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dc.contributor.authorJiménez Vicente, Carlos
dc.contributor.authorEsteve, Jordi
dc.contributor.authorBaile González, Mónica
dc.contributor.authorPérez López, Estefanía
dc.contributor.authorMartin Calvo, Carmen
dc.contributor.authorAparicio, Clara
dc.contributor.authorOiartzabal Ormategi, Itziar
dc.contributor.authorEsquirol, Albert
dc.contributor.authorPeña Muñoz, Felipe
dc.contributor.authorFernández Luis, Sara
dc.contributor.authorHeras Fernando, Inmaculada
dc.contributor.authorGonzález Rodríguez, Ana Pilar
dc.contributor.authorLópez García, Alberto
dc.contributor.authorLópez Lorenzo, Jose Luis
dc.contributor.authorTorrado, Tamara
dc.contributor.authorSáez Marín, Adolfo Jesús
dc.contributor.authorAcosta Fleytas, Cynthia
dc.contributor.authorGarcía, Lucía
dc.contributor.authorVillar, Sara
dc.contributor.authorFilaferro, Silvia
dc.contributor.otherUniversidad de Cantabriaes_ES
dc.date.accessioned2025-07-09T11:11:24Z
dc.date.available2025-07-09T11:11:24Z
dc.date.issued2025
dc.identifier.issn2044-5385
dc.identifier.urihttps://hdl.handle.net/10902/36639
dc.description.abstractThis multicenter retrospective study by GETH-TC validates the prognostic value of the Allo-HCT Refined ELN 2022 risk classification in allografted AML patients. The new classification refines the ELN 2022 risk classification, dividing adverse-risk patients into two subgroups: Adv-Plus (AdvP), including those with complex karyotype, MECOM (EVI1) rearrangement, or TP53 mutations/del(17p), and an additional adverse group (Adv*). The study included 651 AML patients treated with at least one line of anthracycline-based induction therapy and in complete remission. According to the Allo-HCT Refined ELN 2022 risk classification, 19.4% (n = 126) patients were classified into the Favorable (Fav) risk, 38.1% (n = 248) into the Intermediate (Int) risk, 27.2% (n = 177) in the Adv* and 15.4% (n = 100) in the AdvP. Outcomes were significantly poorer for patients allocated in the AdvP risk group (5-year OS rate: 32.3%, 5-year LFS rate: 24.3%, both p < 0.001 with the rest of subgroups) and a higher CIR (5-year CIR: 64.3%, p < 0.001). Patients in the Adv* risk group had similar outcomes than patients in the Int risk group (5-year OS rate: 70.2% vs. 66.7%, p = 0.69, 5-year LFS rate: 63.8% vs. 55.9%, p = 0.33). Multivariate analysis confirmed the dismal outcomes for AdvP patients for OS: Hazard Ratio (HR) = 3.05, and LFS: HR = 2.66, both p < 0.001. Our findings validate the Allo-HCT Refined ELN 2022 classification as a robust prognostic tool, particularly highlighting the poor outcomes for the AdvP subgroup.es_ES
dc.description.sponsorshipWe thank our patients and the Grupo Español de Trasplante Hematopoyético y Terapia Celular (GETH-TC) for the support provided during the study development. In addition, Dr. Jordi Esteve and María Jesús Pascual Cascón for their mentorship and support during the study period. We additionally thank REDCap (Research Electronic Data Capture) service for permitting the use of their service without costs. REDCap is a secure, web-based software platform designed to support data capture for research studies.es_ES
dc.format.extent9 p.es_ES
dc.language.isoenges_ES
dc.publisherNature Pub. Groupes_ES
dc.rightsAttribution-NonCommercial NoDerivatives 4.0 International © The Authors 2025es_ES
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.sourceBlood Cancer Journal, 2025, 15(1), 42es_ES
dc.titleAllo-HCT refined ELN 2022 risk classification: validation of the Adverse-Plus risk group in AML patients undergoing allogeneic hematopoietic cell transplantation within the Spanish Group for Hematopoietic Cell Transplantation (GETH-TC)es_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.relation.publisherVersionhttps://doi.org/10.1038/s41408-025-01223-xes_ES
dc.rights.accessRightsopenAccesses_ES
dc.identifier.DOI10.1038/s41408-025-01223-x
dc.type.versionpublishedVersiones_ES


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Attribution-NonCommercial NoDerivatives 4.0 International © The Authors 2025Excepto si se señala otra cosa, la licencia del ítem se describe como Attribution-NonCommercial NoDerivatives 4.0 International © The Authors 2025