Identificador persistente para citar o vincular este elemento: http://hdl.handle.net/10553/69900
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dc.contributor.authorHernández Hernández, Casandraen_US
dc.contributor.authorKim Lee, Daviden_US
dc.contributor.authorSánchez Pérez, Miriamen_US
dc.contributor.authorHernández Escobar, Sandraen_US
dc.date.accessioned2020-02-05T12:51:06Z-
dc.date.accessioned2020-09-28T09:33:48Z-
dc.date.available2020-02-05T12:51:06Z-
dc.date.available2020-09-28T09:33:48Z-
dc.date.issued2019en_US
dc.identifier.issn1558-7673en_US
dc.identifier.otherScopus-
dc.identifier.otherWoS-
dc.identifier.urihttp://hdl.handle.net/10553/69900-
dc.description.abstractThe Cancer of the Prostate Risk Assessment Postsurgical (CAPRA-S) score is a tool to stratify patients into groups according to their risk for biochemical recurrence after radical prostatectomy. Retrospective analysis was performed of data from 479 patients. The CAPRA-S score is a useful tool in patients to classify the risk of long-term biochemical progression of patients, thus helping decide if adjuvant treatment should be required.Background: The Cancer of the Prostate Risk Assessment Postsurgical (CAPRA-S) score is a tool to stratify patients into groups according to their risk for biochemical recurrence after radical prostatectomy. The aim of this study was to assess the accuracy of the CAPRA-S score for predicting biochemical progression at 5 and 10 years in our cohort of patients after radical prostatectomy. Patients and Methods: Between June 2004 and December 2015, radical prostatectomy was performed as the main treatment option for patients with localized prostate cancer. Patients who had received adjuvant or neoadjuvant treatment were excluded from this study. Biochemical progression after radical prostatectomy was considered in patients by prostate-specific antigen (PSA) > 0.1 ng/mL after surgery (biochemical persistence) and by at least 2 determinations of PSA > 0.2 ng/mL in those patients with initial undetectable postoperative PSA any time during their follow-up (biochemical failure). Cox proportional hazard model and Kaplan-Meier analysis were used for the statistical analysis. Results: Of 531 patients who underwent radical prostatectomy, 479 met the inclusion criteria. Mean follow-up was 85 months (min-max, 13-153 months). The rate of biochemical progression -free survival at 10 years was 84.2%, 55.1%, and 32.8%, respectively, for high-, intermediate-, and low-risk patients according to the CAPRA-S score. The concordance index for CAPRA-S predicting biochemical progression at 5 years was 0.71 and at 10 years was 0.70. Conclusion: The CAPRA-S score is a useful and easy-to-use tool in patients after radical prostatectomy to classify their risk for biochemical progression, thus helping decide if adjuvant treatment should be required.en_US
dc.languageengen_US
dc.relation.ispartofClinical Genitourinary Canceren_US
dc.sourceClinical Genitourinary Cancer [ISSN 1558-7673], v. 17 (3), p. e645-e649, (Junio 2019)en_US
dc.subject320713 Oncologíaen_US
dc.subject.otherDisease Progressionen_US
dc.subject.otherProstate Canceren_US
dc.subject.otherProstate Neoplasmsen_US
dc.subject.otherRecurrenceen_US
dc.subject.otherRisk Calculatoren_US
dc.titleAccuracy of CAPRA-S Score for Predicting Long-Term Biochemical Progression After Radical Prostatectomyen_US
dc.typeinfo:eu-repo/semantics/articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.clgc.2019.03.014en_US
dc.identifier.scopus85065426777-
dc.identifier.isi000470817300034-
dc.contributor.authorscopusid57193951964-
dc.contributor.authorscopusid57193951992-
dc.contributor.authorscopusid57193957475-
dc.contributor.authorscopusid57208647129-
dc.identifier.eissn1938-0682-
dc.description.lastpagee649en_US
dc.identifier.issue3-
dc.description.firstpagee645en_US
dc.relation.volume17en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.contributor.daisngid3877506-
dc.contributor.daisngid4040773-
dc.contributor.daisngid28349164-
dc.contributor.daisngid17935272-
dc.description.numberofpages5en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Hernandez, CH-
dc.contributor.wosstandardWOS:Lee, DK-
dc.contributor.wosstandardWOS:Perez, MS-
dc.contributor.wosstandardWOS:Escobar, SH-
dc.date.coverdateJunio 2019en_US
dc.identifier.ulpgces
dc.description.sjr0,97
dc.description.jcr2,695
dc.description.sjrqQ1
dc.description.jcrqQ2
dc.description.scieSCIE
item.grantfulltextnone-
item.fulltextSin texto completo-
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