Cost-utility analysis of genetic polymorphism universal screening in colorectal cancer prevention by detection of high-risk individuals

Dig Liver Dis. 2019 Dec;51(12):1731-1737. doi: 10.1016/j.dld.2019.07.012. Epub 2019 Aug 14.

Abstract

Background: In the past 15 years numerous studies have been published on the involvement of low-penetrance susceptibility genes on the risk for developing colorectal cancer (CRC).

Aim: To perform an economic analysis of blood genetic testing in CRC screening in a population-based nationwide setting using polymorphisms in prostaglandin E2 pathway genes as proof of concept.

Methods: A cost-utility analysis was performed from a societal perspective in Portugal comparing two strategies: blood genetic testing by the age of 40 versus no genetic screening under different assumptions of the cost of genetic testing (€10 and €30) and expected risk (1.5 to 5-fold). The adopted threshold was set at €44,870 (USD 50,000). The primary outcome was the incremental cost-effectiveness ratio (ICER) for a base case scenario.

Results: Polymorphism genotyping provided cost-utility only under the assumption of a 5-fold increased risk in the general population, providing ICERs of €44,356 and €30,389 for €30 and €10 tests, respectively.

Conclusion: Blood genetic screening for colorectal cancer has cost-utility only under specific assumptions of increased CRC risk and conservative cost estimates. Future studies should focus on defining genetic profiles because single-gene approaches are very unlikely to be cost-effective considering their modest predictive value.

Keywords: Colorectal cancer; Cost analysis; Cost-benefit analysis; Genetic polymorphisms.

MeSH terms

  • Adult
  • Colorectal Neoplasms* / diagnosis
  • Colorectal Neoplasms* / genetics
  • Colorectal Neoplasms* / prevention & control
  • Cost-Benefit Analysis
  • Cyclooxygenase 2 / metabolism*
  • Dinoprostone / metabolism*
  • Early Detection of Cancer* / economics
  • Early Detection of Cancer* / methods
  • Female
  • Genetic Predisposition to Disease
  • Genetic Testing* / economics
  • Genetic Testing* / methods
  • Humans
  • Male
  • Polymorphism, Single Nucleotide
  • Portugal
  • Proof of Concept Study
  • Risk Assessment / methods
  • Signal Transduction / genetics*

Substances

  • Cyclooxygenase 2
  • Dinoprostone