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

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.
AuthorsG Dörner, D Schnorr, F Stahl, W Rohde
JournalExperimental and clinical endocrinology (Exp Clin Endocrinol) Vol. 86 Issue 2 Pg. 190-6 (Dec 1985) ISSN: 0232-7384 [Print] Germany
PMID3912197 (Publication Type: Journal Article)
Chemical References
  • Delayed-Action Preparations
  • ethinyl estradiol sulfonate
  • Gonadotropin-Releasing Hormone
  • Testosterone
  • Ethinyl Estradiol
Topics
  • Aged
  • Delayed-Action Preparations
  • Ethinyl Estradiol (adverse effects, analogs & derivatives, therapeutic use)
  • Gonadotropin-Releasing Hormone (therapeutic use)
  • Humans
  • Male
  • Middle Aged
  • Orchiectomy
  • Prostatic Neoplasms (drug therapy)
  • Testosterone (blood)

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