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Incidence and prognostic implications of PSA relapse after radical radiotherapy for prostate cancer: a population-based study
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences. IRCCS Osped San Raffaele, URI Inst, Unit Urol, Div Expt Oncol, Milan, Italy.ORCID iD: 0009-0005-8050-9388
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Urology.ORCID iD: 0000-0001-7181-7083
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Urology.ORCID iD: 0000-0002-8850-7863
Uppsala University, Disciplinary Domain of Medicine and Pharmacy, Faculty of Medicine, Department of Surgical Sciences, Urology.ORCID iD: 0000-0002-2404-5890
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2026 (English)In: BJU International, ISSN 1464-4096, E-ISSN 1464-410X, Vol. 137, no 4, p. 629-638Article in journal (Refereed) Published
Abstract [en]

Objective

To estimate risk of prostate-specific antigen (PSA) relapse after radical radiotherapy (RT) for prostate cancer (PCa), and risk of PCa death after relapse according to Gleason score and time to relapse.

Patients and Methods

Men in the National Prostate Cancer Register of Sweden who underwent primary radical RT in 2007–2024 were followed until 31 December 2024. Relapse was defined as a PSA level increase of ≥2 ng/mL above nadir (Phoenix criteria). Competing risk cumulative incidence analyses were used to estimate risk of PSA relapse and risk of PCa death after relapse according to Gleason score and time to relapse.

Results

The 10-year risk of relapse in 26 634 men treated with RT was 25% (95% confidence interval [CI] 24–25%). The 10-year risk of PCa death after relapse was 35% (95% CI 33–37%). In men with relapse after >3 years the risk was 18% for Gleason score 6 and 19% for Gleason score 3 + 4, while in men with a relapse within 18 months the risk was 52% for Gleason score 4 + 3 and 75% for Gleason score 9–10. In men with a relapse at 1 year after RT there was a four-fold higher risk of PCa death for men with Gleason score 9–10 compared to men with Gleason score 6 (86% vs 22%). In contrast, in men with a relapse at 10 years after RT there were little differences in risk of PCa death according to Gleason (14% vs 23%).

Conclusion

In this population-based study of RT for PCa, there was a wide range in the estimates of risk of PCa death after relapse in highly granular groups according to Gleason score and time to relapse. Notably, some estimates did not align with the European Association of Urology relapse risk group classification.

Place, publisher, year, edition, pages
John Wiley & Sons, 2026. Vol. 137, no 4, p. 629-638
Keywords [en]
prostate cancer, radical radiotherapy, prostate-specific antigen, relapse, biochemical recurrence, prostate cancer death
National Category
Cancer and Oncology
Identifiers
URN: urn:nbn:se:uu:diva-582325DOI: 10.1111/bju.70148ISI: 001708869900024PubMedID: 41537396Scopus ID: 2-s2.0-105027562129OAI: oai:DiVA.org:uu-582325DiVA, id: diva2:2046340
Part of project
Population-based studies in Prostate Cancer data Base Sweden (PCBaSe) EXTenD. Life expectancy and longterm effects of screening and treatment of prostate cancer in older men, Swedish Research Council
Funder
Region UppsalaSwedish Cancer Society, 2022-2051Available from: 2026-03-16 Created: 2026-03-16 Last updated: 2026-03-16Bibliographically approved

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Zaurito, PaoloGarmo, HansGedeborg, RolfAhlberg, MatsStattin, PärWesterberg, Marcus

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