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成功进行非体外操作的单倍体相合造血干细胞移植并使用移植后环磷酰胺治疗一名患有唐氏综合征和骨髓增生异常综合征的儿童

Successful Unmanipulated Haploidentical Hematopoietic Stem Cell Transplant With Post-transplant Cyclophosphamide in a Child With Down Syndrome and Myelodysplastic Syndrome.

作者信息

Choed-Amphai Chane, Dror Yigal, Cada Michaela, Schechter Tal, Krueger Joerg, Ali Muhammad, Chopra Yogi

机构信息

Division of Hematology/Oncology, Department of Paediatrics, Blood and Marrow Transplant/Cellular Therapy Program, The Hospital for Sick Children.

Division of Pediatric Hematology and Oncology, Department of Pediatrics.

出版信息

J Pediatr Hematol Oncol. 2025 Jul 1;47(5):e199-e202. doi: 10.1097/MPH.0000000000003051. Epub 2025 May 12.

Abstract

Allogeneic hematopoietic stem cell transplant (HSCT) in children with Down syndrome and hematologic malignancies is challenging and is reserved for those who develop relapsed/refractory disease due to concerns regarding transplant-related mortality. Haploidentical HSCT, although performed in limited cases using graft manipulation methods to prevent graft-versus-host disease (GVHD), often results in dismal outcomes. Herein, we report a case of a 12-year-old boy with Down syndrome and myelodysplastic syndrome who underwent unmanipulated haploidentical HSCT using a reduced toxicity treosulfan-based conditioning and in vivo T-cell depletion with post-transplant cyclophosphamide. At the 1-year follow-up, he is alive with complete donor chimerism and no chronic GVHD.

摘要

对患有唐氏综合征和血液系统恶性肿瘤的儿童进行异基因造血干细胞移植(HSCT)具有挑战性,仅适用于那些因担心移植相关死亡率而出现复发/难治性疾病的患儿。单倍体相合造血干细胞移植虽然在少数病例中采用移植物处理方法来预防移植物抗宿主病(GVHD),但往往导致预后不佳。在此,我们报告一例12岁患有唐氏综合征和骨髓增生异常综合征的男孩,他接受了基于白消安的低毒性预处理方案以及移植后环磷酰胺体内T细胞清除的非处理单倍体相合造血干细胞移植。在1年的随访中,他存活且完全为供体嵌合体,无慢性移植物抗宿主病。

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