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dc.contributor.authorLópez Santillán, María
dc.contributor.authorLópez López, Elixabet ORCID
dc.contributor.authorÁlvarez González, Paula
dc.contributor.authorMartinez López, Garazi
dc.contributor.authorArzuaga Mendez, Javier
dc.contributor.authorRuiz Díaz, Irune ORCID
dc.contributor.authorGuerra Merino, Isabel
dc.contributor.authorGutiérrez Camino, Ángela ORCID
dc.contributor.authorMartín Guerrero, Idoia
dc.date.accessioned2021-10-04T11:24:13Z
dc.date.available2021-10-04T11:24:13Z
dc.date.issued2021-09
dc.identifier.citationCritical Reviews in Oncology Hematology 165 : (2021) // Article ID 103430es_ES
dc.identifier.issn1040-8428
dc.identifier.issn1879-0461
dc.identifier.urihttp://hdl.handle.net/10810/53215
dc.description.abstractDiffuse large B-cell lymphoma (DLBCL), the most common type of Non-Hodgkin lymphoma (NHL), is a highly heterogeneous and aggressive disease. Regardless of this heterogeneity, all patients receive the same first-line therapy, which fails in 30-40 % of patients, who are either refractory or relapse after remission. With the aim of stratifying patients to improve treatment outcome, different clinical and genetic biomarkers have been studied. The present systematic review aimed to identify somatic mutations that could serve as prognosis biomarkers or as therapeutic target mutations in DLBCL. Regarding their role as prognostic markers, mutations in CD58 and TP53 seem the most promising predictors of poor outcome although the combination of different alterations and other prognostic factors could be a more powerful strategy. On the other hand, different approaches regarding targeted therapy have been proposed. Therefore, mutational analysis could help guide treatment choice in DLBCL yet further studies and clinical trials are needed.es_ES
dc.description.sponsorshipThis study was funded by the Basque Government (IT989-16) and EiTB maratoia/Bioef (BIO15/CA/022/BC) . AGC was supported by a post-doctoral grant from the Basque Government.es_ES
dc.language.isoenges_ES
dc.publisherElsevieres_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectdiffuse large B-cell lymphomaes_ES
dc.subjectsomatic mutationes_ES
dc.subjectoutcomees_ES
dc.subjecthherapeutic targetes_ES
dc.subjectP53 gene-mutationspoor survivales_ES
dc.subjecttumor-suppressores_ES
dc.subjectrituximab-chopes_ES
dc.subjectTP53es_ES
dc.subjectpredictes_ES
dc.subjectEZH2es_ES
dc.subjectclassificationes_ES
dc.subjectmethylationes_ES
dc.subjectdisruptiones_ES
dc.titlePrognostic and therapeutic value of somatic mutations in diffuse large B-cell lymphoma: A systematic reviewes_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holderThis is an open access article distributed under the terms of the Creative Commons CC-BY license, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.es_ES
dc.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttps://www.sciencedirect.com/science/article/pii/S1040842821002183?via%3Dihubes_ES
dc.identifier.doi10.1016/j.critrevonc.2021.103430
dc.departamentoesGenética, antropología física y fisiología animales_ES
dc.departamentoeuGenetika,antropologia fisikoa eta animalien fisiologiaes_ES


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This is an open access article distributed under the terms of the Creative Commons CC-BY license, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Except where otherwise noted, this item's license is described as This is an open access article distributed under the terms of the Creative Commons CC-BY license, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.