Please use this identifier to cite or link to this item: http://hdl.handle.net/2445/130889
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dc.contributor.authorMontalbo Calafell, Ruth-
dc.contributor.authorLozano Salvatella, Juan José-
dc.contributor.authorIzquierdo Reyes, Laura-
dc.contributor.authorIngelmo-Torres, Mercedes-
dc.contributor.authorBaños, Carmen-
dc.contributor.authorPalou, Joan-
dc.contributor.authorHeijden, Antoine G. van der-
dc.contributor.authorMedina, Rafael-
dc.contributor.authorSchmidbauer, Joerg-
dc.contributor.authorPrat Aparicio, Aleix-
dc.contributor.authorRibal, María José-
dc.contributor.authorAlcaraz Asensio, Antonio-
dc.contributor.authorMengual Brichs, Lourdes-
dc.date.accessioned2019-03-26T16:37:49Z-
dc.date.available2020-12-31T06:10:16Z-
dc.date.issued2019-02-07-
dc.identifier.issn1931-5244-
dc.identifier.urihttp://hdl.handle.net/2445/130889-
dc.description.abstractThis study aimed to improve our previous urine gene expression classifiers focusing on the detection of non-high-risk non-muscle-invasive bladder cancer (NMIBC), and develop a new classifier able to decrease the frequency of cystoscopies during bladder cancer (BC) patients' surveillance. A total of 597 urines from BC patients, controls and patients in follow-up for BC (PFBC) were included. The study has 3 phases. In the urinary biomarker discovery phase, 84 urines from BC and control patients were retrospectively included and analyzed by Ribonucleic Acid (RNA) sequencing. In the classifier development phase, a total of 132 selected genes from previous phase were evaluated by nCounter in 214 prospectively collected urines from PFBC (98 with tumor). A diagnostic classifier was generated by logistic regression. Finally, in the classifier validation phase, a multicentric and international cohort of 248 urines (134 BC and 114 nonrecurrent PFBC) was used to validate classifier performance. A total of 521 genes were found differentially expressed between non-high-risk NMIBC samples and all other groups (P < 0.05). An 8-gene diagnostic classifier with an area under curve (AUC) of 0.893 was developed. Validation of this classifier in a cohort of PFBC achieved an overall sensitivity (SN) and a negative predictive value (NPV) of 96% and 97%, respectively (AUC = 0.823). Notably, this accuracy was maintained in non-high-risk NMIBC group (SN = 94%; NPV = 98%). In conclusion, this 8-gene expression classifier has high SN and NPV in a real clinical scenario. The use of this classifier can reduce the number of follow-up cystoscopies in PFBC, although assessing its final place in clinical setting is necessary.-
dc.format.extent12 p.-
dc.format.mimetypeapplication/pdf-
dc.language.isoeng-
dc.publisherElsevier-
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1016/j.trsl.2019.02.003-
dc.relation.ispartofTranslational Research, The Journal of Laboratory and Clinical Medicine, 2019, vol. S1931-5244, num. 19, p. 30025-30028-
dc.relation.urihttps://doi.org/10.1016/j.trsl.2019.02.003-
dc.rightscc-by-nc-nd (c) Central Society for Clinical Research , 2019-
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/es-
dc.sourceArticles publicats en revistes (Cirurgia i Especialitats Medicoquirúrgiques)-
dc.subject.classificationDiagnòstic per la imatge-
dc.subject.classificationCàncer de bufeta-
dc.subject.classificationExpressió gènica-
dc.subject.otherDiagnostic imaging-
dc.subject.otherBladder cancer-
dc.subject.otherGene expression-
dc.titleAbility of a urine gene expression classifier to reduce the number of follow up cystoscopies in bladder cancer patients-
dc.typeinfo:eu-repo/semantics/article-
dc.typeinfo:eu-repo/semantics/acceptedVersion-
dc.identifier.idgrec686534-
dc.date.updated2019-03-26T16:37:49Z-
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess-
dc.identifier.pmid30771285-
Appears in Collections:Articles publicats en revistes (IDIBAPS: Institut d'investigacions Biomèdiques August Pi i Sunyer)
Articles publicats en revistes (Cirurgia i Especialitats Medicoquirúrgiques)

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