Phase II trial of bisantrene in non-small cell lung cancer

Invest New Drugs. 1985;3(4):393-5. doi: 10.1007/BF00170764.

Abstract

Eighteen evaluable patients with non-small cell lung cancer (NSCLC) were treated with bisantrene at a dose of 200 mg/m2 once a week for 3 consecutive weeks. Courses of treatment were repeated every 4 weeks. This dose schedule caused leukopenia (less than 3,500 cells/microl) in all patients. There were no objective responses in 18 patients. Bisantrene in this myelosuppressive dose schedule did not have significant activity in patients with NSCLC.

Publication types

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

MeSH terms

  • Aged
  • Anthracenes / adverse effects
  • Anthracenes / therapeutic use
  • Antibiotics, Antineoplastic / therapeutic use*
  • Drug Evaluation
  • Female
  • Humans
  • Lung Neoplasms / drug therapy*
  • Male
  • Middle Aged

Substances

  • Anthracenes
  • Antibiotics, Antineoplastic
  • bisantrene