Evidence map›Paper›PMID 40415146›Full record

ArticleInternational urology and nephrology2025

Predictive clinical characteristics for adverse pathological outcomes in intermediate- and high-risk prostate cancer during biopsy.

Miroslav Stojadinovic, Nebojsa Jurisevic, Milorad Stojadinovic, Slobodan Jankovic

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

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0cells of the map it votes in
1citing papers 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

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Miroslav StojadinovicFaculty of Medical Sciences, University of Kragujevac, SvetozaraMarkovica 69, 34 000, Kragujevac, Serbia. midinac@gmail.com.ORCID http://orcid.org/0000-0002-5215-8729
Nebojsa JurisevicFaculty of Engineering, University of Kragujevac, Kragujevac, Serbia.ORCID http://orcid.org/0000-0002-1609-6313
Milorad StojadinovicClinic for Nephrology, University Clinical Center of Serbia, Belgrade, Serbia.ORCID http://orcid.org/0000-0002-1332-6961
Slobodan JankovicFaculty of Medical Sciences, Pharmacology and Toxicology Department, University of Kragujevac, Kragujevac, Serbia.ORCID http://orcid.org/0000-0002-1519-8828

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeAdverse pathological features in prostate cancer (PCa) are characteristics found in biopsy tissue that indicate a more aggressive or advanced disease. This study aims to develop a biopsy-based model for assessing the risk of adverse PCa and to evaluate its performance against the European Randomized Study of Screening for Prostate Cancer (ERSPC) Risk Calculator (RC) 3/4 and PSA models.

methodsBetween January 2017 and December 2022, patients with prostate-specific antigen (PSA) levels of ≤ 50 ng/mL underwent prostate biopsies. The patients' age, PSA, digital rectal exam, prostate volume, PSA density (PSAD), previous negative biopsy, number of positive cores, Gleason score, and biopsy outcomes were documented. Patients were classified into categories: no cancer, very low-risk, low-risk, intermediate-risk, and high-risk groups. We investigated the relationship between our model and adverse PCa using a binary Generalized Linear Model (GLM). We evaluated the model's discriminatory ability using the area under the receiver operating characteristic curve (AUC) and compared its predictive performance with the adverse model in terms of discrimination, calibration, and clinical utility.

resultsOut of 824 patients, PCa was diagnosed in 320 (38.8%) men, and 203 (24.6%) had unfavorable PCa. The GLM demonstrated improved performance metrics, with an AUC of 0.766, compared to 0.639 for the RC 3/4 model and 0.655 for the PSA model. The GLM showed a good fit and provided a greater net benefit.

conclusionThe study identified clinical predictors of adverse PCa during biopsy, demonstrating moderate discrimination and clinical utility. Further large multicenter studies are required for validation.

Indexed as

ProstateProstatic NeoplasmsAgedBiopsyHumansMaleMiddle AgedPredictive Value of TestsProstate-Specific AntigenRetrospective StudiesRisk AssessmentProstate-Specific AntigenHigh riskProstate biopsyProstate cancerProstate voluRisk factors

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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.