Adriamycin (doxorubicin), vinblastine, and mitomycin C combination chemotherapy in refractory breast carcinoma

Cancer. 1984 Oct 1;54(7):1252-5. doi: 10.1002/1097-0142(19841001)54:7<1252::aid-cncr2820540703>3.0.co;2-6.

Abstract

Twenty-seven evaluable patients with refractory, metastatic breast carcinoma were treated with Adriamycin (doxorubicin) 30 mg/m2 and vinblastine 6 mg/m2 intravenously on days 1 and 28 every 8 weeks, and mitomycin C 10 mg/m2 intravenously on day 1 every 8 weeks (AVM). There were three complete and six partial responses for a total response rate of 33%. In addition, 2 patients had minimal responses, and 10 patients achieved disease stabilization. Median time to disease progression for responders was 116 days (range, 49-812+ days). Drug toxicity was tolerable: 12 patients (44%) experienced significant bone marrow suppression. There were no drug-related deaths. Although AVM appears to be an active drug combination in heavily pretreated patients with metastatic breast carcinoma, the contribution of vinblastine and mitomycin C to single agent Adriamycin in previously treated patients is not clear from this study.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Breast Neoplasms / drug therapy*
  • Doxorubicin / administration & dosage
  • Doxorubicin / adverse effects
  • Drug Resistance
  • Female
  • Hematologic Diseases / chemically induced
  • Humans
  • Middle Aged
  • Mitomycin
  • Mitomycins / administration & dosage
  • Mitomycins / adverse effects
  • Vincristine / administration & dosage
  • Vincristine / adverse effects

Substances

  • Mitomycins
  • Mitomycin
  • Vincristine
  • Doxorubicin

Supplementary concepts

  • VAM protocol