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Pediatr Transplant ; 23(7): e13552, 2019 11.
Artículo en Inglés | MEDLINE | ID: mdl-31297928

RESUMEN

In this study, we report on major MRD or URD BMT outcomes in pediatric patients with SAA in Brazil. This was a retrospective study, which included 106 patients ≤18 years old who received a first BMT for SAA. All patients received bone marrow as graft source from an MRD (n = 69) or a URD (n = 37). Conditioning regimen was non-myeloablative in 73.6% of cases, and GVHD prophylaxis comprised a calcineurin inhibitor plus methotrexate in 89.6% of patients. After a median follow-up of 4.5 years after BMT, 81 patients are alive, with a 4-year OS of 77% and no statistically significant difference between the MRD and URD groups (82% vs. 69%, respectively; P = .08). Grade III-IV aGVHD at 6 months and cGVHD at 2 years were observed in 8% and 14% of cases, respectively, and were not statistically different between the groups. Twenty-five (23%) patients died at a median of 2.9 months after BMT. Our study showed that 4-year OS after BMT was not statistically different between MRD and URD recipients. This study shows that the outcomes of pediatric patients transplanted for SAA with a URD in Brazil are approaching those of MRD transplants. In contrast, OS after MRD BMT was lower than we would expect based on previous reports. The wide range of preparatory regimens used by the study centers highlights the need for standardized protocols for these children. Our findings provide a benchmark for future studies focused on improving BMT outcomes in this setting in Brazil.


Asunto(s)
Anemia Aplásica/terapia , Trasplante de Médula Ósea/métodos , Donante no Emparentado , Adolescente , Brasil , Niño , Preescolar , Países en Desarrollo , Femenino , Estudios de Seguimiento , Humanos , Lactante , Recién Nacido , Cooperación Internacional , Masculino , Estudios Retrospectivos , Índice de Severidad de la Enfermedad , Trasplante Homólogo , Resultado del Tratamiento , Washingtón
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