Please use this identifier to cite or link to this item: https://accedacris.ulpgc.es/jspui/handle/10553/142202
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dc.contributor.authorOrtiz López, Daviden_US
dc.contributor.authorMarchena Gómez, Joaquínen_US
dc.contributor.authorSosa Quesada, Yurenaen_US
dc.contributor.authorArtiles Armas, Manuelen_US
dc.contributor.authorArencibia Pérez, Beatrizen_US
dc.contributor.authorGil-García, Juliaen_US
dc.contributor.authorNogués-Ramía, Evaen_US
dc.contributor.authorRoque Castellano, Cristinaen_US
dc.date.accessioned2025-07-07T14:31:34Z-
dc.date.available2025-07-07T14:31:34Z-
dc.date.issued2025en_US
dc.identifier.issn2038-131Xen_US
dc.identifier.otherScopus-
dc.identifier.urihttps://accedacris.ulpgc.es/handle/10553/142202-
dc.description.abstractColorectal cancer (CRC) remains a major cause of cancer-related mortality despite advances in screening and treatment. Inflammation plays a key role in tumor progression, with the neutrophil-to-lymphocyte ratio (NLR) emerging as a potential prognostic marker. While preoperative NLR is a well-established predictor of survival, its prognostic value 1 year postoperatively remains underexplored. This study aims to evaluate the prognostic significance of NLR 1 year after curative CRC surgery, identify factors associated with its elevation, and assess its impact on survival and recurrence. A retrospective analysis was conducted on 788 patients who underwent curative-intent CRC surgery between 2015 and 2022. NLR was assessed preoperatively and 1 year postoperatively, using a cutoff of 3.3. Patients were categorized into four subgroups: “Low-Low”: NLR ≤ 3.3 pre- and postoperatively; “Low–High”: NLR ≤ 3.3 preoperatively but > 3.3 postoperatively; “High-Low”: NLR > 3.3 preoperatively but ≤ 3.3 postoperatively, and “High-High”: NLR > 3.3 at both time points. Survival analysis was performed using Cox regression. Postoperative NLR values were significantly lower than preoperative levels (median: 2.8 vs. 4.1, p < 0.001). An elevated post-NLR (> 3.3) correlated with poorer survival and higher recurrence rates. The “Low–High” group exhibited the worst prognosis, with a 5-year survival rate of 42.6% compared to 79.8% in the “Low-Low” group. Multivariate analysis confirmed post-NLR > 3.3 as an independent predictor of worse survival (HR: 3.49; 95%CI 2.41–5.04). Persistently elevated NLR 1 year after CRC surgery is associated with worse survival and higher recurrence. Routine postoperative NLR monitoring may help identify high-risk patients for closer follow-up and early intervention.en_US
dc.languageengen_US
dc.relation.ispartofUpdates in Surgeryen_US
dc.sourceUpdates in Surgery[ISSN 2038-131X], (Junio 2025)en_US
dc.subject32 Ciencias médicasen_US
dc.subject3213 Cirugíaen_US
dc.subject.otherColorectal Canceren_US
dc.subject.otherDisease-Free Survivalen_US
dc.subject.otherInflammatory Statusen_US
dc.subject.otherNeutrophil-To-Lymphocyte Ratioen_US
dc.subject.otherOverall Survivalen_US
dc.titlePrognostic impact of persistent postoperative neutrophil-to-lymphocyte ratio elevation 1 year after colorectal cancer surgeryen_US
dc.typeinfo:eu-repo/semantics/Articleen_US
dc.typeArticleen_US
dc.identifier.doi10.1007/s13304-025-02286-yen_US
dc.identifier.scopus105008901495-
dc.identifier.isi001517017900001-
dc.contributor.orcidNO DATA-
dc.contributor.orcid0000-0002-7362-1110-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.orcidNO DATA-
dc.contributor.authorscopusid57203399541-
dc.contributor.authorscopusid55089291600-
dc.contributor.authorscopusid57224572878-
dc.contributor.authorscopusid56667617500-
dc.contributor.authorscopusid55854192600-
dc.contributor.authorscopusid57194946042-
dc.contributor.authorscopusid57217064444-
dc.contributor.authorscopusid14032251400-
dc.identifier.eissn2038-3312-
dc.investigacionCiencias de la Saluden_US
dc.type2Artículoen_US
dc.contributor.daisngid10758675-
dc.contributor.daisngid594493-
dc.contributor.daisngid75656361-
dc.contributor.daisngid28898674-
dc.contributor.daisngid77608180-
dc.contributor.daisngid75660838-
dc.contributor.daisngid26358519-
dc.contributor.daisngid13782280-
dc.description.numberofpages12en_US
dc.utils.revisionen_US
dc.contributor.wosstandardWOS:Ortíz-López, D-
dc.contributor.wosstandardWOS:Marchena-Gómez, J-
dc.contributor.wosstandardWOS:Sosa-Quesada, Y-
dc.contributor.wosstandardWOS:Artiles-Armas, M-
dc.contributor.wosstandardWOS:Arencibia-Pérez, B-
dc.contributor.wosstandardWOS:Gil-García, J-
dc.contributor.wosstandardWOS:Nogués-Ramía, E-
dc.contributor.wosstandardWOS:Roque-Castellano, C-
dc.date.coverdateJunio 2025en_US
dc.identifier.ulpgcen_US
dc.contributor.buulpgcBU-MEDen_US
dc.description.sjr0,787
dc.description.jcr2,2
dc.description.sjrqQ1
dc.description.jcrqQ2
dc.description.scieSCIE
dc.description.miaricds11,0
item.grantfulltextopen-
item.fulltextCon 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.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.deptDepartamento de Ciencias Médicas y Quirúrgicas-
crisitem.author.orcid0000-0002-7362-1110-
crisitem.author.orcid0000-0002-7309-6141-
crisitem.author.parentorgIU de Investigaciones Biomédicas y Sanitarias-
crisitem.author.fullNameOrtiz López, David-
crisitem.author.fullNameMarchena Gómez, Joaquín-
crisitem.author.fullNameSosa Quesada, Yurena-
crisitem.author.fullNameArtiles Armas, Manuel-
crisitem.author.fullNameArencibia Pérez, Beatriz-
crisitem.author.fullNameRoque Castellano, Cristina-
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