Etoposide in prostatic cancer: experimental studies and phase II trial in patients with bidimensionally measurable disease Academic Article Article uri icon


MeSH Major

  • Gastrointestinal Neoplasms
  • HIV Infections
  • Neuroendocrine Tumors
  • Pancreatic Neoplasms


  • Etoposide, a semisynthetic derivative of podophyllotoxin, was evaluated concurrently in vitro against a human derived hormone-resistant cell line, PC-3, and in vivo in bidimensionally measurable hormone-resistant human prostatic cancer. In vitro, a dose-response relationship was observed, with 74% inhibition at 10 micrograms/ml (1 h incubation) and greater than 99% inhibition at 90 micrograms/ml, both in the range of clinically achievable concentrations. In vivo, 1 PR (5%, 95% confidence limits 0-12%) of 18+ months was observed in 20 adequately treated patients. The results confirm the limited role of etoposide in hormone-refractory disease and the need for new model systems for evaluation of potential chemotherapeutic compounds in this disease.

publication date

  • September 1986



  • Academic Article


Digital Object Identifier (DOI)

  • 10.1007/BF00253058

PubMed ID

  • 3757155

Additional Document Info

start page

  • 24

end page

  • 6


  • 18


  • 1