Identificador persistente para citar o vincular este elemento: https://accedacris.ulpgc.es/handle/10553/145650
Campo DC Valoridioma
dc.contributor.authorAfonso-Luis, Nataliaen_US
dc.contributor.authorMonescillo-Martín, Ireneen_US
dc.contributor.authorMarchena Gómez, Joaquínen_US
dc.contributor.authorPlá Sánchez, Pauen_US
dc.contributor.authorCruz-Benavides, Franciscoen_US
dc.contributor.authorHernández Socorro, Carmen Rosaen_US
dc.date.accessioned2025-08-25T10:49:31Z-
dc.date.available2025-08-25T10:49:31Z-
dc.date.issued2025en_US
dc.identifier.issn2077-0383en_US
dc.identifier.otherScopus-
dc.identifier.urihttps://accedacris.ulpgc.es/handle/10553/145650-
dc.description.abstractBackground/Objectives: Inflammation-based markers have emerged as potential prognostic tools in hepatocellular carcinoma (HCC), but comparative data with classical prognostic factors in untreated HCC are limited. This study aimed to evaluate and compare the prognostic performance of inflammatory and conventional markers using Harrell’s concordance index (C-index). Methods: This retrospective study included 250 patients with untreated HCC. Prognostic variables included age, BCLC stage, Child–Pugh classification, Milan criteria, MELD score, AFP, albumin, Charlson comorbidity index, and the inflammation-based markers neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), monocyte-to-lymphocyte ratio (MLR), Systemic Inflammation Response Index (SIRI), and Systemic Immune-inflammation Index (SIII). Survival was analyzed using Cox regression. Predictive performance was assessed using the C-index, Akaike Information Criterion (AIC), and likelihood ratio tests. Results: Among the classical markers, BCLC showed the highest predictive performance (C-index: 0.717), while NLR ranked highest among the inflammatory markers (C-index: 0.640), above the MELD score and Milan criteria. In multivariate analysis, NLR ≥ 2.3 remained an independent predictor of overall survival (HR: 1.787; 95% CI: 1.264–2.527; p < 0.001), along with BCLC stage, albumin, Charlson index, and Milan criteria. Including NLR in the model modestly improved the C-index (from 0.781 to 0.794) but significantly improved model fit (Δ–2LL = 10.75; p = 0.001; lower AIC). Conclusions: NLR is an accessible, cost-effective, and independent prognostic marker for overall survival in untreated HCC. It shows discriminative power comparable to or greater than most conventional predictors and may complement classical stratification tools for HCC.en_US
dc.languageengen_US
dc.relation.ispartofJournal of Clinical Medicineen_US
dc.sourceJournal of Clinical Medicine [EISSN 2077-0383], v. 14 (15), p. 5514 (Agosto 2025)en_US
dc.subject32 Ciencias médicasen_US
dc.subject320101 Oncologíaen_US
dc.subject3205 Medicina internaen_US
dc.subject.otherHepatocarcinomaen_US
dc.subject.otherNeutrophil-To-Lymphocyte Ratioen_US
dc.subject.otherPrognostic Factorsen_US
dc.titleConcordance Index-Based Comparison of Inflammatory and Classical Prognostic Markers in Untreated Hepatocellular Carcinomaen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.3390/jcm14155514en_US
dc.identifier.scopus105013208687-
dc.identifier.isi001550714000001-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcid0000-0002-7362-1110-
dc.contributor.orcid0000-0002-3293-5068-
dc.contributor.orcidNO DATA-
dc.contributor.orcid0000-0001-8505-7740-
dc.contributor.authorscopusid57195537394-
dc.contributor.authorscopusid60042551900-
dc.contributor.authorscopusid55089291600-
dc.contributor.authorscopusid57204103461-
dc.contributor.authorscopusid6507852971-
dc.contributor.authorscopusid6505758785-
dc.identifier.eissn2077-0383-
dc.identifier.issue15-
dc.relation.volume14en_US
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.contributor.daisngidNo ID-
dc.description.numberofpages17en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Afonso-Luis, N-
dc.contributor.wosstandardWOS:Monescillo-Martín, I-
dc.contributor.wosstandardWOS:Marchena-Gómez, J-
dc.contributor.wosstandardWOS:Plá-Sánchez, P-
dc.contributor.wosstandardWOS:Cruz-Benavides, F-
dc.contributor.wosstandardWOS:Hernández-Socorro, CR-
dc.date.coverdateAgosto 2025en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr0,882
dc.description.jcr3,0
dc.description.sjrqQ1
dc.description.jcrqQ1
dc.description.scieSCIE
dc.description.miaricds10,5
item.grantfulltextnone-
item.fulltextSin texto completo-
crisitem.author.deptGIR IUIBS: Patología y Tecnología médica-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.deptGIR IUIBS: Grupo de investigaciones infecciosas, nutricionales e inflamatorias en pacientes hospitalarios-
crisitem.author.deptIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.deptDepartamento de Ciencias Clínicas-
crisitem.author.orcid0000-0002-7362-1110-
crisitem.author.orcid0000-0001-8505-7740-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameMarchena Gómez, Joaquín-
crisitem.author.fullNamePlá Sánchez, Pau-
crisitem.author.fullNameHernández Socorro, Carmen Rosa-
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