Evidence map›Paper›PMID 42806037›Full record

ArticleEuropean radiology2026

Clinical and MRI characteristics of germline pathogenic variant carriers diagnosed with prostate cancer.

Rory L Cochran, Madhangi Parameswaran, Nabih Nakrour, Soumyadeep Ghosh, Abdelrahman Elshikh, Miraj Rawal, Maximillian Pohl, Nuttaphon Aleenajitpong, Onofrio A Catalano, Amirkasra Mojtahed and 4 more

Abstract read
PubMed Publisher
In one paragraph

Article in European radiology, 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.

Rory L Cochran *Department of Radiology, Massachusetts General Hospital, Mass General Brigham, Boston, MA, USA. rcochran@mgh.harvard.edu.ORCID http://orcid.org/0000-0001-9123-4010
Madhangi Parameswaran *Department of Radiology, Massachusetts General Hospital, Mass General Brigham, Boston, MA, USA.
Nabih NakrourDepartment of Radiology, Massachusetts General Hospital, Mass General Brigham, Boston, MA, USA.
Soumyadeep GhoshDepartment of Radiology, Massachusetts General Hospital, Mass General Brigham, Boston, MA, USA.
Abdelrahman ElshikhDepartment of Radiology, Massachusetts General Hospital, Mass General Brigham, Boston, MA, USA.
Miraj RawalDepartment of Radiology, Massachusetts General Hospital, Mass General Brigham, Boston, MA, USA.
Maximillian PohlDepartment of Radiology, Massachusetts General Hospital, Mass General Brigham, Boston, MA, USA.
Nuttaphon AleenajitpongDepartment of Radiology, Massachusetts General Hospital, Mass General Brigham, Boston, MA, USA.
Onofrio A CatalanoDepartment of Radiology, Massachusetts General Hospital, Mass General Brigham, Boston, MA, USA.
Amirkasra MojtahedDepartment of Radiology, Massachusetts General Hospital, Mass General Brigham, Boston, MA, USA.
Shelley R McCormickMass General Brigham Cancer Institute, Boston, MA, USA.
Linda H Rodgers-FoucheMass General Brigham Cancer Institute, Boston, MA, USA.
Mukesh G HarisinghaniDepartment of Radiology, Massachusetts General Hospital, Mass General Brigham, Boston, MA, USA.ORCID http://orcid.org/0000-0003-0993-1947
Keyan SalariHarvard Medical School, Boston, MA, USA.ORCID http://orcid.org/0000-0001-7940-4558

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesCompare the clinical and imaging features of prostate cancer (PCa) patients harboring a germline pathogenic variant (PV) to sporadic controls. MATERIALS AND

methodsA single-center retrospective case-control study was performed by identifying patients with positive germline genetic testing for a PV diagnosed with prostate cancer between December 2015 and October 2025. Clinical, pathologic, and MRI characteristics of PV carriers were compared to a control group of consecutive patients diagnosed with PCa over 1 year. Mann-Whitney U-test was used for continuous data and Fisher's exact test for categorical comparisons.

resultsA total of 62 patients with PCa harboring ≥ 1 PV and an MRI at diagnosis were compared to 246 controls. The most frequent genes were Lynch syndrome (LS) associated (17.7%), CHEK2 (21.0%), ATM (17.7%), and BRCA2 (19.4%). Median age of PV carriers was not significantly younger than controls at diagnosis (65 years [IQR, 58-71], vs 67 years [61-73], p = 0.05). The proportion of patients with a positive MRI (PI-RADS ≥ 3) did not differ between groups (98% PV vs 96% control, p = 0.70). PV carriers were more likely to receive a PI-RADS 5 score (OR: 2.7; CI: 1.5-4.9, p < 0.01) and grade 3 extra-prostatic extension (OR: 3.0; CI: 1.5-5.8, p < 0.01). At prostatectomy, the proportion of patients reclassified to a higher-grade group was larger for PV carriers (37% vs 20%, p = 0.046).

conclusionPV carriers with PCa tend to manifest more aggressive imaging findings and are more likely to experience pathologic upgrading at prostatectomy. KEY POINTS: Question Differences in the clinical and imaging characteristics of sporadic prostate cancer (PCa) patients compared to patients harboring a PCa-associated germline pathogenic variant remain understudied. Findings PV carriers with PCa manifest more aggressive imaging features and are more likely to demonstrate pathologic upgrading at prostatectomy. Clinical relevance Knowledge of the unique clinical and imaging manifestations of hereditary PCa should support ongoing early detection studies and underscore the need for radiologists to be familiar with patient-centered early detection strategies utilizing MRI.

Indexed as

Hereditary prostate cancerMagnetic resonance imagingProstate cancerProstate-specific antigen

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.