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Allogeneic Stem Cell Transplantation in Mature T Cell and Natural Killer/T Neoplasias: A Registry Study from Spanish GETH/GELTAMO Centers

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dc.contributor.author Novelli,Silvana
dc.contributor.author Bento,Leyre
dc.contributor.author Garcia,Irene
dc.contributor.author Prieto,Laura
dc.contributor.author Lopez,Lucia
dc.contributor.author Gutierrez,Gonzalo
dc.contributor.author Hernani,Rafael
dc.contributor.author Perez,Ariadna
dc.contributor.author Esquirol,Albert
dc.contributor.author Solano,Carlos
dc.contributor.author Bastos,Mariana
dc.contributor.author Dorado,Nieves
dc.contributor.author Rodriguez,Nancy
dc.contributor.author Rodriguez,Guillermo
dc.contributor.author Pinana,Jose-L
dc.contributor.author Montoro,Juan
dc.contributor.author Herr
dc.date.accessioned 2025-10-20T14:40:34Z
dc.date.available 2025-10-20T14:40:34Z
dc.date.issued 2021-06
dc.identifier.citation Novelli S, Bento L, Garcia I, Prieto L, López L, Gutierrez G, et al. Allogeneic Stem Cell Transplantation in Mature T Cell and Natural Killer/T Neoplasias: A Registry Study from Spanish GETH/GELTAMO Centers. Transplantation and Cellular Therapy. junio de
dc.identifier.issn 2666-6375
dc.identifier.uri https://sms.carm.es/ricsmur/handle/123456789/20501
dc.description.abstract Despite advances in understanding the biology of mature T and natural killer (NK)/T cell neoplasia, current therapies, even the most innovative ones, are still far from ensuring its cure. The only treatment to date that has been shown to control aggressive T cell neoplasms in the long term is allogeneic stem cell transplantation (alloSCT). We aim to report the results of alloSCT for advanced mature T and NK/T neoplasias performed in centers from our national GELTAMO/GETH (Grupo Espanol de Linfoma y Trasplante de Medula Osea/Grupo Espanol de Trasplante Hematopoyetico y Terapia Celular) over the past 25 years. As a secondary objective, we analyzed the results of alloSCT from haploidentical donors. We performed a retrospective analysis of all patients who received an alloSCT in Spanish centers (n = 201) from September 1995 to August 2018. The 2-year overall survival (OS) and disease-free survival (DFS) were 65.5% and 58.2%, respectively. The univariate for OS and DFS showed statistically different hazard ratios for conditioning intensity, response pre-alloSCT, comorbidity index, donor/receptor cytomegalovirus status and Eastern Cooperative Oncology Group (ECOG) pre-alloSCT, but only a better ECOG pre-alloSCT remained significant in the multivariate analysis. There was an increased incidence of relapse in those patients who did not develop chronic graft-versus-host disease (GVHD) and an increased risk of death in those developing moderate to severe acute GVHD. The 1-year nonrelapse mortality was 21.9% and was mainly due to GVHD (30%) and bacterial infections (17%). When comparing unrelated donors with haploidentical donors, we found similar results in terms of OS and DFS. There was, however, a reduction of acute GVHD in the haploidentical group (P = .04) and trend to a reduction of chronic GVHD. In conclusion, alloSCT is the only curative option for most aggressive T cell neoplasias. Haploidentical donors offer similar results to related donors in terms of survival with a reduction of acute GVHD. (C) 2021 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.
dc.language.iso eng
dc.publisher ELSEVIER SCIENCE INC
dc.rights Atribución-NoComercial-SinDerivadas 3.0 España
dc.rights.uri http://creativecommons.org/licenses/by-nc-nd/3.0/es/ *
dc.subject.mesh Hematopoietic Stem Cell Transplantation
dc.subject.mesh Humans
dc.subject.mesh Killer Cells, Natural
dc.subject.mesh Neoplasm Recurrence, Local
dc.subject.mesh Registries
dc.subject.mesh Retrospective Studies
dc.subject.mesh Transplantation Conditioning
dc.title Allogeneic Stem Cell Transplantation in Mature T Cell and Natural Killer/T Neoplasias: A Registry Study from Spanish GETH/GELTAMO Centers
dc.type info:eu-repo/semantics/article
dc.identifier.pmid 33857447
dc.relation.publisherversion https://dx.doi.org/10.1016/j.jtct.2021.03.014
dc.type.version info:eu-repo/semantics/publishedVersion
dc.identifier.doi 10.1016/j.jtct.2021.03.014
dc.journal.title Transplantation and Cellular Therapy
dc.identifier.essn 2666-6367


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