Phase IV trial of daily oral etoposide in the treatment of advanced soft-tissue sarcoma

Cancer Chemother Pharmacol. 1994;34(1):79-80. doi: 10.1007/BF00686117.

Abstract

Intravenous-bolus etoposide has modest activity in sarcomas when given daily for 3-5 days. Low frequent doses theoretically inhibit topoisomerase II activity over a longer duration and have been reported to have increased activity in small-cell lung cancer. A phase I trial of oral etoposide resulted in partial responses in two patients with soft-tissue sarcomas. To estimate more accurately the response rate for daily oral etoposide in sarcomas, we treated 25 patients with 50 mg/m2 per day by mouth for 21 days every 4 weeks. Treatment-related toxicity included > or = grade 2 neutropenia in 6 of the 25 patients and thrombocytopenia in 3. One brief partial response was observed (4%; 95% confidence interval for true response rate, 0-11%). Disease stabilized in five patients for periods ranging from 3 to 18 months. At this dose and on this schedule, daily oral etoposide appears to have little activity against soft-tissue sarcomas.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase IV

MeSH terms

  • Administration, Oral
  • Adult
  • Aged
  • Drug Administration Schedule
  • Etoposide / administration & dosage
  • Etoposide / therapeutic use*
  • Female
  • Humans
  • Male
  • Middle Aged
  • Sarcoma / drug therapy*
  • Sarcoma / secondary

Substances

  • Etoposide