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Phase II study of vindesine in patients with advanced breast cancer.

作者信息

Walker B K, Raich P C, Fontana J, Subramanian V P, Rogers J S, Knost J A, Denning B

出版信息

Cancer Treat Rep. 1982 Sep;66(9):1729-32.

PMID:6288237
Abstract

Vindesine, a new vinca alkaloid, was administered to 20 patients with advanced refractory breast cancer in a phase II trial. The drug was given at a dose of 3 mg/m2 by iv bolus each week for 6 consecutive weeks, and responding patients were maintained on a dose of 4 mg/m2 every 2 weeks. Nineteen patients were evaluable for disease response; partial remissions were obtained in five patients, for a response rate of 26%. Leukopenia was the major dose-limiting toxic reaction, but most patients were able to tolerate this schedule without difficulty. Neurotoxicity was mild and did not require dose reduction.

摘要

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