Phase II multicenter study of epirubicin for hormone-resistant prostatic cancer with measurable soft tissue disease

Am J Clin Oncol. 1993 Apr;16(2):156-8. doi: 10.1097/00000421-199304000-00016.

Abstract

Twenty-six patients with prostatic cancer were treated with courses of epirubicin at 3-week intervals, starting at an initial intravenous dose of 75 mg/m2. All patients had progressive disease after orchiectomy and/or antiandrogen therapy and had measurable soft tissue lesions. There were three partial responders (response rate: 12%; 95% confidence limits: 4-29%). Major toxicity was myelosuppression, and there were two drug-related deaths. Epirubicin in this dose and schedule cannot be recommended for treatment of prostatic cancer.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase II
  • Multicenter Study

MeSH terms

  • Aged
  • Epirubicin / therapeutic use*
  • Humans
  • Male
  • Middle Aged
  • Prostatic Neoplasms / drug therapy*
  • Soft Tissue Neoplasms / drug therapy
  • Soft Tissue Neoplasms / secondary*
  • Survival Analysis

Substances

  • Epirubicin