医学
造血干细胞移植
骨髓衰竭
再生障碍性贫血
内科学
移植
骨髓移植
骨髓
疾病
儿科
造血
外科
胃肠病学
干细胞
遗传学
生物
作者
Carlo Dufour,Marta Pillon,Gèrard Socié,Alicia Rovó,Elisa Carraro,Andrea Bacigalupo,Rosi Oneto,Jakob Passweg,Antonio M. Risitano,André Tichelli,Régis Peffault de Latour,Hubert Schrezenmeier,Britta Hocshmann,Christina Peters,Austin Kulasekararaj,Anja van Biezen,Sujith Samarasinghe,Ayad Ahmed Hussein,Mouhab Ayas,Mahmoud Aljurf
摘要
This study analysed the outcome of 563 Aplastic Anaemia (AA) children aged 0-12 years reported to the Severe Aplastic Anaemia Working Party database of the European Society for Blood and Marrow Transplantation, according to treatment received. Overall survival (OS) after upfront human leucocyte antigen-matched family donor (MFD) haematopoietic stem cell transplantation (HSCT) or immunosuppressive treatment (IST) was 91% vs. 87% (P 0·18). Event-free survival (EFS) after upfront MFD HSCT or IST was 87% vs. 33% (P 0·001). Ninety-one of 167 patients (55%) failed front-line IST and underwent rescue HSCT. The OS of this rescue group was 83% compared with 91% for upfront MFD HSCT patients and 97% for those who did not fail IST up-front (P 0·017). Rejection was 2% for MFD HSCT and HSCT post-IST failure (P 0·73). Acute graft-versus-host disease (GVHD) grade II-IV was 8% in MFD graft vs. 25% for HSCT post-IST failure (P < 0·0001). Chronic GVHD was 6% in MFD HSCT vs. 20% in HSCT post-IST failure (P < 0·0001). MFD HSCT is an excellent therapy for children with AA. IST has a high failure rate, but remains a reasonable first-line choice if MFD HSCT is not available because high OS enables access to HSCT, which is a very good rescue option.
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