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

Abstract
Twenty-six patients with far-advanced, refractory breast cancer were treated iv with vindesine (DVA) at a dose of 3 mg/m2/week. In 21 evaluable patients there were six partial remissions. Four patients who did not respond after at least four doses of intermittent DVA received continuous-infusion DVA at a dose of 1.5 mg/m2/day X 2 every other week; none responded. Five of the six responders had had disease progression on other vinca alkaloids. Leukopenia and neuromuscular toxicity were dose-limiting.
AuthorsM A Cobleigh, S D Williams, L H Einhorn
JournalCancer treatment reports (Cancer Treat Rep) 1981 Jul-Aug Vol. 65 Issue 7-8 Pg. 659-63 ISSN: 0361-5960 [Print] United States
PMID7248983 (Publication Type: Journal Article)
Chemical References
  • Vinblastine
  • Vindesine
Topics
  • Breast Neoplasms (drug therapy)
  • Drug Administration Schedule
  • Drug Evaluation
  • Female
  • Humans
  • Leukopenia (chemically induced)
  • Neoplasm Metastasis
  • Neuromuscular Diseases (chemically induced)
  • Prognosis
  • Vinblastine (adverse effects, analogs & derivatives, therapeutic use)
  • Vindesine

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