Evidence map›Paper›PMID 41186967›Full record

ArticleJournal of magnetic resonance imaging : JMRI2026

Development and Deployment of a Machine Learning Model to Triage the Use of Prostate MRI (ProMT-ML) in Patients With Suspected Prostate Cancer.

Jesse Persily, Hersh Chandarana, Angela Tong, Rajesh Ranganath, Samir Taneja, Madhur Nayan

Abstract read
In one paragraph

Article in Journal of magnetic resonance imaging : JMRI, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. Review
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

6 authors.

Jesse PersilyDepartment of Urology, NYU Grossman School of Medicine, New York, New York, USA.
Hersh ChandaranaDepartment of Urology, NYU Grossman School of Medicine, New York, New York, USA.
Angela TongDepartment of Radiology, NYU Grossman School of Medicine, New York, New York, USA.ORCID https://orcid.org/0000-0002-4733-3414
Rajesh RanganathCourant Institute of Mathematical Sciences, New York University, New York, New York, USA.
Samir TanejaDepartment of Urology, NYU Grossman School of Medicine, New York, New York, USA.
Madhur NayanDepartment of Urology, NYU Grossman School of Medicine, New York, New York, USA.ORCID https://orcid.org/0000-0001-7502-3475

Funding

TR&D 4: Revealing Microstructure: Biophysical modeling and validation for discovery and clinical careP41EB017183 · NIBIB · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI Christopher M Collins · 2014 to 2026
$19.3M
NIBIB NIH HHS P41 EB017183
6 · The paper itself

Abstract

backgroundAccess to prostate MRI remains limited due to resource constraints and the need for expert interpretation. PURPOSE: To develop machine learning (ML) models that enable risk-based triage for prostate MRI (ProMT-ML) in the evaluation of prostate cancer. STUDY TYPE: Retrospective and prospective. POPULATION: A total of 11,879 retrospective MRI scans for suspected prostate cancer from a multi-hospital health system, divided into training (N = 9504) and test (N = 2375) sets. A total of 4551 records for prospective validation. FIELD STRENGTH/SEQUENCE: 1.5T and 3T/Turbo-spin echo T2-weighted imaging (T2WI), diffusion-weighted imaging (DWI), and dynamic contrast-enhanced (DCE). ASSESSMENT: Prostate Imaging Reporting and Data System (PI-RADS) scores were retrieved from MRI reports. The Boruta algorithm was used to select final input features from candidate features. Two models were developed using supervised ML to estimate the likelihood of an abnormal MRI, defined as PI-RADS ≥ 3: Model A (with prostate volume) and Model B (without prostate volume). Models were compared to PSA. Prostate biopsy pathology was assessed to evaluate potential clinical impact. STATISTICAL TESTS: Area under the receiver operating characteristic curve (AUC) was the primary performance metric.

resultsA total of 5580 (46.9%) subjects had a PI-RADS score ≥ 3. After feature selection, Model A included age, PSA, body mass index, and prostate volume, while Model B included age, PSA, body mass index, and systolic blood pressure. Both models A (AUC 0.711) and B (AUC 0.616) significantly outperformed PSA (AUC 0.593). Compared to PSA threshold > 4 ng/mL, Model A demonstrated significantly improved specificity (28.3% vs. 21.9%) and no significant difference in sensitivity (89.0% vs. 86.7%). Among false negatives (Model A: 8.0% (62/776); Model B: 16.8% (130/776)), most (Model A: 87%; Model B: 69%) had benign or clinically insignificant disease on biopsy. On prospective validation, both versions of ProMT-ML significantly outperformed PSA. DATA

conclusionProMT-ML provides personalized risk estimates of abnormal prostate MRI and can support triage of this test. LEVEL OF EVIDENCE: 2: TECHNICAL EFFICACY: Stage 4.

Indexed as

Machine LearningMagnetic Resonance ImagingProstatic NeoplasmsTriageAgedAlgorithmsContrast MediaHumansImage Interpretation, Computer-AssistedMaleMiddle AgedProspective StudiesProstateReproducibility of ResultsRetrospective StudiesROC CurveContrast Mediamachine learningprediction modelprostate cancerprostate MRIrisk‐stratificationtriage

Identifiers

PMID41186967
PMCPMC13032720

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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.