The cost-effectiveness of prostate cancer screening using the Stockholm3 test

PLoS One. 2021 Feb 25;16(2):e0246674. doi: 10.1371/journal.pone.0246674. eCollection 2021.

Abstract

Objectives: The European Randomized Study of Screening for Prostate Cancer found that prostate-specific antigen (PSA) screening reduced prostate cancer mortality, however the costs and harms from screening may outweigh any mortality reduction. Compared with screening using the PSA test alone, using the Stockholm3 Model (S3M) as a reflex test for PSA ≥ 1 ng/mL has the same sensitivity for Gleason score ≥ 7 cancers while the relative positive fractions for Gleason score 6 cancers and no cancer were 0.83 and 0.56, respectively. The cost-effectiveness of the S3M test has not previously been assessed.

Methods: We undertook a cost-effectiveness analysis from a lifetime societal perspective. Using a microsimulation model, we simulated for: (i) no prostate cancer screening; (ii) screening using the PSA test; and (iii) screening using the S3M test as a reflex test for PSA values ≥ 1, 1.5 and 2 ng/mL. Screening strategies included quadrennial re-testing for ages 55-69 years performed by a general practitioner. Discounted costs, quality-adjusted life-years (QALYs) and incremental cost-effectiveness ratios (ICERs) were calculated.

Results: Comparing S3M with a reflex threshold of 2 ng/mL with screening using the PSA test, S3M had increased effectiveness, reduced lifetime biopsies by 30%, and increased societal costs by 0.4%. Relative to the PSA test, the S3M reflex thresholds of 1, 1.5 and 2 ng/mL had ICERs of 170,000, 60,000 and 6,000 EUR/QALY, respectively. The S3M test was more cost-effective at higher biopsy costs.

Conclusions: Prostate cancer screening using the S3M test for men with an initial PSA ≥ 2.0 ng/mL was cost-effective compared with screening using the PSA test alone.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Biomarkers, Tumor
  • Cost-Benefit Analysis
  • Early Detection of Cancer / economics*
  • Early Detection of Cancer / methods*
  • Early Detection of Cancer / trends
  • Humans
  • Kallikreins / analysis
  • Male
  • Middle Aged
  • Models, Statistical
  • Neoplasm Grading
  • Prostate-Specific Antigen / analysis
  • Prostatic Neoplasms / diagnosis*
  • Prostatic Neoplasms / economics
  • Prostatic Neoplasms / pathology
  • Randomized Controlled Trials as Topic
  • Risk Assessment
  • Sweden

Substances

  • Biomarkers, Tumor
  • KLK3 protein, human
  • Kallikreins
  • Prostate-Specific Antigen

Grants and funding

Funding was received from the Swedish Research Council (MC: 2018-02526, Swedish eScience Research Centre), Cancerfonden (MC: CAN 2018/539), NordForsk (MC: Nordic Information for Action eScience Center), Karolinska Institutet (MC: KID) and Prostatacancerförbundet (MC). AstraZeneca provided support in the form of salary for author AJ. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. The specific roles of these authors are articulated in the ‘author contributions’ section.