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Minimal single-agent activity of maytansine in refractory breast cancer: a Southwest Oncology Group study.

Abstract
Maytansine is an experimental antitumor agent that has shown minimal efficacy against breast cancer with minimal myelosuppression in phase I trials. Forty-one patients with advanced drug-resistant breast cancer were treated with a 5-day intermittent iv infusion of maytansine repeated every 21 days. All patients had been heavily pretreated with cyclophosphamide, methotrexate, 5-fluorouracil, or doxorubicin, and 12 had received vinblastine, mitomycin C, or investigational drugs. All patients had measurable disease and an expected survival of 6 weeks. The average performance status was 2.5. Twelve patients did not complete one full cycle of therapy, leaving 29 evaluable for response. One patient had a partial regression of pulmonary disease, seven had transient responses of less than 50% reduction in tumor or stable disease, and 21 had progressive disease. Toxic effects (vomiting, diarrhea, ileus, lethargy, and altered mentation) were considerable. Since maytansine is a relatively nonmyelotoxic metaphase inhibitor, we feel that even minimal efficacy in heavily pretreated patients justifies further evaluation of the agent in combination therapy.
AuthorsJ A Neidhart, L R Laufman, C Vaughn, J D McCracken
JournalCancer treatment reports (Cancer Treat Rep) 1980 Apr-May Vol. 64 Issue 4-5 Pg. 675-7 ISSN: 0361-5960 [Print] United States
PMID7427953 (Publication Type: Journal Article, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Oxazines
  • Maytansine
Topics
  • Breast Neoplasms (drug therapy, mortality)
  • Drug Administration Schedule
  • Drug Evaluation
  • Drug Resistance
  • Female
  • Humans
  • Maytansine (administration & dosage, therapeutic use)
  • Middle Aged
  • Oxazines (therapeutic use)

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