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Título

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

AutorNovelli, Silvana; Bento, Leyre; García-Cadenas, Irene; Prieto, Laura CSIC ORCID ; López, Lucía; Gutiérrez, Gonzalo; Hernani, Rafael; Pérez, Ariadna; Esquirol, Albert; Solano, Carlos; Bastos-Oreiro, Mariana; Dorado, Nieves; Rodríguez, Nancy; Rodríguez-Real, Guillermo CSIC ORCID; Piñana, José Luis; Montoro, Juan; Herrera, Pilar; Luna, Alejandro; Parody, Rocío; Martín, Carmen CSIC ORCID; García, Estefanía; López, Oriana; Heras, Inmaculada; Zanabili, Joud; Moraleda, José María; Yáñez, Lucrecia; Gutiérrez, Antonio; Zudaire Ripa, Teresa; Córdoba, Raúl; Varela, Rosario; Ferrá, Christelle; Martínez, Joaquín; Martínez, Carmen; González-Barca, Eva; Martino, Rodrigo; Caballero, Dolores
Palabras claveAllogeneic stem cell transplantation
Haploidentical
T cell lymphoma
Fecha de publicaciónjun-2021
EditorElsevier
CitaciónTransplantation and Cellular Therapy 27(6): 493.e1-493.e8 (2021)
ResumenDespite 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 Español de Linfoma y Trasplante de Médula Ósea/Grupo Español de Trasplante Hematopoyético 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.
Versión del editorhttp://dx.doi.org/10.1016/j.jtct.2021.03.014
URIhttp://hdl.handle.net/10261/265350
DOI10.1016/j.jtct.2021.03.014
Identificadoresdoi: 10.1016/j.jtct.2021.03.014
issn: 2666-6367
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