A systematic review of economic evaluations of tyrosine kinase inhibitors for non-small cell lung cancer (NSCLC)

Expert Opin Pharmacother. 2022 Aug;23(11):1247-1257. doi: 10.1080/14656566.2022.2095203. Epub 2022 Jul 4.

Abstract

Introduction: Although tyrosine kinase inhibitors (TKIs) have improved the efficacy of treatment for non-small cell lung cancer (NSCLC), the accessibility of TKIs is limited due to high costs. Despite the critical role of the cost-effectiveness of TKIs on decision-making, no systematic reviews have compared the cost-effectiveness of comparable TKIs. Therefore, we systemically reviewed the economic evaluation studies on various TKIs for NSCLC.

Areas covered: We searched PubMed and the Cochran Library to identify the published economic evaluation studies of TKIs in NSCLC patients that were published by January 2022. All of the included studies (n = 38) evaluated the cost-effectiveness of epidermal growth factor receptor (EGFR)-TKIs (n = 29) or anaplastic lymphocyte kinase (ALK)-TKIs (n = 9). The cost-effectiveness results were reported as the incremental cost-effectiveness ratio per quality-adjusted life-year, except for three studies.

Expert opinion: We found that the economic evaluation studies of the first and second generation of EGFR-TKIs and ALK-TKIs varied by the country and study settings, such as comparator and input parameters. In 12 studies, osimertinib (EGFR-TKI) was not cost-effective compared to other first/second EGFR-TKIs, regardless of the study settings. More evidence can be provided about cost-effectiveness of the third-generation TKIs in future research.

Keywords: Non-small cell lung cancer; cost-effectiveness analysis; economic evaluation; systematic review; tyrosine kinase inhibitor.

Publication types

  • Systematic Review

MeSH terms

  • Anaplastic Lymphoma Kinase / antagonists & inhibitors
  • Carcinoma, Non-Small-Cell Lung* / drug therapy
  • Carcinoma, Non-Small-Cell Lung* / economics
  • Cost-Benefit Analysis
  • ErbB Receptors / antagonists & inhibitors
  • Humans
  • Lung Neoplasms* / drug therapy
  • Lung Neoplasms* / economics
  • Mutation
  • Protein Kinase Inhibitors* / economics
  • Protein Kinase Inhibitors* / therapeutic use
  • Protein-Tyrosine Kinases / antagonists & inhibitors

Substances

  • Protein Kinase Inhibitors
  • ALK protein, human
  • Anaplastic Lymphoma Kinase
  • EGFR protein, human
  • ErbB Receptors
  • Protein-Tyrosine Kinases