Phase I trial of echinomycin (NSC 526417), a bifunctional intercalating agent, administered by 24-hour continuous infusion

Eur J Cancer Clin Oncol. 1989 May;25(5):797-803. doi: 10.1016/0277-5379(89)90123-5.

Abstract

Echinomycin was administered to 43 patients with advanced cancer in escalating doses ranging from 60 to 2128 mcg/m2. The dose-limiting toxicity of echinomycin administered as a 24-h continuous infusion every 28 days was nausea and vomiting beginning at the end of the 24 h infusion and lasting from 3 to 8 days. Other toxicities included sporadic thrombocytopenia and biochemical evidence of liver dysfunction characterized by elevations in SGOT. Peripheral vein phlebitis was noted in 100% of patients, and watery diarrhea of 24-48-h duration was noted in 7% of patients. The maximally tolerated dose of echinomycin was 2128 mcg/m2. The recommended dose for phase II trials utilizing the 24-h continuous infusion schedule is 1600 mcg/m2 repeated every 28 days with pretreatment antiemetics.

Publication types

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

MeSH terms

  • Adult
  • Aged
  • Drug Evaluation
  • Echinomycin / administration & dosage*
  • Echinomycin / toxicity
  • Female
  • Humans
  • Infusions, Intravenous
  • Liver Function Tests
  • Male
  • Middle Aged
  • Nausea / chemically induced
  • Neoplasms / drug therapy
  • Platelet Count / drug effects
  • Quinoxalines / administration & dosage*
  • Thrombocytopenia / chemically induced
  • Vomiting / chemically induced

Substances

  • Quinoxalines
  • Echinomycin