Swedish regional population-based organised prostate cancer testing: why, what and how?

Authors

  • Ola Bratt Department of Urology, Sahlgrenska University Hospital, Göteborg, Sweden
  • Salma Tunå Butt Department of Surgery, Skåne University Hospital, Lund University, Sweden
  • Charlotte Carlsson Regional Cancer Centre South East, Linköping, Sweden
  • Lisa Jelf-Eneqvist Regional Cancer Centre Stockholm-Gotland, Stockholm, Sweden
  • Olof Gunnarsson Department of Urology, Ryhov County Hospital, Jönköping, Sweden
  • Alma Ihre Regional Cancer Centre West, Gothenburg, Sweden
  • Thomas Jiborn Department of Urology, Helsingborg Hospital, Helsingborg, Sweden
  • Anna Lantz Department of Pelvic Cancer, Karolinska University Hospital, Stockholm, Sweden
  • Heide Larsson Regional Cancer Centre Mid-Sweden, Uppsala, Sweden
  • Helena Strömqvist Regional Cancer Centre North, Västerbotten County Council, Umeå, Sweden
  • Johan Styrke Regional Cancer Centre North, Västerbotten County Council, Umeå, Sweden
  • Nils-Erik Svedberg Regional Cancer Centre Mid-Sweden, Uppsala, Sweden
  • Rebecka Arnsrud Godtman Department of Urology, Sahlgrenska University Hospital, Göteborg, Sweden

DOI:

https://doi.org/10.2340/sju.v60.43809

Keywords:

Prostate cancer, organised testing, screening, population-based, diagnostics, quality control, performance indicators, review

Abstract

Objective: This study aimed to describe the regional, population-based, organised prostate cancer testing (OPT) programmes that are being introduced throughout Sweden: motives, structure, target population, diagnostic algorithm, quality control, outcomes, research, and future perspectives.

Results: In 2018, the Swedish National Board of Health and Welfare renewed their recommendation against screening for prostate cancer. Despite this, regional OPT was considered motivated to (1) improve cost-effectiveness compared with unorganised testing, (2) improve equity by giving every man in the target population a chance to make an informed choice, and (3) gain diagnostic and organisational knowledge. The OPT programmes are provided as a regional public healthcare service. They are coordinated by a national working group. The final target population is all men aged 50–74 years. Regional OPT offices use a national administrative system to organise all steps from sending invitation letters to prostate biopsy according to a strict diagnostic algorithm. General practice is involved for blood draw only or not at all. Data are registered in a national register (SweOPT); an annual report is published with the regions’ performance on key indicators. At the end of 2024, 16 of the 21 Swedish regions had started OPT and invited 256,000 men with an average cumulative participation rate of 43%. A consortium co-ordinates OPT-related research. A general experience is that communication and organisational matters have been more challenging than medical decisions.

Conclusions: The Swedish population-based OPT programmes provide organisational experiences, diagnostic outcomes, and research results of value for future national prostate cancer screening programmes.

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References

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Additional Files

Published

2025-06-03

How to Cite

Bratt, O., Butt, S. T., Carlsson, C., Jelf-Eneqvist, L., Gunnarsson, O., Ihre, A., … Arnsrud Godtman, R. (2025). Swedish regional population-based organised prostate cancer testing: why, what and how?. Scandinavian Journal of Urology, 60, 97–104. https://doi.org/10.2340/sju.v60.43809

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