Population-based pharmacoeconomic model for adopting capecitabine/docetaxel combination treatment for anthracycline-pretreated metastatic breast cancer

Oncologist. 2003;8(3):232-40. doi: 10.1634/theoncologist.8-3-232.

Abstract

Purpose: To model the cost-effectiveness of adopting capecitabine/docetaxel combination therapy in place of single-agent taxane therapy for women in the province of Ontario, Canada, receiving treatment for anthracycline-pretreated metastatic breast cancer.

Methods: Clinical effectiveness and economic data were combined in a population model, from the perspective of a universal health care system. Estimates of clinical effectiveness and medical resource utilization were derived prospectively during a phase III randomized controlled trial comparing single-agent docetaxel with capecitabine/docetaxel combination therapy. Population data were obtained from the Cancer Care Ontario Registry and provincial prescription claims data.

Results: During 1999-2000, 542 patients were eligible for taxane monotherapy. As capecitabine/docetaxel treatment confers a median 3-month survival benefit compared with docetaxel monotherapy, the projected survival gain in these patients was 136 life-years. The results of the cost-effectiveness analysis demonstrate that the survival benefit provided by the addition of capecitabine to single-agent docetaxel is afforded at a small incremental cost of Canadian $3,691 per life-year gained. Hospitalization costs for treatment of adverse events were less for patients receiving capecitabine/docetaxel combination therapy than for those receiving docetaxel monotherapy. The results were robust for adjustments in treatment costs and adverse effects costs.

Conclusion: Due to its 3-month survival gain and small incremental treatment cost, capecitabine/docetaxel is judged to be a highly cost-effective treatment in anthracycline-pretreated advanced breast cancer. From the perspective of the Ontario health care system, the addition of capecitabine to docetaxel in this patient population is a clinically appropriate and economically acceptable treatment strategy.

Publication types

  • Clinical Trial
  • Clinical Trial, Phase III
  • Comparative Study
  • Randomized Controlled Trial

MeSH terms

  • Antibiotics, Antineoplastic / economics*
  • Antibiotics, Antineoplastic / therapeutic use*
  • Antibodies, Monoclonal / administration & dosage
  • Antibodies, Monoclonal / economics
  • Antibodies, Monoclonal, Humanized
  • Antimetabolites, Antineoplastic / administration & dosage*
  • Antimetabolites, Antineoplastic / economics*
  • Antineoplastic Agents, Phytogenic / administration & dosage*
  • Antineoplastic Agents, Phytogenic / economics*
  • Antineoplastic Combined Chemotherapy Protocols / economics*
  • Antineoplastic Combined Chemotherapy Protocols / therapeutic use*
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / economics*
  • Breast Neoplasms / mortality
  • Bridged-Ring Compounds / administration & dosage
  • Bridged-Ring Compounds / economics
  • Budgets
  • Capecitabine
  • Cost-Benefit Analysis / economics
  • Deoxycytidine / administration & dosage*
  • Deoxycytidine / analogs & derivatives*
  • Deoxycytidine / economics*
  • Docetaxel
  • Dose-Response Relationship, Drug
  • Female
  • Fluorouracil / analogs & derivatives
  • Follow-Up Studies
  • Humans
  • Neoplasm Metastasis
  • Ontario
  • Paclitaxel / administration & dosage*
  • Paclitaxel / analogs & derivatives*
  • Paclitaxel / economics*
  • Population Surveillance*
  • Survival Analysis
  • Taxoids*
  • Trastuzumab
  • Treatment Outcome
  • Vinblastine / administration & dosage
  • Vinblastine / analogs & derivatives*
  • Vinblastine / economics
  • Vinorelbine
  • Women's Health

Substances

  • Antibiotics, Antineoplastic
  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Humanized
  • Antimetabolites, Antineoplastic
  • Antineoplastic Agents, Phytogenic
  • Bridged-Ring Compounds
  • Taxoids
  • Deoxycytidine
  • Docetaxel
  • taxane
  • Vinblastine
  • Capecitabine
  • Trastuzumab
  • Paclitaxel
  • Vinorelbine
  • Fluorouracil