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CD34+ 阳性造血干细胞移植联合清髓性预处理方案治疗晚期骨髓纤维化患者。

CD34+ -selected hematopoietic stem cell transplant conditioned with a myeloablative regimen in patients with advanced myelofibrosis.

机构信息

Hematopoietic Cellular Therapy Program, Department of Medicine, University of Chicago Medicine, Chicago, IL, USA.

Department of Internal Medicine, Seoul National University Bundang Hospital, Seoul National University College of Medicine, Seongnam, Korea.

出版信息

Bone Marrow Transplant. 2022 Jul;57(7):1101-1107. doi: 10.1038/s41409-022-01684-9. Epub 2022 Apr 28.

Abstract

Allogeneic hematopoietic stem cell transplantation (Allo-HCT) remains the only curative treatment for myelofibrosis (MF). Transplantation in patients with MF is mostly done using a reduced intensity conditioning regimen with calcineurin inhibitors for graft versus host disease (GVHD) prophylaxis. Here we sought to evaluate outcomes of patients who underwent an ex vivo CD34+ -selected allo-HCT using myeloablative conditioning (MAC). Twenty-seven patients were included in this retrospective analysis. All patients were conditioned with busulfan, melphalan and fludarabine and antithymocyte globulin to prevent graft rejection. G-CSF mobilized peripheral blood stem cell grafts were depleted of T-cells using immunomagnetic CD34+ selection by CliniMACS device. Median follow-up among survivors was 50.6 months. The estimated 3-year overall survival, relapse free survival and the combined endpoint of GVHD/relapse free survival were 88% (95% CI, 75-100%), 80% (95% CI, 66-98%) and 74% (95% CI, 59-93%), respectively. The cumulative incidence of grade II-IV acute GVHD at day 100 was 33.3% (95% CI 16.4-51.3%), and two patients suffered chronic GVHD. There were no cases of primary graft failure. However, delayed graft failure occurred in two patients. We conclude that CD34+ selected allo-HCT with a MAC resulted in high survival rates in this cohort of patients with MF.

摘要

异基因造血干细胞移植(Allo-HCT)仍然是治疗骨髓纤维化(MF)的唯一根治方法。MF 患者的移植大多采用降低强度的预处理方案,并使用钙调神经磷酸酶抑制剂预防移植物抗宿主病(GVHD)。在此,我们试图评估接受过使用清髓性预处理(MAC)的体外 CD34+选择的异基因 HCT 的患者的结果。本回顾性分析共纳入 27 例患者。所有患者均接受了白消安、美法仑和氟达拉滨以及抗胸腺细胞球蛋白预处理,以防止移植物排斥。G-CSF 动员的外周血造血干细胞移植使用 CliniMACS 设备上的免疫磁珠 CD34+选择来去除 T 细胞。幸存者的中位随访时间为 50.6 个月。估计的 3 年总生存率、无复发生存率和 GVHD/无复发生存率的联合终点分别为 88%(95%CI,75-100%)、80%(95%CI,66-98%)和 74%(95%CI,59-93%)。第 100 天的 II-IV 级急性 GVHD 的累积发生率为 33.3%(95%CI,16.4-51.3%),有 2 例患者发生慢性 GVHD。没有原发性移植物失败的病例。然而,有 2 例患者发生迟发性移植物失败。我们得出结论,在该 MF 患者队列中,使用 MAC 的 CD34+选择的 allo-HCT 可获得高生存率。

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