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dc.contributor.authorRuiz Díaz, Irune ORCID
dc.contributor.authorMartín Arruti, Maialen
dc.contributor.authorLópez López, Elixabet ORCID
dc.contributor.authorGarcía-Orad Carles, África ORCID
dc.date.accessioned2024-02-05T19:15:47Z
dc.date.available2024-02-05T19:15:47Z
dc.date.issued2014-05-09
dc.identifier.citationGynecologic Oncology 134(1) : 20-23 (2014)es_ES
dc.identifier.issn0090-8258
dc.identifier.urihttp://hdl.handle.net/10810/64671
dc.description.abstractObjective: Endometrial carcinomas of the endometrioid type (EEC) are associated with a good prognosis. However, about 20% of them recur and new prognostic markers are needed. Microsatellite instability (MSI), associated with mismatch repair (MMR) deficiency, is a frequent alteration in EECs that has been associated with prognosis. However, its prognostic impact on EECs remains unclear. The aim of the present study was to clarify the relationship between MMR deficiency and outcome in a large cohort of well classified EECs. Methods: A total of 212 EEC samples were analyzed by immunohistochemistry for the MMR genes MLH-1, MSH-2, MSH-6 and PMS-2. Kaplan-Meier survival analysis and log-rank tests were performed to study the prognostic significance of dMMR taking into account clinical and pathological parameters. Results: We observed no association between MMR deficiency and OS or PFS in our 212 EEC patients (p-value=0.6565 and 0.4380, respectively). When we performed the analysis in different FIGO-stage groups, we did not find association between MMR and OS or PFS in stages I, I/II or III/IV. When we analyzed the specific group of patients with lymphatic invasion separately, MMR expression was not associated with OS or PFS either. Conclusions: MMR deficiency does not seem to be a good prognostic marker in endometrioid type endometrial carcinomas.es_ES
dc.description.sponsorshipThis project was supported by the Spanish Network of Cooperative Investigation in Cancer RTICC (RD/06/0020/0048), Basque Government (IT661-13) and BIO Eusko Fundazioa BIOEF (BIO07/CA/021).es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/
dc.subjectmismatch repaires_ES
dc.subjectendometrioid carcinomas
dc.subjectimmunohistochemistry
dc.subjectoutcome
dc.titleLack of association between deficient mismatch repair expression and outcome in endometrial carcinomas of the endometrioid typees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2014 Elsevier Inc. under CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)es_ES
dc.relation.publisherversionhttps://doi.org/10.1016/j.ygyno.2014.04.053
dc.identifier.doi10.1016/j.ygyno.2014.04.053
dc.departamentoesGenética, antropología física y fisiología animales_ES
dc.departamentoeuGenetika,antropologia fisikoa eta animalien fisiologiaes_ES


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© 2014 Elsevier Inc. under CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)
Except where otherwise noted, this item's license is described as © 2014 Elsevier Inc. under CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/)