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Título
Characterization of Chronic Graft-versus-host Disease After Haploidentical Stem Cell Transplantation With Posttransplant Cyclophosphamide: A Study on Behalf of GETH-TC
Autor(es)
Palabras clave
Stem cell
Fecha de publicación
2024
Editor
Lippincott, Williams & Wilkins
Citación
Fonseca-Santos, Marta MD1; Bailen, Rebeca MD, PhD2; Lopez-Godino, Oriana MD, PhD3; Herruzo-Delgado, Beatriz MD4; Bermudez, Maria Aranzazu MD, PhD5; García-Cadenas, Irene MD, PhD6; Huguet-Mas, María MD7; Ferra-Coll, Christelle MD, PhD7; Esquirol, Albert MD, PhD6; Cortés-Rodriguez, María1,8; Yañez-Sansegundo, Lucrecia MD, PhD5; Pascual-Cascon, Maria Jesus MD, PhD4; Heras, Inmaculada MD, PhD3; Kwon, Mi MD, PhD2; Lopez-Corral, Lucía MD, PhD1; on behalf of Grupo Español de Trasplante Hematopoyético y Terapia Celular. Characterization of Chronic Graft-versus-host Disease After Haploidentical Stem Cell Transplantation With Posttransplant Cyclophosphamide: A Study on Behalf of GETH-TC. Transplantation 108(10):p 2134-2143, October 2024. | DOI: 10.1097/TP.0000000000005034
Resumen
[EN]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 (haplo-HSCT) 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.
URI
ISSN
0041-1337
DOI
10.1097/TP.0000000000005034
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