Phase II study of ispinesib in recurrent or metastatic squamous cell carcinoma of the head and neck

被引:72
|
作者
Tang, Patricia A. [5 ]
Siu, Lillian L. [5 ]
Chen, Eric X. [5 ]
Hotte, Sebastien J. [5 ]
Chia, Stephen [5 ]
Schwarz, James K. [5 ]
Pond, Gregory R. [5 ]
Johnson, Caitlin [5 ]
Colevas, A. Dimitrios [4 ]
Synold, Timothy W. [3 ]
Vasist, Lakshmi S. [2 ]
Winquist, Eric [1 ,5 ]
机构
[1] London Hlth Sci Ctr, London, ON N6A 4L6, Canada
[2] GlaxoSmithKline, Dept Clin Pharmacokinet Modeling & Simulat, Res Triangle Pk, NC USA
[3] City Hope Comprehens Canc Ctr, Dept Clin & Mol Pharmacol, Div Med Oncol, Duarte, CA USA
[4] Stanford Univ, Med Ctr, Dept Med, Div Oncol, Stanford, CA 94305 USA
[5] Princess Margaret Phase II Consortium, Toronto, ON, Canada
关键词
head and neck neoplasms; hsEg5; ispinesib; kinesin spindle protein; phase II; squamous;
D O I
10.1007/s10637-007-9098-8
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Ispinesib (SB-715992) inhibits the mitotic kinesin spindle protein (KSP), a novel target for anticancer therapy. A phase II study was conducted to examine the efficacy of ispinesib in recurrent or metastatic head and neck squamous cell carcinoma (RMHNSC). Patients with up to one prior line of chemotherapy for RMHNSC were treated with ispinesib 18 mg/m(2) IV over 1 hour every 21 days. Twenty-one patients were enrolled onto this study with a target stage I sample size of 19. Of 20 evaluable patients, no objective responses were seen and stable disease > 2 cycles was observed in five patients (25%). The median time to progression was 1.4 (95% CI 1.3-2.3) months, median survival was 3.5 (95% CI 2.8-7.8) months, and 1 year overall survival was 20% (95% CI 8.3-48.1%). The most frequent attributable grades III-V adverse events were neutropenia (60% of patients) and leukopenia (55%). The pharmacokinetic profile was consistent with results from phase I studies. Archival tissues (n = 14) demonstrated low to moderate KSP expression by immunohistochemistry. In addition, no pharmacodynamic changes were observed in peripheral blood mononuclear cells. We detected no antitumor activity of ispinesib in RMHNSC on this dosing schedule.
引用
收藏
页码:257 / 264
页数:8
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