Cost-effectiveness of treatments for HER2-positive metastatic breast cancer and associated metastases: an overview of systematic reviews

Expert Rev Pharmacoecon Outcomes Res. 2021 Jun;21(3):353-364. doi: 10.1080/14737167.2021.1848553. Epub 2020 Dec 1.

Abstract

Introduction: Treatment of human epithelial growth factor receptor 2 (HER2)-positive breast cancer has rapidly evolved over the past decades with the addition of trastuzumab, lapatinib, pertuzumab, and trastuzumab emtansine (T-DM1). These treatments have dramatically impacted the survival of HER2-positive metastatic breast cancer (mBC) patients. Nonetheless, these agents are associated with high price tags, begging the question, 'Are treatments for HER2-positive metastatic breast cancer and associated metastases cost-effective'?Areas covered: We examine evidence on the cost-effectiveness of treatments for HER2-positive metastatic breast cancer and associated metastases through a review of systematic reviews on the topic. Additionally, we discuss the implications of our findings and provide recommendations for future directions in the assessment of the cost-effectiveness of targeted directed agents for HER2-positive mBC.Expert opinion: Heterogeneous evidence from cost-effectiveness studies on the use of targeted directed agents for HER2-positive mBC across the world caution against cross-country comparisons of the value of such treatments. It also militates in favor of the production and use of cost-effectiveness analyses for local rather than global decision-making, thus ensuring that economic evaluations reflect the needs of local decision-makers and populations for which they are devised.

Keywords: Breast cancer; cost-effectiveness; her2-positive receptors; metastases; systematic review.

Publication types

  • Review

MeSH terms

  • Antineoplastic Agents / administration & dosage*
  • Antineoplastic Agents / economics
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / economics
  • Cost-Benefit Analysis
  • Female
  • Humans
  • Molecular Targeted Therapy*
  • Neoplasm Metastasis
  • Receptor, ErbB-2 / metabolism
  • Survival Rate
  • Systematic Reviews as Topic

Substances

  • Antineoplastic Agents
  • ERBB2 protein, human
  • Receptor, ErbB-2