Clinical and clinical pharmacologic studies of aziridinylbenzoquinone

Cancer Treat Rep. 1982 Jun;66(6):1321-5.

Abstract

Thirty patients were entered in a phase I trial of aziridinylbenzoquinone (AZQ). These patients were treated with a single iv dose of AZQ daily for 5 days at doses ranging from 0.5 mg/m2 to 10.0 mg/m2. The dose-limiting and only significant toxic effects were leukopenia and thrombocytopenia, which appeared with relative consistency at iv dosages of 4.0--4.5 mg/m2/day x 5 in patients with extensive prior treatment and 7.0 mg/m2/day x 5 in patients with little prior treatment. One patient with colon cancer achieved a partial response of 4+ months. No other evidence of antitumor activity was observed. Pharmacologic studies revealed that the drug disappeared from the plasma in a biphasic manner (alpha-half-life = 1.5 minutes, beta-half-life = 18 minutes). With our method of analysis by high-performance liquid chromatography, no metabolites were found in the serum.

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Antineoplastic Agents / adverse effects
  • Antineoplastic Agents / metabolism
  • Antineoplastic Agents / therapeutic use*
  • Aziridines / adverse effects
  • Aziridines / metabolism
  • Aziridines / therapeutic use*
  • Azirines / therapeutic use*
  • Benzoquinones*
  • Cyclohexenes
  • Drug Evaluation
  • Female
  • Half-Life
  • Humans
  • Kinetics
  • Leukopenia / chemically induced
  • Male
  • Middle Aged
  • Neoplasms / drug therapy*
  • Thrombocytopenia / chemically induced

Substances

  • Antineoplastic Agents
  • Aziridines
  • Azirines
  • Benzoquinones
  • Cyclohexenes
  • 2,5-bis(1-aziridinyl)-3,6-bis(2-methoxyethoxy)-4-benzoquinone