New, expanded, and modified use of approved antineoplastic agents in ovarian cancer

Maurie Markman1

  • 1Department of Gynecologic Medical Oncology, University of Texas M.D. Anderson Cancer Center (Mail Box 121), 1515 Holcombe Boulevard, Houston, Texas 77030, USA. mmarkman@mdanderson.org

The Oncologist
|February 14, 2007
PubMed

Insights

Clinical research in ovarian cancer has improved systemic therapy effectiveness and reduced toxicity using FDA-approved drugs. Future studies with novel agents will further enhance treatment options for ovarian cancer patients.

Area of Science:

  • Oncology
  • Pharmacology

Background:

  • Ovarian cancer treatment has advanced through clinical research.
  • Systemic therapy effectiveness and toxicity have been improved.

Purpose of the Study:

  • To review the development of improved systemic therapy approaches for ovarian cancer.
  • To highlight the use of FDA-approved antineoplastic agents in ovarian cancer treatment.

Main Methods:

  • Review of prospective clinical trials and retrospective analyses.
  • Examination of U.S. Food and Drug Administration (FDA)-approved antineoplastic agents.

Main Results:

  • Established FDA-approved drugs (cisplatin, paclitaxel, topotecan, liposomal doxorubicin) have been utilized.
  • New strategies involve drugs approved for other cancers (gemcitabine, docetaxel, etoposide, irinotecan, vinorelbine, bevacizumab).

Conclusions:

  • Clinical research has led to more effective and less toxic ovarian cancer systemic therapies.
  • Ongoing studies with novel agents are expected to expand therapeutic options.

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