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<dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:invenio="http://invenio-software.org/elements/1.0" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd"><dc:identifier>doi:10.3390/cancers14205100</dc:identifier><dc:language>eng</dc:language><dc:creator>Morote, Juan</dc:creator><dc:creator>Borque Fernando, Ángel</dc:creator><dc:creator>Triquell, Marina</dc:creator><dc:creator>Campistol, Miriam</dc:creator><dc:creator>Celma, Anna</dc:creator><dc:creator>Regis, Lucas</dc:creator><dc:creator>Abascal, José M.</dc:creator><dc:creator>Servian, Pol</dc:creator><dc:creator>Planas, Jacques</dc:creator><dc:creator>Mendez, Olga</dc:creator><dc:creator>Esteban, Luis M.</dc:creator><dc:creator>Trilla, Enrique</dc:creator><dc:title>A clinically significant prostate cancer predictive model using digital rectal examination prostate volume category to stratify initial prostate cancer suspicion and reduce magnetic resonance imaging demand</dc:title><dc:identifier>ART-2022-130629</dc:identifier><dc:description>A predictive model including age, PCa family history, biopsy status (initial vs repeat), DRE (normal vs abnormal), serum prostate-specific antigen (PSA), and DRE prostate volume ca-tegory was developed to stratify initial PCa suspicion in 1486 men with PSA &amp;gt; 3 ng/mL and/or abnormal DRE, in whom mpMRI followed; 2- to 4-core TRUS-guided biopsies where Prostate Imaging Report and Data System (PI-RADS) &amp;gt; 3 lesions and/or 12-core TRUS systematic biopsies were performed in one academic institution between 1 January 2016–31 December 2019. The csPCa detection rate, defined as International Society of Uro-Pathology grade group 2 or higher, was 36.9%. An external validation of designed BCN-RC 1 was carried out on 946 men from two other institutions in the same metropolitan area, using the same criteria of PCa suspicion and diagnostic approach, yielded a csPCa detection rate of 40.8%. The areas under the receiver operating characteristic curves of BCN-RC 1 were 0.823 (95% CI: 0.800–0.846) in the development cohort and 0.837 (95% CI: 0.811–0.863) in the validation cohort (p = 0.447). In both cohorts, BCN-RC 1 exhibited net benefit over performing mpMRI in all men from 8 and 12% risk thresholds, respectively. At 0.95 sensitivity of csPCa, the specificities of BCN-RC 1 were 0.24 (95% CI: 0.22–0.26) in the development cohort and 0.34 (95% CI: 0.31–0.37) in the validation cohort (p &amp;lt; 0.001). The percentages of avoided mpMRI scans were 17.2% in the development cohort and 22.3% in the validation cohort, missing between 1.8% and 2% of csPCa among men at risk of PCa. In summary, BCN-RC 1 can stratify initial PCa suspicion, reducing the demand of mpMRI, with an acceptable loss of csPCa.</dc:description><dc:date>2022</dc:date><dc:source>http://zaguan.unizar.es/record/119842</dc:source><dc:doi>10.3390/cancers14205100</dc:doi><dc:identifier>http://zaguan.unizar.es/record/119842</dc:identifier><dc:identifier>oai:zaguan.unizar.es:119842</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/ISCIII/PI20/01666</dc:relation><dc:identifier.citation>Cancers 14, 20 (2022), 5100 [14 pp]</dc:identifier.citation><dc:rights>by</dc:rights><dc:rights>http://creativecommons.org/licenses/by/3.0/es/</dc:rights><dc:rights>info:eu-repo/semantics/openAccess</dc:rights></dc:dc>

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