Successful treatment of prostatic cancer with the orally active depot estrogen ethinylestradiol sulfonate (Turisteron)

Exp Clin Endocrinol. 1985 Dec;86(2):190-6. doi: 10.1055/s-0029-1210486.

Abstract

Ethinylestradiol sulfonate (Turisteron) is an orally highly active depot-estrogen with relatively low side effects. In men with prostatic cancer, weekly administration of 2 mg Turisteron resulted in a striking decrease of the biologically active free testosterone level to less than 2% of the basal level; i.e., even significantly lower than after orchidectomy. Turisteron was able to normalize the 5 year survival rate in men with advanced non-metastatic cancer (T3NxM0) and to increase the survival rate significantly in men with metastatic cancer (T3-4, Nx, M1). Hence, due to our experience, Turisteron treatment is a very effective, non-expensive and well tolerated therapy for prostatic cancer.

MeSH terms

  • Aged
  • Delayed-Action Preparations
  • Ethinyl Estradiol / adverse effects
  • Ethinyl Estradiol / analogs & derivatives*
  • Ethinyl Estradiol / therapeutic use
  • Gonadotropin-Releasing Hormone / therapeutic use
  • Humans
  • Male
  • Middle Aged
  • Orchiectomy
  • Prostatic Neoplasms / drug therapy*
  • Testosterone / blood

Substances

  • Delayed-Action Preparations
  • ethinyl estradiol sulfonate
  • Gonadotropin-Releasing Hormone
  • Testosterone
  • Ethinyl Estradiol