Phase II study with sequential L-asparaginase and methotrexate in advanced refractory breast cancer

Cancer Treat Rep. 1979 Jan;63(1):77-83.

Abstract

The combination of sequential L-asparaginase and methotrexate (MTX) was evaluated in 33 patients with advanced refractory breast cancer. There were nine partial responses and one complete response, giving an overall response rate of 30% and a median duration of response of 8 months. Five of 17 patients (28%) who had received prior MTX at doses of less than 50 mg/m2 responded. Toxicity was acceptable. Moderate-to-severe stomatitis occurred in most patients and was the dose-limiting factor. Myelosuppression was minimal until the dose of MTX was escalated to greater than or equal to 180 mg/m2. The maximum tolerated dose of MTX was 280 mg/m2 and the median toxic dose was 220 mg/m2. These data indicate a selective "rescue" from MTX damage to normal target tissue by L-asparaginase. The antitumor effect observed even in patients who had been previously exposed to conventional doses of MTX suggests a possible improved therapeutic index of MTX given sequentially with L-asparaginase in this combination.

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Asparaginase / administration & dosage
  • Asparaginase / adverse effects
  • Asparaginase / therapeutic use*
  • Blood Cell Count
  • Breast Neoplasms / drug therapy*
  • Clinical Trials as Topic
  • Drug Evaluation
  • Drug Therapy, Combination
  • Female
  • Humans
  • Methotrexate / administration & dosage
  • Methotrexate / adverse effects
  • Methotrexate / therapeutic use*
  • Middle Aged
  • Neoplasm Metastasis
  • Time Factors

Substances

  • Asparaginase
  • Methotrexate