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Phase II study of mitolactol in chemotherapy-refractory metastatic breast cancer.

Abstract
Thirty-eight evaluable patients with metastatic breast cancer refractory to hormonal therapy and multiple chemotherapy regimens were treated with mitolactol at a dose of 130 mg/m2/day orally for 10 days every 6 weeks. Only one patient, with nodal and chest wall metastases, had a sustained complete regression; two patients had stable disease; and 35 patients had disease progression. The toxicity, which was primarily hematologic, was acceptable.
AuthorsR H Creech, R B Catalano, K M Dierks, M K Shah
JournalCancer treatment reports (Cancer Treat Rep) Vol. 68 Issue 12 Pg. 1499-501 (Dec 1984) ISSN: 0361-5960 [Print] United States
PMID6548936 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Antineoplastic Agents
  • Receptors, Estrogen
  • Cyclophosphamide
  • Mitolactol
  • Fluorouracil
  • Methotrexate
Topics
  • Adult
  • Aged
  • Antineoplastic Agents (therapeutic use)
  • Antineoplastic Combined Chemotherapy Protocols (therapeutic use)
  • Breast Neoplasms (drug therapy)
  • Cyclophosphamide (administration & dosage)
  • Drug Evaluation
  • Female
  • Fluorouracil (administration & dosage)
  • Humans
  • Methotrexate (administration & dosage)
  • Middle Aged
  • Mitolactol (therapeutic use, toxicity)
  • Neoplasm Metastasis
  • Receptors, Estrogen (analysis)

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