Evidence map›Paper›PMID 40075601›Full record

ArticleCancers2025

A Simple Nomogram to Predict Clinically Significant Prostate Cancer at MRI-Guided Biopsy in Patients with Mild PSA Elevation and Normal DRE.

Hubert Kamecki, Andrzej Tokarczyk, Małgorzata Dębowska, Urszula Białończyk, Wojciech Malewski, Przemysław Szostek, Omar Tayara, Stefan Gonczar, Sławomir Poletajew, Łukasz Nyk and 2 more

Abstract read
In one paragraph

Article in Cancers, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

12 authors.

Hubert KameckiSecond Department of Urology, Centre of Postgraduate Medical Education, 01-809 Warsaw, Poland.
Andrzej TokarczykSecond Department of Urology, Centre of Postgraduate Medical Education, 01-809 Warsaw, Poland.
Małgorzata DębowskaNałęcz Institute of Biocybernetics and Biomedical Engineering, Polish Academy of Sciences, 02-109 Warsaw, Poland.
Urszula BiałończykNałęcz Institute of Biocybernetics and Biomedical Engineering, Polish Academy of Sciences, 02-109 Warsaw, Poland.
Wojciech MalewskiSecond Department of Urology, Centre of Postgraduate Medical Education, 01-809 Warsaw, Poland.
Przemysław SzostekSecond Department of Urology, Centre of Postgraduate Medical Education, 01-809 Warsaw, Poland.
Omar TayaraSecond Department of Urology, Centre of Postgraduate Medical Education, 01-809 Warsaw, Poland.
Stefan GonczarSecond Department of Urology, Centre of Postgraduate Medical Education, 01-809 Warsaw, Poland.
Sławomir PoletajewSecond Department of Urology, Centre of Postgraduate Medical Education, 01-809 Warsaw, Poland.ORCID 0000-0001-7664-9816
Łukasz NykSecond Department of Urology, Centre of Postgraduate Medical Education, 01-809 Warsaw, Poland.
Piotr KrystSecond Department of Urology, Centre of Postgraduate Medical Education, 01-809 Warsaw, Poland.
Stanisław SzemplińskiSecond Department of Urology, Centre of Postgraduate Medical Education, 01-809 Warsaw, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEvidence to help avoid unnecessary prostate biopsies is being actively pursued. Our goal was to develop and internally validate a nomogram for predicting clinically significant prostate cancer (csPC) in men with low suspicion of disease (prostate specific antigen [PSA] < 10 ng/mL, normal digital rectal examination [DRE]), in whom magnetic resonance imaging (MRI) findings are positive.

methodsPatients with no prior prostate cancer diagnosis who underwent MRI-ultrasound fusion biopsy of the prostate were retrospectively analyzed. Inclusion criteria were PSA < 10 ng/mL, normal DRE, Prostate Imaging Reporting And Data System (PIRADS) category ≥ 3, and no extraprostatic extension or seminal vesicle invasion reported on MRI. Associations between csPC diagnosis and patient or lesion characteristics were analyzed, and a multivariable model was developed. Internal validation of the model with 5-fold cross-validation and bootstrapping methods was performed.

resultsAmong 209 patients, 67 were diagnosed with csPC. Factors incorporated into the model for predicting csPC were age, 5-alpha reductase inhibitor use, PSA, prostate volume, PIRADS > 3, and lesion location in the peripheral zone. The model's ROC AUC was 0.86, with consistent performance at internal validation (0.84 with cross-validation, 0.82 with bootstrapping). With an empirical threshold of <10% csPC probability to omit biopsy, 72 (50.7%) unnecessary biopsies would have been avoided, at the cost of missing 2 (3.0%) csPC cases.

conclusionsOur nomogram might serve as a valuable tool in refining selection criteria in men considered for prostate biopsy. The major limitation of the study is its retrospective character. Prospective, external validation of the model is warranted.

Indexed as

csPCfusion biopsynomogramprostate cancer

Identifiers

PMID40075601
PMCPMC11898869

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