冷冻保存细胞输注粒细胞集落刺激因子启动的供体淋巴细胞对造血细胞移植后晚期复发的急性白血病患者的益处

Sohn Sk
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摘要

异基因造血细胞移植(allo-HCT)后急性白血病复发尚无标准治疗方法。本研究评估了粒细胞集落刺激因子(G-CSF)-供体淋巴细胞输注(DLI)治疗急性白血病患者allo-HCT后复发的疗效。我们回顾性分析了255例接受异基因造血干细胞移植治疗急性白血病/骨髓增生异常综合征的患者。根据他们接受的CD34+细胞剂量将他们分为两组;CD34+较低组的患者接受的细胞数小于6×。在总生存率、无复发生存率和移植物抗宿主病(GVHD)无复发/无复发生存期方面,两组之间没有显著差异。在93名allo-HCT后复发的患者中,39名患者接受了G-CSF引发的DLI。根据复发的中位时间,这93名患者被分为早期或晚期复发组。在晚期复发组中,DLI组的一年总生存率显著高于非DLI组(53.4±7.4%vs 26.7±7.4%,p=0.039),而早期复发组没有差异。此外,DLI诱导的GVHD的发生率在两组之间没有差异。总之,在有限CD34+细胞剂量的allo-HCT后,用G-CSF引发的DLI治疗是一种可行且有效的选择,这可能会取代晚期复发患者的第二次HCT。
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Benefit of Granulocyte Colony-Stimulating Factor-Primed Donor Lymphocyte Infusion using Cryopreserved Cells for Patients with Acute Leukemia Who Relapsed Late after Hematopoietic Cell Transplantation
There is no standard therapy for relapse of acute leukemia after allogeneic Hematopoietic Cell Transplantation (allo-HCT). This study evaluated the efficacy of Granulocyte Colony-Stimulating Factor (G-CSF)-Primed Donor Lymphocyte Infusion (DLI) for patients with acute leukemia who relapsed after allo-HCT. We retrospectively reviewed 255 patients who received allo-HCT for acute leukemia/myelodysplastic syndrome. They were divided into two groups based on the CD34 + cell dose they received; patients in the lower CD34 + group received less than 6×10 6 cells/kg and those in the higher group received over 6×10 6 cells/kg. No significant differences were noted between the groups with respect to overall survival, relapse-free survival, and Graft- Versus -Host Disease (GVHD)-free/relapse-free survival. Among the 93 patients with relapse after allo-HCT, 39 patients received G-CSF-primed DLI. These 93 patients were classified into early or late relapse groups as defined by the median time to relapse. In the late relapse group, the one-year overall survival was significantly higher in the DLI group than in the non-DLI group (53.4±7.4% vs . 26.7±7.4%, p=0.039), whereas there were no differences in the early relapse group. In addition, the incidence of DLI-induced GVHD did not differ between the two groups. In conclusion, treatment with G-CSF-primed DLI after allo-HCT with a limited CD34 + cell dose is a feasible and effective option, which may replace a second HCT in late relapse patients.
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