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A Novel Machine Learning-based Predictive Model of Clinically Significant Prostate Cancer and Online Risk Calculator

dc.contributor.authorVasconcelos Ordones, Flavio [UNESP]
dc.contributor.authorKawano, Paulo Roberto [UNESP]
dc.contributor.authorVermeulen, Lodewikus
dc.contributor.authorHooshyari, Ali
dc.contributor.authorScholtz, David
dc.contributor.authorGilling, Peter John
dc.contributor.authorForeman, Darren
dc.contributor.authorKaufmann, Basil
dc.contributor.authorPoyet, Cedric
dc.contributor.authorGorin, Michael
dc.contributor.authorBarbosa, Abner Macola Pacheco [UNESP]
dc.contributor.authorda Rocha, Naila Camila [UNESP]
dc.contributor.authorde Andrade, Luis Gustavo Modelli [UNESP]
dc.contributor.institutionTauranga Public Hospital
dc.contributor.institutionUniversity of Auckland
dc.contributor.institutionUniversidade Estadual Paulista (UNESP)
dc.contributor.institutionFlinders University
dc.contributor.institutionUniversity Hospital of Zurich
dc.contributor.institutionIcahn School of Medicine at Mount Sinai
dc.date.accessioned2025-04-29T20:08:20Z
dc.date.issued2025-02-01
dc.description.abstractObjective: To create a machine-learning predictive model combining prostate imaging-reporting and data system (PI-RADS) score, PSA density, and clinical variables to predict clinically significant prostate cancer (csPCa). Methods: We evaluated a cohort of patients who underwent prostate biopsy for suspected prostate cancer (PCa) in New Zealand, Australia, and Switzerland. We collected data on age, body mass index (BMI), PSA level, prostate volume, PSA density (PSAD), PI-RADS scores, previous biopsy, and corresponding histology results. The dataset was divided into derivation (training) and validation (test) sets using random splits. An independent dataset was obtained from the Harvard Dataverse for external validation. A cohort of 1272 patients was analyzed. We fitted a Lasso model, XGBoost, and LightGBM to the training set and assessed their accuracy. Results: All models demonstrated ROC-AUC values ranging from 0.830 to 0.851. LightGBM was considered the superior model, with an ROC of 0.851 (95%CI: 0.804-0.897) in the test set and 0.818 (95% CI: 0.798-0.831) in the external dataset. The most important variable was PI-RADS, followed by PSA density, history of previous biopsy, age, and BMI. Conclusion: We developed a predictive model for detecting csPCa that exhibited a high ROC-AUC value for internal and external validations. This suggests that the integration of the clinical parameters outperformed each individual predictor. Additionally, the model demonstrated good calibration metrics, indicative of a more balanced model than the existing models.en
dc.description.affiliationTauranga Public Hospital, Bay of Plenty
dc.description.affiliationUniversity of Auckland
dc.description.affiliationUrology Department UNESP São Paulo State University, SP
dc.description.affiliationCollege of Medicine and Public Health Flinders University
dc.description.affiliationDepartment of Urology University Hospital of Zurich
dc.description.affiliationDepartment of Urology Icahn School of Medicine at Mount Sinai
dc.description.affiliationDepartment of Internal Medicine UNESP São Paulo State University, SP
dc.description.affiliationUnespUrology Department UNESP São Paulo State University, SP
dc.description.affiliationUnespDepartment of Internal Medicine UNESP São Paulo State University, SP
dc.format.extent20-26
dc.identifierhttp://dx.doi.org/10.1016/j.urology.2024.11.001
dc.identifier.citationUrology, v. 196, p. 20-26.
dc.identifier.doi10.1016/j.urology.2024.11.001
dc.identifier.issn1527-9995
dc.identifier.issn0090-4295
dc.identifier.scopus2-s2.0-85210965917
dc.identifier.urihttps://hdl.handle.net/11449/307058
dc.language.isoeng
dc.relation.ispartofUrology
dc.sourceScopus
dc.titleA Novel Machine Learning-based Predictive Model of Clinically Significant Prostate Cancer and Online Risk Calculatoren
dc.typeArtigopt
dspace.entity.typePublication

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