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

被引:28
作者
Algazi, A. P. [1 ]
Weber, J. S. [2 ]
Andrews, S. C. [2 ]
Urbas, P. [2 ]
Munster, P. N. [1 ]
DeConti, R. C. [2 ]
Hwang, J. [1 ]
Sondak, V. K. [2 ]
Messina, J. L. [2 ]
McCalmont, T. [1 ]
Daud, A. I. [1 ]
机构
[1] Univ Calif San Francisco, San Francisco, CA 94143 USA
[2] Univ S Florida, H Lee Moffitt Canc Ctr, Tampa, FL 33682 USA
关键词
melanoma; dasatinib; dacarbazine; Src; biomarkers; RECOMBINANT INTERLEUKIN-2 THERAPY; KINASE INHIBITOR; MOLECULAR MARKERS; PROSTATE-CANCER; KIT EXPRESSION; III TRIAL; CELLS; MUTATION; ACTIVATION; INVASION;
D O I
10.1038/bjc.2011.514
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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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页码:85 / 91
页数:7
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