Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/167964
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dc.contributor.authorConnell, Shea P.-
dc.contributor.authorHanna, Marcel-
dc.contributor.authorMcCarthy, Frank-
dc.contributor.authorHurst, Rachel-
dc.contributor.authorWebb, Martyn-
dc.contributor.authorCurley, Helen-
dc.contributor.authorWalker, Helen-
dc.contributor.authorMills, Robert-
dc.contributor.authorBall, Richard Y.-
dc.contributor.authorSanda, Martin G.-
dc.contributor.authorPellegrini, Kathryn L.-
dc.contributor.authorPatil, Dattatraya-
dc.contributor.authorPerry, Antoinette S.-
dc.contributor.authorSchalken, Jack A.-
dc.contributor.authorPandha, Hardev-
dc.contributor.authorWhitaker, Hayley C.-
dc.contributor.authorDennis, Nening-
dc.contributor.authorStuttle, Christine-
dc.contributor.authorMills, Ian G.-
dc.contributor.authorGuldvik, Ingrid-
dc.contributor.authorMovember GAP1 Urine Biomarker Consortium-
dc.contributor.authorParker, Chris-
dc.contributor.authorBrewer, Daniel-
dc.contributor.authorCooper, Colin-
dc.contributor.authorClark, Jeremy-
dc.date.accessioned2020-07-07T11:51:00Z-
dc.date.available2020-07-07T11:51:00Z-
dc.date.issued2019-05-20-
dc.identifier.issn1464-4096-
dc.identifier.urihttp://hdl.handle.net/2445/167964-
dc.description.abstractObjectives: to develop a risk classifier using urine-derived extracellular vesicle RNA (UEV-RNA) capable of providing diagnostic information of disease status prior to biopsy, and prognostic information for men on active surveillance (AS). Patients and methods: post-digital rectal examination UEV-RNA expression profiles from urine (n = 535, multiple centres) were interrogated with a curated NanoString panel. A LASSO-based Continuation-Ratio model was built to generate four Prostate-Urine-Risk (PUR) signatures for predicting the probability of normal tissue (PUR-1), D'Amico Low-risk (PUR-2), Intermediate-risk (PUR-3), and High-risk (PUR-4) PCa. This model was applied to a test cohort (n = 177) for diagnostic evaluation, and to an AS sub-cohort (n = 87) for prognostic evaluation. Results: each PUR signature was significantly associated with its corresponding clinical category (p<0.001). PUR-4 status predicted the presence of clinically significant Intermediate or High-risk disease, AUC = 0.77 (95% CI: 0.70-0.84). Application of PUR provided a net benefit over current clinical practice. In an AS sub-cohort (n=87), groups defined by PUR status and proportion of PUR-4 had a significant association with time to progression (p<0.001; IQR HR = 2.86, 95% CI:1.83-4.47). PUR-4, when utilised continuously, dichotomised patient groups with differential progression rates of 10% and 60% five years post-urine collection (p<0.001, HR = 8.23, 95% CI:3.26-20.81). Conclusion: UEV-RNA can provide diagnostic information of aggressive PCa prior to biopsy, and prognostic information for men on AS. PUR represents a new & versatile biomarker that could result in substantial alterations to current treatment of PCa patients. This article is protected by copyright. All rights reserved.-
dc.format.extent12 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherWiley-
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1111/bju.14811-
dc.relation.ispartofBJU International, 2019, vol. 124, num. 4, p. 609-620-
dc.relation.urihttps://doi.org/10.1111/bju.14811-
dc.rights(c) BJU International, 2019-
dc.sourceArticles publicats en revistes (Patologia i Terapèutica Experimental)-
dc.subject.classificationIndicadors biològics-
dc.subject.classificationBiòpsia-
dc.subject.classificationCàncer de pròstata-
dc.subject.classificationOrina-
dc.subject.otherIndicators (Biology)-
dc.subject.otherBiopsy-
dc.subject.otherProstate cancer-
dc.subject.otherUrine-
dc.titleA four-group urine risk classifier for predicting outcome in prostate cancer patients-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec698883-
dc.date.updated2020-07-07T11:51:00Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid31106513-
Appears in Collections:Articles publicats en revistes (Patologia i Terapèutica Experimental)

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