【单倍体造血干细胞移植治疗再生障碍性贫血11例造血重建不良患者供体纯化CD34(+)干细胞增强的临床分析】。

Q3 Medicine
Y He, Z L Xu, H Chen, Y Chen, T T Han, Y Y Zhang, M Lyu, X D Mo, C H Yan, Y Wang, Y Q Sun, X H Zhang, X J Huang, L P Xu
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引用次数: 0

摘要

目的:评价供体纯化CD34(+)干细胞增强治疗再生障碍性贫血(AA)患者单倍体造血干细胞移植(haploi - hsct)后造血重建不良(PHR)患者的安全性和有效性。方法:回顾性分析11例在北京大学人民医院行单倍造血干细胞移植并接受供体纯化CD34(+)干细胞增强治疗的AA和PHR患者。评估血细胞计数恢复、移植物抗宿主病(GVHD)发生率和总生存期(OS)。结果:11例PHR患者中,2例诊断为延长性孤立性血小板减少症(PT), 1例原发性移植物功能差(PGF), 8例诊断为继发性PGF。到PHR诊断的中位时间为110天(范围60-330天),从移植到纯化CD34(+)造血干细胞输注的中位时间间隔为194天(范围125-456天)。两例PT患者分别在CD34(+)干细胞输注后22天和13天实现血小板完全恢复。其余9例PGF患者中,6例造血功能完全恢复,中位绝对中性粒细胞计数恢复时间为19天(8-158天),HGB恢复时间为32.5天(13-158天),血小板恢复时间为31.5天(7-171天)。输注后慢性GVHD发生率为18.2%,未见急性GVHD病例。11例患者总生存率为90.9%(10/11),中位随访时间为614天(范围:153- 765天)。结论:供体纯化CD34(+)干细胞增强可能是单倍体造血干细胞移植后AA患者PHR的有效治疗策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Clinical analysis of donor-purified CD34(+) stem cell boost in 11 patients with poor hematopoietic reconstruction after haploid hematopoietic stem cell transplantation for aplastic anemia].

Objective: To evaluate the safety and efficacy of donor-purified CD34(+) stem cell boosts in patients with poor hematopoietic reconstruction (PHR) after haploid hematopoietic stem cell transplantation (haplo-HSCT) for aplastic anemia (AA) . Method: A retrospective analysis was conducted on 11 patients with AA and PHR who underwent haplo-HSCT and received donor-purified CD34(+) stem cell boosts at Peking University People's Hospital. Recovery of blood cell counts, incidence of graft-versus-host disease (GVHD), and overall survival (OS) were assessed. Results: Of the 11 patients with PHR, two were diagnosed with prolonged isolated thrombocytopenia (PT), one was primary poor graft function (PGF), and eight were diagnosed with secondary PGF. The median time to PHR diagnosis was 110 days (range: 60-330 days), and the median interval from transplantation to purified CD34(+) hematopoietic stem cell infusion was 194 days (range: 125-456 days). The two patients with PT achieved complete platelet recovery at 22 and 13 days after CD34(+) stem cell infusion, respectively. Among the remaining nine patients with PGF, six achieved complete hematopoietic recovery, with a median absolute neutrophil count recovery time of 19 days (8-158 days), HGB recovery time of 32.5 days (range: 13-158 days), and platelet recovery time of 31.5 days (range: 7-171 days). The incidence of chronic GVHD after infusion was 18.2%, with no cases of acute GVHD observed. The OS rate was 90.9% (10/11) in the 11 patients, with a median follow-up of 614 days (range: 153-1 765 days) . Conclusion: Donor-purified CD34(+) stem cell boost may be an effective therapeutic strategy for PHR in patients with AA after haplo-HSCT.

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