A phase II study of fazarabine in patients with advanced ovarian cancer. A Gynecologic Oncology Group study

Am J Clin Oncol. 1995 Apr;18(2):156-7. doi: 10.1097/00000421-199504000-00012.

Abstract

Background: A total of 22 patients with recurrent ovarian cancer previously treated with cisplatin-containing chemotherapy were treated with Fazarabine.

Methods: The drug was administered at an initial dose of 30 mg/m2/day for 5 consecutive days. Cycles were repeated every 28 days. There were 19 evaluable patients.

Results: No complete or partial responders were observed in this study; 48% of patients were deemed to have stable disease. The major toxicity was hematologic, with four patients exhibiting grade 4 neutropenia.

Conclusions: Fazarabine shows no useful activity as a single agent when given at this dose and schedule in the management of previously treated patients with cancer of the ovary.

Publication types

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

MeSH terms

  • Adenocarcinoma / drug therapy
  • Antineoplastic Agents / adverse effects
  • Antineoplastic Agents / therapeutic use*
  • Azacitidine / adverse effects
  • Azacitidine / therapeutic use*
  • Female
  • Humans
  • Infusions, Intravenous
  • Neoplasm Recurrence, Local / drug therapy*
  • Ovarian Neoplasms / drug therapy*
  • Treatment Outcome

Substances

  • Antineoplastic Agents
  • fazarabine
  • Azacitidine