Mehta Bhakti, Mahadeo Kris, Kapoor Neena, Abdel-Azim Hisham
Division of Hematology, Oncology, Blood and Marrow Transplantation, Children's Hospital Los Angeles, Los Angeles, CA, USA.
Pediatr Transplant. 2015 Jun;19(4):408-12. doi: 10.1111/petr.12471. Epub 2015 Apr 2.
HSCT with MAC is associated with durable donor engraftment for patients with CGD; however, MAC is limited by high rates of RRT. We used a novel RIC regimen with LD-TBI (200 cGy × two doses), fludarabine (30 mg/m(2) × three doses), and proximal alemtuzumab (0.5 mg/kg/dose × one dose) and unrelated donor grafts for consecutive patients with high-risk CGD who were not candidates for MAC at our institution. Among four children with CGD transplanted at our institution, three PBSC recipients are alive with sustained donor engraftment (median follow-up: two yr) and resolution of pre-HSCT active infections while one patient with bone marrow graft is alive after graft failure and autologous recovery. RIC may be a curative option for children with high-risk CGD.
对于慢性肉芽肿病(CGD)患者,采用大剂量化疗(MAC)的异基因造血干细胞移植(HSCT)与持久的供体植入相关;然而,MAC受到高比例肾脏替代治疗(RRT)的限制。我们对在本机构不符合MAC条件的连续高危CGD患者,使用了一种新型的减低预处理强度(RIC)方案,包括低剂量全身照射(LD-TBI,200 cGy×2次)、氟达拉滨(30 mg/m²×3次)和近端阿仑单抗(0.5 mg/kg/剂量×1次)以及无关供体移植物。在本机构接受移植的4例CGD患儿中,3例接受外周血干细胞移植的患者存活,供体持续植入(中位随访:2年),HSCT前的活动性感染得到缓解,而1例接受骨髓移植的患者在移植失败和自体恢复后存活。RIC可能是高危CGD患儿的一种治愈性选择。