Long-term follow-up confirms a survival advantage of the paclitaxel-cisplatin regimen over the cyclophosphamide-cisplatin combination in advanced ovarian cancer

Int J Gynecol Cancer. 2003 Nov-Dec:13 Suppl 2:144-8. doi: 10.1111/j.1525-1438.2003.13357.x.

Abstract

Two independent and consecutive randomized clinical trials, conducted by the American Gynecological Oncology Group and by an European-Canadian Intergroup, have shown superiority, in clinical response rate, progression-free survival, and overall survival, of a cisplatin-paclitaxel regimen over cisplatin-cyclophosphamide given as first-line chemotherapy for women with advanced epithelial ovarian cancer. The results of these studies, published with a median follow-up of about 3 years, have been updated with a 6.5-year follow-up: In each case, an 11% absolute gain in survival favoring the paclitaxel arm is shown; this advantage remains both statistically and clinically significant and supports a role for paclitaxel in frontline chemotherapy for advanced ovarian cancer.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial

MeSH terms

  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Canada
  • Cisplatin / administration & dosage
  • Cyclophosphamide / administration & dosage
  • Europe
  • Female
  • Follow-Up Studies
  • Humans
  • Longitudinal Studies
  • Neoplasm Staging
  • Ovarian Neoplasms / drug therapy*
  • Ovarian Neoplasms / mortality*
  • Ovarian Neoplasms / pathology
  • Paclitaxel / administration & dosage
  • Randomized Controlled Trials as Topic
  • Survival Analysis

Substances

  • Cyclophosphamide
  • Paclitaxel
  • Cisplatin