Pretreatment with chlormadinone acetate eliminates testosterone surge induced by a luteinizing-hormone-releasing hormone analogue and the risk of disease flare in patients with metastatic carcinoma of the prostate

Eur Urol. 1995;27(3):187-91. doi: 10.1159/000475158.

Abstract

We investigated the efficacy of 2-week and 4-week pretreatments with 100 mg/day chlormadinone acetate (CMA) to prevent the flare reaction induced by luteinizing-hormone-releasing hormone (LHRH) in patients with metastatic carcinoma of the prostate. CMA lead-in therapy suppressed bone pain and serum levels of luteinizing hormone, testosterone and prostate-specific antigen levels. CMA therapy also suppressed the transient increases in these levels associated with the initiation of therapy. The 4-week regimen appeared to be more effective than the 2-week regimen.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Administration, Oral
  • Aged
  • Aged, 80 and over
  • Carcinoma / blood*
  • Carcinoma / prevention & control
  • Chlormadinone Acetate / therapeutic use*
  • Disease Progression
  • Gonadotropin-Releasing Hormone / adverse effects*
  • Humans
  • Injections, Subcutaneous
  • Luteinizing Hormone / blood*
  • Luteinizing Hormone / drug effects
  • Male
  • Middle Aged
  • Premedication
  • Prostate-Specific Antigen / blood*
  • Prostate-Specific Antigen / drug effects
  • Prostatic Neoplasms / blood*
  • Prostatic Neoplasms / prevention & control
  • Testosterone / blood*

Substances

  • Chlormadinone Acetate
  • Gonadotropin-Releasing Hormone
  • Testosterone
  • Luteinizing Hormone
  • Prostate-Specific Antigen