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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/cancers14071828</dc:identifier><dc:language>eng</dc:language><dc:creator>Morote, Juan</dc:creator><dc:creator>Borque-Fernando, Angel</dc:creator><dc:creator>Triquell, Marina</dc:creator><dc:creator>Celma, Anna</dc:creator><dc:creator>Regis, Lucas</dc:creator><dc:creator>Mast, Richard</dc:creator><dc:creator>de Torres, Inés M.</dc:creator><dc:creator>Semidey, María E.</dc:creator><dc:creator>Santamaría, Anna</dc:creator><dc:creator>Planas, Jacques</dc:creator><dc:creator>Esteban, Luis M.</dc:creator><dc:creator>Trilla, Enrique</dc:creator><dc:title>Multiparametric Magnetic Resonance Imaging Grades the Aggressiveness of Prostate Cancer</dc:title><dc:identifier>ART-2022-128327</dc:identifier><dc:description>We sought to find further evidence showing the increase in PCa aggressiveness as PI-RADS score increases from four surrogates of PCa aggressiveness: i. prostate biopsy GG (≤3 vs. &amp;gt;3), ii. type of pathology in surgical specimens (favourable vs. unfavourable), iii. clinical stage (localised vs. advanced), and risk of recurrence of localised PCa after primary treatment (low-intermediate vs. high). A group of 692 PCa patients were diagnosed after 3-T multiparametric MRI (mpMRI) and guided and/or systematic biopsies, showing csPCa (GG ≥ 2) in 547 patients (79%) and insignificant PCa (iPCa) in 145 (21%). The csPCa rate increased from 32.4% in PI-RADS &amp;lt; 3 to 95.5% in PI-RADS 5 (p &amp;lt; 0.001). GG ≥ 3 was observed in 7.6% of PCa with PI-RADS &amp;lt; 3 and 32.6% in those with PI-RADS &amp;gt; 3 (p &amp;lt; 0.001). Unfavourable pathology was observed in 38.9% of PCa with PI-RAD &amp;lt; 3 and 68.3% in those with PI-RADS &amp;gt; 3 (p = 0.030). Advanced disease was not observed in PCa with PI-RADS ≤ 3, while it existed in 12.7% of those with PI-RADS &amp;gt; 3 (p &amp;lt; 0.001). High-risk recurrence localised PCa was observed in 9.5% of PCa with PI-RADS &amp;lt; 3 and 35% in those with PI-RADS &amp;gt; 3 (p = 0.001). The PI-RADS score was an independent predictor of all surrogates of PCa aggressiveness as PSA density. We confirmed that mpMRI grades PCa aggressiveness.</dc:description><dc:date>2022</dc:date><dc:source>http://zaguan.unizar.es/record/112188</dc:source><dc:doi>10.3390/cancers14071828</dc:doi><dc:identifier>http://zaguan.unizar.es/record/112188</dc:identifier><dc:identifier>oai:zaguan.unizar.es:112188</dc:identifier><dc:relation>info:eu-repo/grantAgreement/ES/ISCIII/PI20/01666</dc:relation><dc:identifier.citation>Cancers 14, 7 (2022), 1828 [9 p.]</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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