[Chemotherapy of hormone-resistent cancer of the prostate]

Urologiia. 2005 Jul-Aug:(4):20-3.
[Article in Russian]

Abstract

A total of 59 patients with hormone-resistent prostatic cancer (HDPC) treated in 1999-2004 entered the trial. Three schemes of first-line chemotherapy were examined for clinical efficacy and toxicity in the above patients. Anticancer combined treatment vinorelbin + cycloplatam was given to 23 patients, mitoxantron + prednisolone--to 23 patients, mitoxantron+cysplatin+prednisolone--to 13 patients. The latter scheme was most effect and toxic. Partial regression of metastases and a 50% decrease in the initial PCA level were seen in 23% cases. Vinorelbin+cycloplatam was less effective and toxic: partial regression of metastases--13%, PSA regression-- 17.4%. The least efficacy and toxicity were observed in the treatment with mitoxantron+prednisolone --.7%. Thus, the above first-line HDPC therapy was most effective but has the highest toxicity in using the scheme mitoxantron+cysplatin+prednisolone.

Publication types

  • Clinical Trial
  • Comparative Study
  • Controlled Clinical Trial

MeSH terms

  • Aged
  • Antineoplastic Agents, Hormonal / therapeutic use
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Bone Neoplasms / prevention & control
  • Bone Neoplasms / secondary
  • Cisplatin / administration & dosage
  • Drug Resistance, Neoplasm
  • Humans
  • Male
  • Middle Aged
  • Mitoxantrone / administration & dosage
  • Organoplatinum Compounds / administration & dosage
  • Prednisolone / administration & dosage
  • Prostatic Neoplasms / drug therapy*
  • Prostatic Neoplasms / pathology
  • Treatment Outcome
  • Vinblastine / administration & dosage
  • Vinblastine / analogs & derivatives
  • Vinorelbine

Substances

  • Antineoplastic Agents, Hormonal
  • Organoplatinum Compounds
  • cycloplatam
  • Vinblastine
  • Prednisolone
  • Mitoxantrone
  • Cisplatin
  • Vinorelbine