Optimal threshold of the prostate health index in predicting aggressive prostate cancer using predefined cost-benefit ratios and prevalence.


Journal

International urology and nephrology
ISSN: 1573-2584
Titre abrégé: Int Urol Nephrol
Pays: Netherlands
ID NLM: 0262521

Informations de publication

Date de publication:
May 2020
Historique:
received: 10 10 2019
accepted: 16 12 2019
pubmed: 26 12 2019
medline: 2 3 2021
entrez: 26 12 2019
Statut: ppublish

Résumé

The aim of the study was to determine optimal threshold of the Prostate Health Index (Phi) for predicting aggressive prostate cancer (PCa), taking into account misclassification costs, prevalence, and plausible risk factors. This prospective cohort study analyzed patients undergoing prostate biopsy and Phi testing. The primary endpoint was aggressive PCa, defined as biopsy Gleason score ≥ 7. The data about age, total prostate-specific antigen (PSA), percentage of free PSA (%fPSA), and digital rectal examination (DRE) were extracted from the patient files. We divided the patients to the low- and high-risk group. The clinical usefulness of the Phi was assessed by the decision curve analysis. The predictive performance was assessed using the area under the receiver operating characteristic curve (AUC), per-class metrics, and the potential reduction in unnecessary biopsies. The uncertain interval of Phi values was also determined. There were 200 men included in the study, 35 (17.5%) of them having aggressive PCa. Important predictors of aggressive PCa were %fPSA, DRE, Phi, and belonging to the high-risk group. With optimal threshold of 30.7, about 32% unnecessary biopsies would be avoided. The optimal threshold of Phi was lower in the high-risk group than in the low-risk group. The AUC for detection of aggressive PCa was 0.791. Per-class metrics showed that the Phi has insufficient diagnostic accuracy. The lower and upper limits of the uncertain interval were 41.8 and 51.4, respectively. Different thresholds of the Phi could be optimal, depending on prevalence, patient characteristics, and misclassification costs. Further studies with a larger patient sample are necessary to confirm our conclusions.

Identifiants

pubmed: 31875279
doi: 10.1007/s11255-019-02367-z
pii: 10.1007/s11255-019-02367-z
doi:

Substances chimiques

(-2)pro-prostate-specific antigen, human 0
Protein Precursors 0
KLK3 protein, human EC 3.4.21.-
Kallikreins EC 3.4.21.-
Prostate-Specific Antigen EC 3.4.21.77

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

893-901

Auteurs

Miroslav Stojadinovic (M)

Department of Urology, Clinic of Urology and Nephrology, Clinical Centre "Kragujevac", Zmaj Jovina 30, 34 000, Kragujevac, Serbia. midinac@gmail.com.
Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia. midinac@gmail.com.

Ivan Vukovic (I)

Clinic of Urology, Clinical Center of Serbia, University of Belgrade, Belgrade, Serbia.

Milos Ivanovic (M)

Department of Mathematics and Informatics, Faculty of Science, University of Kragujevac, Kragujevac, Serbia.

Milorad Stojadinovic (M)

Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia.

Dragan Milovanovic (D)

Pharmacology and Toxicology Department, Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia.

Damnjan Pantic (D)

Department of Urology, Clinic of Urology and Nephrology, Clinical Centre "Kragujevac", Zmaj Jovina 30, 34 000, Kragujevac, Serbia.

Slobodan Jankovic (S)

Pharmacology and Toxicology Department, Faculty of Medical Sciences, University of Kragujevac, Kragujevac, Serbia.

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Classifications MeSH