The Duke AFM Program. Intensive induction chemotherapy for metastatic breast cancer

Cancer. 1990 Aug 1;66(3):431-6. doi: 10.1002/1097-0142(19900801)66:3<431::aid-cncr2820660305>3.0.co;2-x.

Abstract

Forty-five patients have completed treatment with AFM, an intensive induction chemotherapy regimen composed of Adriamycin (doxorubicin, Adria Laboratories, Columbus, Ohio), 5-fluorouracil, and methotrexate with folinic acid rescue. This regimen was designed to produce rapid and extensive tumor shrinkage prior to high-dose alkylating agent chemotherapy with autologous marrow support. The overall response rate was 91%, and 38% of patients achieved complete clinical responses after a mean of 70 days on treatment. Hematologic and mucosal toxicity were extensive, but no toxic deaths were noted. AFM is a potent remission induction regimen for metastatic breast cancer, but its considerable toxicity suggests caution in its use for routine breast cancer treatment.

Publication types

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

MeSH terms

  • Adult
  • Antineoplastic Combined Chemotherapy Protocols / adverse effects
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / pathology
  • Doxorubicin / administration & dosage
  • Doxorubicin / adverse effects
  • Drug Administration Schedule
  • Drug Evaluation
  • Female
  • Fluorouracil / administration & dosage
  • Fluorouracil / adverse effects
  • Humans
  • Leukopenia / chemically induced
  • Methotrexate / administration & dosage
  • Methotrexate / adverse effects
  • Middle Aged
  • Mucous Membrane / drug effects
  • Remission Induction

Substances

  • Doxorubicin
  • Fluorouracil
  • Methotrexate

Supplementary concepts

  • AMF protocol