Cyclophosphamide, cisplatin, and leuprolide acetate in patients with debulked stage III or IV ovarian carcinoma

Gynecol Oncol. 1994 Aug;54(2):196-200. doi: 10.1006/gyno.1994.1192.

Abstract

A phase II study of cyclophosphamide, cisplatin, and leuprolide acetate after debulking of stage III or IV ovarian carcinoma was conducted in 33 patients through a cooperative group study involving 11 institutions. The intent was to determine whether the addition of a gonadotropin-releasing hormone analogue would alter the response rates and toxicity profile of cyclophosphamide and cisplatin in patients with advanced ovarian cancer. Twenty-nine patients completed all 6 planned cycles. Of the 19 patients who had second-look laparotomy, 12 had persistent disease and 7 were negative for disease. The use of a gonadotropin-releasing hormone with combined chemotherapy did not alter the toxicity profile or the effectiveness of chemotherapy when comparisons were made with historical controls.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase II
  • Multicenter Study
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use
  • Cisplatin / therapeutic use*
  • Cyclophosphamide / therapeutic use*
  • Drug Therapy, Combination
  • Female
  • Follicle Stimulating Hormone / blood
  • Humans
  • Laparotomy
  • Leuprolide / therapeutic use*
  • Middle Aged
  • Neoplasm Staging
  • Ovarian Neoplasms / blood
  • Ovarian Neoplasms / drug therapy*
  • Ovarian Neoplasms / pathology

Substances

  • Cyclophosphamide
  • Follicle Stimulating Hormone
  • Leuprolide
  • Cisplatin