Characterization of chronic graft-versus-host disease after haploidentical stem cell transplantation with posttransplant cyclophosphamide: a study on behalf of GETH-TC
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Fonseca Santos, Marta; Bailen, Rebeca; Lopez Godino, Oriana; Herruzo Delgado, Beatriz; Bermudez, Maria Aranzazu; García Cadenas, Irene; Huguet Mas, María; Ferra Coll, Christelle; Esquirol, Albert; Cortés Rodriguez, María; Yáñez San Segundo, Lucrecia
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2024Derechos
© 2024 The Author(s). Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (CCBY-NC-ND), where it is permissible to download and share the work provided it is properly cited.
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Transplantation, 2024, 108(10), 2134-2143
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Lippincott Williams & Wilkins
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Resumen/Abstract
Background. Chronic graft-versus-host disease (cGVHD) is a cause of late morbidity and nonrelapse mortality (NRM) after
allogenic hematopoietic stem cell transplantation (allo-HSCT). Although studies evaluating haploidentical allo-HSCT (haploHSCT) using posttransplant cyclophosphamide (PTCy) demonstrate lower cGVHD rates, comprehensive data describing the
clinical profile, risk factors, or outcomes of cGVHD within this platform are scarce. Methods. We conducted a retrospective
multicenter analysis of 389 consecutive patients who underwent haplo-HSCT PTCy in 7 transplant centers of the Spanish
Group Grupo Español de Trasplante Hematopoyético y Terapia Celular (GETH-TC) between 2008 and 2020 describing incidence, clinical profile, risk factors, and cGVHD outcomes. Results. Ninety-five patients of 389 developed cGVHD. Our data
revealed that the incidence and severity of cGVHD are lower than those reported for HLA-identical transplantation with conventional prophylaxis and that the strongest predictor for cGVHD was previous acute GVHD (P = 0.031). Also, recipient age
≥60 y (P = 0.044) was protective against cGVHD. Moreover, patients with moderate cGVHD had longer event-free survival at
3 y than other patients (P = 0.016) and a lower relapse rate at 3 y (P = 0.036). Conclusions. Our results support the fact
that the incidence and severity of cGVHD are lower than those reported for HLA-identical transplantation with conventional
prophylaxis. In this series, patients who develop moderate cGVHD after haplo-HSCT PTCy had a higher overall survival and
event-free survival, and lower relapse, suggesting higher graft-versus-leukemia effect. Although this is the largest series
focused on characterizing cGVHD in haplo-HSCT PTCy, further prospective studies are needed to confirm the findings.
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