Evidence map›Paper›PMID 42641045›Full record

ArticleThe Prostate2026

Natural History of PI-RADS 3 Lesions on Serial Prostate mpMRI.

Tomer Bashi, Yanai Rubinstein, Adi Kidron, Ron Marom, Yuval Rand, Meitar Atias, Sophie Barnes, Ibrahim Fahoum, Gal Keren-Paz, Mario Sofer and 4 more

Abstract read
In one paragraph

Article in The Prostate, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

14 authors.

Tomer BashiDepartment of Urology, Tel Aviv Sourasky Medical Center, Tel Aviv-Yafo, Israel.ORCID https://orcid.org/0000-0001-5054-6536
Yanai RubinsteinDepartment of Urology, Tel Aviv Sourasky Medical Center, Tel Aviv-Yafo, Israel.
Adi KidronDepartment of Urology, Tel Aviv Sourasky Medical Center, Tel Aviv-Yafo, Israel.
Ron MaromDepartment of Urology, Tel Aviv Sourasky Medical Center, Tel Aviv-Yafo, Israel.ORCID https://orcid.org/0000-0003-2137-1057
Yuval RandDepartment of Urology, Tel Aviv Sourasky Medical Center, Tel Aviv-Yafo, Israel.
Meitar AtiasDepartment of Urology, Tel Aviv Sourasky Medical Center, Tel Aviv-Yafo, Israel.
Sophie BarnesGray Faculty of Medicine, Tel Aviv University, Tel Aviv-Yafo, Israel.
Ibrahim FahoumGray Faculty of Medicine, Tel Aviv University, Tel Aviv-Yafo, Israel.
Gal Keren-PazDepartment of Urology, Tel Aviv Sourasky Medical Center, Tel Aviv-Yafo, Israel.
Mario SoferDepartment of Urology, Tel Aviv Sourasky Medical Center, Tel Aviv-Yafo, Israel.ORCID https://orcid.org/0000-0001-9346-0871
Ofer YossepowitchDepartment of Urology, Tel Aviv Sourasky Medical Center, Tel Aviv-Yafo, Israel.
Snir DekaloDepartment of Urology, Tel Aviv Sourasky Medical Center, Tel Aviv-Yafo, Israel.ORCID https://orcid.org/0000-0001-8031-9684
Avi BeriDepartment of Urology, Tel Aviv Sourasky Medical Center, Tel Aviv-Yafo, Israel.
Roy ManoDepartment of Urology, Tel Aviv Sourasky Medical Center, Tel Aviv-Yafo, Israel.ORCID https://orcid.org/0000-0003-3855-0211

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivePI-RADS 3 lesions on prostate multiparametric MRI (mpMRI) are indeterminate findings with debated management. We evaluated their radiologic evolution on follow-up mpMRI and correlated imaging changes with biopsy outcomes.

methodsWe retrospectively identified 166 men with at least one PI-RADS 3 lesion on initial mpMRI and at least one follow-up mpMRI without intervening treatment. Lesions were classified at follow-up as regressed (downgraded to PI-RADS ≤ 2), stable (remained PI-RADS 3), or progressed (upgraded to PI-RADS 4-5). Lesions were stratified by zonal location. MRI-targeted biopsy results were reviewed when available (n = 64).

resultsOn follow-up, 52% of lesions regressed, 29% remained stable, and 19% progressed. Progression was significantly more common for peripheral-zone lesions (25%) than transition-zone lesions (6%); no central-zone lesions progressed. Of the biopsied lesions, most yielded benign or low-grade pathology: 44% were benign, 47% were ISUP 1, 6% had high-grade PIN or ASAP, and only 3% harbored clinically significant prostate cancer (csPCa; ISUP ≥ 2). Both csPCa cases occurred in lesions that had progressed radiologically. Lesions with imaging progression were significantly more likely to yield cancer on initial or follow-up biopsy than stable/regressed lesions (83% vs 40%; p = 0.037).

conclusionsIn this real-world cohort, most PI-RADS 3 lesions remained indolent: over half regressed, and 19% progressed. Biopsied lesions had a very low rate of csPCa (3%). These results suggest that surveillance with interval MRI rather than immediate biopsy may be a safe strategy for selected men with PI-RADS 3 lesions.

Indexed as

Multiparametric Magnetic Resonance ImagingProstateProstatic NeoplasmsAgedDisease ProgressionFollow-Up StudiesHumansImage-Guided BiopsyMaleMiddle AgedRetrospective StudiesMRI surveillancemultiparametric MRIPI‐RADSprostate cancer detectionprostate MRI

Identifiers

PMID42641045
PMCPMC13656325

What OpenQuestion holds

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Registered trials

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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.