Phase II study of teniposide in adenocarcinoma of the lung

Cancer Chemother Pharmacol. 1991;27(6):487-9. doi: 10.1007/BF00685166.

Abstract

A total of 26 evaluable patients with previously untreated, non-resectable adenocarcinoma of the lung were given 80 mg/m2 i.v. teniposide daily for 5 days every 3 weeks. Three partial responses (11%) were obtained that lasted for 12, 11 and 32 weeks, respectively. Leucopenia was the dose-limiting side effect, with WBC counts of less than 2 x 10(9)/l being observed in 42% of patients, resulting in one septic death. At the dose and schedule used in the present study, teniposide showed only limited activity in adenocarcinoma of the lung.

MeSH terms

  • Adenocarcinoma / drug therapy*
  • Adult
  • Aged
  • Drug Administration Schedule
  • Drug Evaluation
  • Female
  • Humans
  • Leukopenia / chemically induced
  • Lung Neoplasms / drug therapy*
  • Male
  • Middle Aged
  • Remission Induction
  • Teniposide / administration & dosage
  • Teniposide / adverse effects
  • Teniposide / therapeutic use*
  • Thrombocytopenia / chemically induced

Substances

  • Teniposide