Department of Pediatrics, Washington University in St. Louis, St. Louis, MO.
Pediatr Blood Cancer. 2020 Jan;67(1):e28030. doi: 10.1002/pbc.28030. Epub 2019 Oct 10.
Chronic granulomatous disease (CGD) is an immune deficiency characterized by defective neutrophil function and increased risk of life-threatening infections. Allogeneic hematopoietic cell transplantation is curative for CGD, and conditioning regimen impacts transplant-related outcomes. We report a single-center prospective study (NCT01821781) of four patients with CGD transplanted using a reduced-intensity conditioning regimen (RIC) containing alemtuzumab, fludarabine, melphalan, and thiotepa. Patients had early immune reconstitution with low incidence of infections. Disease-free survival was 75% at a median of five years after transplant. This RIC regimen presents an alternative approach for transplant of patients with CGD who may not tolerate busulfan-based conditioning.
慢性肉芽肿病(CGD)是一种免疫缺陷病,其特征为中性粒细胞功能缺陷和致命性感染风险增加。同种异体造血细胞移植是 CGD 的根治方法,而预处理方案会影响移植相关结局。我们报告了一项单中心前瞻性研究(NCT01821781),该研究纳入了 4 例采用含阿仑单抗、氟达拉滨、马法兰和噻替哌的减低强度预处理方案(RIC)移植的 CGD 患者。患者早期免疫重建,感染发生率低。移植后中位 5 年时无病生存率为 75%。该 RIC 方案为不能耐受以白消安为基础的预处理的 CGD 患者的移植提供了一种替代方法。