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The role of PSA density in the follow up of men with a negative MRI in the Göteborg-2 trial

Journal
BJU international (Q1)
Published
18 September 2026
Study design
Randomized controlled trial
Evidence level
Level 1, High (CEBM 1b)
Authors
Fredrik Möller, Marianne Månsson, Mikael Hellström, Fredrik Langkilde, Vasiliki Spyratou, Johan Stranne, et al.
PMID
42759951
DOI
10.1111/bju.70450

Why clinicians should know about it

  • Picked for Urology (top studies of the week, 25 October 2026): PSA density stratifies long‑term csPCa risk after negative MRI

Abstract

OBJECTIVES: To assess whether prostate-specific antigen density (PSAD) stratifies long-term risk of clinically significant prostate cancer (csPCa) after a negative magnetic resonance imaging (MRI; Prostate Imaging-Reporting and Data System score ≤2) and to evaluate the potential of PSAD to guide follow-up in a screening setting. PATIENTS AND METHODS: This pre-specified sub-analysis of the population-based, randomised Göteborg-2 screening trial included 1685 men who underwent PSA testing between October 2015 and June 2021 and had a subsequent negative initial MRI. Follow-up continued until 30 September 2024. The primary endpoint was cumulative incidence of csPCa (Gleason score ≥3 + 4). Men were categorised by baseline PSAD (<0.10, 0.10 to <0.15, and ≥0.15 ng/mL2). Cumulative incidence was estimated using Kaplan-Meier methods and compared using the log-rank test. The clinical implications of PSAD-based follow-up strategies were explored. RESULTS: Over a median follow-up of 5.5 years, 160 PCas were diagnosed, of which 80 were csPCa, including 22 cases of Gleason score ≥4 + 3. At 7 years, cumulative csPCa incidence was 7.1% overall and 5.5%, 13.8%, and 11.9% in the PSAD <0.10, 0.10 to <0.15, and ≥0.15 ng/mL2 groups, respectively (P < 0.001 for PSAD <0.10 ng/mL2 vs both higher groups). Overall, 87% of repeat MRIs remained negative. Although men with baseline PSAD <0.10 ng/mL2 had the lowest overall risk, 42 csPCas occurred in this group, including 12 Gleason score ≥4 + 3, emphasising the importance of continued regular PSA-based follow-up. A PSAD-guided strategy with biennial PSA testing and repeat MRI triggered by PSAD ≥0.10 ng/mL2 could reduce MRI use by 60% and biopsies by 46%, halve detection of clinically insignificant PCa, and delay csPCa diagnosis in 17% of cases including 10 men with Gleason score 3 + 4 and one with Gleason score ≥4 + 3. CONCLUSIONS: The PSAD stratifies long-term risk of csPCa after a negative MRI and supports risk-adapted follow-up in PCa screening.

Abstract as published, via PubMed.

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For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.