Oral etoposide in the treatment of hormone-refractory prostate cancer

Cancer. 1994 Jul 1;74(1):100-3. doi: 10.1002/1097-0142(19940701)74:1<100::aid-cncr2820740118>3.0.co;2-k.

Abstract

Background: Hormone-refractory prostate cancer generally remains a chemotherapy-resistant tumor and therefore warrants the continued evaluation of promising agents.

Methods: Twenty-two eligible patients with hormone-refractory prostate cancer were treated with oral etoposide at a dosage of 50 mg/m2/day for 21 days in a 28-day cycle. Response was evaluated using standard solid tumor response criteria.

Results: There were two partial responses of 6 and 14 months' duration, respectively. Two patients had disease stabilization, one for 6 months and one for 12 months. Median survival was 31 weeks, with an overall 1-year survival of 30%. Reversible alopecia and myelosuppression were the primary toxicities noted.

Conclusions: Single-agent oral etoposide has minimal activity in patients with hormone-refractory prostate cancer.

MeSH terms

  • Adenocarcinoma / drug therapy*
  • Adenocarcinoma / mortality
  • Administration, Oral
  • Aged
  • Aged, 80 and over
  • Androgen Antagonists / therapeutic use
  • Drug Administration Schedule
  • Drug Resistance
  • Etoposide / administration & dosage*
  • Etoposide / therapeutic use
  • Humans
  • Male
  • Middle Aged
  • Orchiectomy
  • Prostatic Neoplasms / drug therapy*
  • Prostatic Neoplasms / mortality
  • Remission Induction
  • Survival Rate

Substances

  • Androgen Antagonists
  • Etoposide