Evidence map›Paper›PMID 40739907›Full record

ArticleThe British journal of radiology2025

Reevaluating prostate imaging-reporting and data system 3 lesions upgraded to 4: the emergence of a new subgroup?

Diğdem Kuru Öz, Sezer Nil Yılmazer Zorlu, Zeynep Eskalen, Nuray Haliloğlu, Ayşe Erden

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Article in The British journal of radiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Diğdem Kuru ÖzDepartment of Radiology, School of Medicine, Ankara University, 06230 Ankara, Turkey.ORCID 0000-0001-8873-3476
Sezer Nil Yılmazer ZorluDepartment of Radiology, Ankara Mamak State Hospital, 06270 Ankara, Turkey.ORCID 0009-0001-7162-4668
Zeynep EskalenDepartment of Radiology, Tunceli State Hospital, 62000 Tunceli, Turkey.ORCID 0000-0001-7671-5131
Nuray HaliloğluDepartment of Radiology, School of Medicine, Ankara University, 06230 Ankara, Turkey.ORCID 0000-0002-1125-4896
Ayşe ErdenDepartment of Radiology, School of Medicine, Ankara University, 06230 Ankara, Turkey.ORCID 0000-0002-9518-5428

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesThe study aims to evaluate Prostate Imaging-Reporting and Data System 4 (PI-RADS 4) lesions, including those with primary diffusion restriction (diffusion-weighted imaging score 4) and those upgraded from PI-RADS 3 due to positive dynamic contrast-enhanced findings, and to compare outcomes between these groups while also assessing cancer detection rates and prostatitis between upgraded cases and PI-RADS 3 lesions.

methodsIn this single-center cohort study, peripheral zone lesions classified as PI-RADS 3 and 4 by multiparametric MRI and biopsied via MRI/transrectal ultrasound-guided targeted biopsy were analyzed.

resultsOf 420 peripheral zone lesions from 272 patients, 202 were PI-RADS 3, 81 PI-RADS 3 + 1, and 137 PI-RADS 4. Cancer detection rates significantly differed between PI-RADS 3 + 1 and PI-RADS 4 (38.3% vs 73% for overall cancer; 6.2% vs 30.7% for clinically significant cancer, P < .001). PI-RADS 3 + 1 lesions had significantly higher cancer detection rates than PI-RADS 3 lesions (38.3% vs 19.8%, P  = .001). Prostatitis was significantly more prevalent in PI-RADS 3 (34.7%) and PI-RADS 3 + 1 (29.6%) than in PI-RADS 4 (10.9%) lesions (P < .001).

conclusionsPI-RADS 3 + 1 lesions show significantly different cancer detection rates from both PI-RADS 3 and 4, suggesting they should be managed as a distinct entity. Higher prevalence of prostatitis in PI-RADS 3 + 1 lesions indicates that clinical evaluation for inflammatory conditions may help reduce unnecessary biopsies in this subgroup. ADVANCES IN KNOWLEDGE: PI-RADS 3 + 1 lesions show higher cancer detection than PI-RADS 3 but lower than PI-RADS 4, and are more frequently associated with prostatitis than PI-RADS 4. These findings support individualized management to avoid unnecessary biopsies.

Indexed as

Prostatic NeoplasmsAgedCohort StudiesDiffusion Magnetic Resonance ImagingHumansImage-Guided BiopsyMaleMiddle AgedMultiparametric Magnetic Resonance ImagingProstateProstatitisRadiology Information SystemsRetrospective StudiesMRI-targeted biopsymulti-parametric prostate magnetic resonance ımagingPI-RADSprostate cancer

Identifiers

PMID40739907
PMCPMC12515037

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.