS data for dasatinib at 70 mg b.i.d. with dacarbazine compared favourably with historical controls. Preliminary data support evaluating tumour mutation status further as a biomarker of response. British Journal of Cancer (2012) 106, 85-91. doi:10.1038/bjc.2011.514 www.bjcancer.com Published online 29 November 2011 (C) 2012 Cancer Research UK

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