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Prediction of Pathologic Findings with MRI-Based Clinical Staging Using the Bayesian Network Modeling in Prostate Cancer: A Radiation Oncologist Perspective

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dc.contributor.authorWee, Chan Woo-
dc.contributor.authorJang, Bum-Sup-
dc.contributor.authorKim, Jin Ho-
dc.contributor.authorJeong, Chang Wook-
dc.contributor.authorKwak, Cheol-
dc.contributor.authorKim, Hyun Hoe-
dc.contributor.authorKu, Ja Hyeon-
dc.contributor.authorKim, Seung Hyup-
dc.contributor.authorCho, Jeong Yeon-
dc.contributor.authorKim, Sang Youn-
dc.date.accessioned2022-06-24T08:26:45Z-
dc.date.available2022-06-24T08:26:45Z-
dc.date.created2022-05-13-
dc.date.issued2022-01-
dc.identifier.citationCancer Research and Treatment, Vol.54 No.1, pp.234-244-
dc.identifier.issn1598-2998-
dc.identifier.urihttps://hdl.handle.net/10371/184078-
dc.description.abstractCopyright © 2022 by the Korean Cancer Association.Purpose This study aimed to develop a model for predicting pathologic extracapsular extension (ECE) and seminal vesicle invasion (SVI) while integrating magnetic resonance imaging-based T-staging (cTMRI, cT1c-cT3b). Materials and Methods A total of 1,915 who underwent radical prostatectomy between 2006-2016 met the inclusion/exclusion criteria. We performed a multivariate logistic regression analysis as well as Bayesian network (BN) modeling based on possible confounding factors. The BN model was internally validated using 5-fold validation. Results According to the multivariate logistic regression analysis, initial prostate-specific antigen (iPSA) (β=0.050, p < 0.001), percentage of positive biopsy cores (PPC) (β=0.033, p < 0.001), both lobe involvement on biopsy (β=0.359, p=0.009), Gleason score (β=0.358, p < 0.001), and cTMRI (β=0.259, p < 0.001) were significant factors for ECE. For SVI, iPSA (β=0.037, p < 0.001), PPC (β=0.024, p < 0.001), Gleason score (β=0.753, p < 0.001), and cTMRI (β=0.507, p < 0.001) showed statistical significance. BN models to predict ECE and SVI were also successfully established. The overall area under the receiver operating characteristic curve (AUC)/accuracy of the BN models were 0.76/73.0% and 0.88/89.6% for ECE and SVI, respectively. According to internal comparison between the BN model and Roach formula, BN model had improved AUC values for predicting ECE (0.76 vs. 0.74, p=0.060) and SVI (0.88 vs. 0.84, p < 0.001). Conclusion Two models to predict pathologic ECE and SVI integrating cTMRI were established and installed on a separate website for public access to guide radiation oncologists.-
dc.language영어-
dc.publisher대한암학회-
dc.titlePrediction of Pathologic Findings with MRI-Based Clinical Staging Using the Bayesian Network Modeling in Prostate Cancer: A Radiation Oncologist Perspective-
dc.typeArticle-
dc.identifier.doi10.4143/CRT.2020.1221-
dc.citation.journaltitleCancer Research and Treatment-
dc.identifier.wosid000792610700002-
dc.identifier.scopusid2-s2.0-85123614385-
dc.citation.endpage244-
dc.citation.number1-
dc.citation.startpage234-
dc.citation.volume54-
dc.identifier.kciidART002802703-
dc.description.isOpenAccessN-
dc.contributor.affiliatedAuthorJeong, Chang Wook-
dc.contributor.affiliatedAuthorKwak, Cheol-
dc.contributor.affiliatedAuthorKu, Ja Hyeon-
dc.contributor.affiliatedAuthorCho, Jeong Yeon-
dc.type.docTypeArticle-
dc.description.journalClass1-
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