Treatment of advanced prostatic cancer with LHRH analogue ICI 118630: clinical response and hormonal mechanisms

S R Ahmed, S M Shalet, P J Brooman, A Howell, N J Blacklock, D Rickards

Research output: Contribution to journalArticlepeer-review

Abstract

9 of 12 patients with advanced metastatic carcinoma of the prostate treated with luteinising-hormone-releasing-hormone (LHRH) analogue ICI 118630 for a mean period of 6 months showed objective evidence of response to treatment. Of 8 patients with bone pain, 7 obtained relief. After 6 weeks of treatment testosterone concentrations were reduced to castrate levels (range less than 2 to 5.5 nmol/l) from a pretreatment mean value of 15.7 nmol/l (range 10.3-24 nmol/l). Basal gonadotropin levels and gonadotropin responses to acute LHRH stimulation were suppressed within 2 weeks of treatment. However, the testosterone response to stimulation with human chorionic gonadotropin was unimpaired 4 weeks after the start of treatment. Therefore suppression of the basal testosterone concentration by ICI 118630 was due to inhibition of pituitary luteinising-hormone secretion rather than direct inhibition of testicular Leydig-cell function. ICI 118630 offers an alternative treatment to orchidectomy and oestrogen therapy.

Original languageEnglish
Pages (from-to)415-419
Number of pages5
JournalLancet (London, England)
Volume322
Issue number8347
Publication statusPublished - 20 Aug 1983

Keywords

  • Acid Phosphatase
  • Aged
  • Bone Neoplasms
  • Chorionic Gonadotropin
  • Depression, Chemical
  • Gonadotropin-Releasing Hormone
  • Goserelin
  • Humans
  • Lymphatic Metastasis
  • Male
  • Middle Aged
  • Pain
  • Pelvis
  • Prostatic Neoplasms
  • Radiography
  • Testosterone
  • Journal Article
  • Research Support, Non-U.S. Gov't

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