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dc.contributor.authorDa Fonseca, Leonardo G.
dc.contributor.authorHashizume, Pedro H.
dc.contributor.authorde Oliveira, Irai Santana
dc.contributor.authorIzquierdo Sánchez, Laura
dc.contributor.authorSaud, Lisa Rodrigues da Cunha
dc.contributor.authorXerfan, Mariana Pinheiro
dc.contributor.authorAlves, Venancio Avancini Ferreira
dc.contributor.authorde Mello, Evandro Sobroza
dc.contributor.authorHerman, Paulo
dc.contributor.authorBañales Asurmendi, Jesús María ORCID
dc.contributor.authorOliveira, Claudia P.
dc.contributor.authorCarrilho, Flair J.
dc.date.accessioned2022-08-10T08:50:58Z
dc.date.available2022-08-10T08:50:58Z
dc.date.issued2022
dc.identifier.citationCancers 14(14) : (2022) // Article ID 3483es_ES
dc.identifier.issn2072-6694
dc.identifier.urihttp://hdl.handle.net/10810/57285
dc.description.abstractIntroduction and objectives: The incidence of cholangiocarcinoma (CCA) has been increasing globally. Although a concomitant increase in the incidence of metabolic disorders might suggest a causal relationship, the data are scarce. We aimed to describe the prevalence of metabolic disorders in patients with CCA and report the clinical features and outcomes. Patients and Methods: Retrospective study including patients with CCA. Patients were divided into: (1) past history of diabetes or/and overweight/obesity (“metabolic disorder group”) and (2) without any of these features (“non-metabolic-disorder group”). A Cox regression model was used to determine the prognostic factors. Results: 122 patients were included. In total, 36 (29.5%) had overweight/obesity, 24 (19.7%) had diabetes, and 8 (6.6%) had both. A total of 29 (23.8%) patients had resectable disease and received upfront surgery. A total of 104 (85.2%) received chemotherapy for advanced/recurrent disease. The overall survival of the cohort was 14.3 months (95% CI: 10.1–17.3). ECOG-PS 0 (p < 0.0001), resectable disease (p = 0.018) and absence of vascular invasion (p = 0.048) were independently associated with better prognosis. The “metabolic disorder group” (n = 52) had a median survival of 15.5 months (95% CI 10.9–33.9) vs. 11.5 months (95% CI 8.4–16.5) in the “non-metabolic-disorder group” (n = 70) (HR: 1.10; 95% CI 0.62–1.94). Patients with resectable disease in the “metabolic group” had longer survival than patients in the “non-metabolic group” (43.4 months (95% CI 33.9-NR) vs. 21.8 months (95% CI 8.6–26.9); HR = 0.12, 95% CI 0.03–0.59). Conclusion: Metabolic disorders are frequent among CCA patients. Underlying metabolic comorbidities may be associated with prognosis in resectable CCA. There is a need to explore the mechanism that drives CCA carcinogenesis in a metabolic background.es_ES
dc.language.isoenges_ES
dc.publisherMDPIes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectliver canceres_ES
dc.subjectcholangiocarcinomaes_ES
dc.subjectmetabolic syndromees_ES
dc.subjectdiabeteses_ES
dc.subjectobesityes_ES
dc.titleAssociation between Metabolic Disorders and Cholangiocarcinoma: Impact of a Postulated Risk Factor with Rising Incidencees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.date.updated2022-07-25T16:33:26Z
dc.rights.holder© 2022 by the authors.Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/).es_ES
dc.relation.publisherversionhttps://www.mdpi.com/2072-6694/14/14/3483es_ES
dc.identifier.doi10.3390/cancers14143483


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© 2022 by the authors.Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/).
Except where otherwise noted, this item's license is described as © 2022 by the authors.Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https:// creativecommons.org/licenses/by/ 4.0/).