Assessment of harms, benefits, and cost-effectiveness of prostate cancer screening: A micro-simulation study of 230 scenarios

Cancer Med. 2020 Oct;9(20):7742-7750. doi: 10.1002/cam4.3395. Epub 2020 Aug 19.

Abstract

Background: Prostate cancer screening incurs a high risk of overdiagnosis and overtreatment. An organized and age-targeted screening strategy may reduce the associated harms while retaining or enhancing the benefits.

Methods: Using a micro-simulation analysis (MISCAN) model, we assessed the harms, benefits, and cost-effectiveness of 230 prostate-specific antigen (PSA) screening strategies in a Dutch population. Screening strategies were varied by screening start age (50, 51, 52, 53, 54, and 55), stop age (51-69), and intervals (1, 2, 3, 4, 8, and single test). Costs and effects of each screening strategy were compared with a no-screening scenario.

Results: The most optimum strategy would be screening with 3-year intervals at ages 55-64 resulting in an incremental cost-effectiveness ratio (ICER) of €19 733 per QALY. This strategy predicted a 27% prostate cancer mortality reduction and 28 life years gained (LYG) per 1000 men; 36% of screen-detected men were overdiagnosed. Sensitivity analyses did not substantially alter the optimal screening strategy.

Conclusions: PSA screening beyond age 64 is not cost-effective and associated with a higher risk of overdiagnosis. Similarly, starting screening before age 55 is not a favored strategy based on our cost-effectiveness analysis.

Keywords: harms and benefits; cost-effectiveness; micro-simulation; prostate cancer; prostate-specific antigen (PSA) screening.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Aged
  • Algorithms
  • Biomarkers, Tumor
  • Cost-Benefit Analysis
  • Early Detection of Cancer / economics
  • Early Detection of Cancer / methods
  • Humans
  • Male
  • Mass Screening / economics
  • Mass Screening / methods
  • Medical Overuse
  • Middle Aged
  • Models, Theoretical
  • Neoplasm Staging
  • Netherlands / epidemiology
  • Population Surveillance
  • Prostatic Neoplasms / diagnosis
  • Prostatic Neoplasms / epidemiology*
  • Prostatic Neoplasms / etiology

Substances

  • Biomarkers, Tumor