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Insights

Drostanolone propionate (Masteril) showed promise as a safe and useful agent across menopausal stages. While effective, it was less potent than oestrogens in postmenopausal patients but demonstrated good results in premenopausal and perimenopausal groups.

Area of Science:

  • Endocrinology
  • Oncology
  • Pharmacology

Background:

  • Hormone replacement therapy is crucial for managing menopausal symptoms.
  • Anabolic-androgenic steroids (AAS) have been explored for therapeutic applications.
  • Drostanolone propionate (Masteril) is an AAS with potential clinical uses.

Purpose of the Study:

  • To evaluate the efficacy and safety of drostanolone propionate (Masteril) compared to established treatments.
  • To assess Masteril's effectiveness across different menopausal stages: premenopausal, perimenopausal, and postmenopausal.

Main Methods:

  • A clinical trial conducted from 1968 to 1972.
  • Masteril was compared against oophorectomy (premenopausal), nandrolone phenylpropionate (perimenopausal), and ethinyl oestradiol (postmenopausal).
  • Response rates and side-effects were recorded for each treatment group.

Main Results:

  • In premenopausal patients, 44% responded to Masteril versus 22% to oophorectomy.
  • In perimenopausal patients, 34.5% responded to Masteril versus 39% to nandrolone phenylpropionate.
  • In postmenopausal patients, 38.5% responded to Masteril versus 57% to ethinyl oestradiol.
  • Masteril exhibited generally mild and rarely contraindicating side-effects.

Conclusions:

  • Drostanolone propionate (Masteril) is a useful and safe agent for patients across all menopausal stages.
  • Masteril demonstrated efficacy in premenopausal and perimenopausal groups.
  • While effective, Masteril appeared less potent than oestrogens in postmenopausal patients.

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