首页> 外文期刊>Blood: The Journal of the American Society of Hematology >Haploidentical, unmanipulated, G-CSF-primed bone marrow transplantation for patients with high-risk hematologic malignancies
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Haploidentical, unmanipulated, G-CSF-primed bone marrow transplantation for patients with high-risk hematologic malignancies

机译:高风险血液恶性肿瘤患者的单倍性,未操纵的G-CSF引发的骨髓移植

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摘要

Eighty patients with high-risk hematologic malignancies underwent unmanipulated, G-CSF-primed BM transplantation from an haploidentical family donor. Patients were transplanted in first or second complete remission (CR, standard-risk: n = 45) or in > second CR or active disease (high-risk: n = 35). The same regimen for GVHD prophylaxis was used in all cases. The cumulative incidence (CI) of neutrophil engraftment was 93% ± 0.1%. The 100-day CIs for II-IV and III-IV grade of acute GVHD were 24% ± 0.2% and 5% ± 0.6%, respectively. The 2-year CI of extensive chronic GVHD was 6% ± 0.1%. The 1-year CI of treatment-related mortality was 36% ± 0.3%. After a median follow-up of 18 months, 36 of 80 (45%) patients are alive in CR. The 3-year probability of overall and disease-free survival for standard-risk and high-risk patients was 54% ± 8% and 33% ± 9% and 44% ± 8% and 30% ± 9%, respectively. In multivariate analysis, disease-free survival was significantly better for patients who had standard-risk disease and received transplantations after 2007. We conclude that unmanipulated, G-CSF-primed BM transplantation from haploidentical family donor provides very encouraging results in terms of engraftment rate, incidence of GVHD and survival and represents a feasible, valid alternative for patients with high-risk malignant hematologic diseases, lacking an HLA identical sibling and in need to be urgently transplanted.
机译:80名高危血液恶性肿瘤患者接受了来自单倍体家庭供者的未经操纵的,G-CSF引发的BM移植。患者在第一次或第二次完全缓解(CR,标准风险:n = 45)或在第二次CR或活动性疾病(高风险:n = 35)中被移植。在所有情况下,均采用相同的GVHD预防方案。中性粒细胞植入的累积发生率(CI)为93%±0.1%。 II-IV级和III-IV级急性GVHD的100天CI分别为24%±0.2%和5%±0.6%。广泛的慢性GVHD的2年CI为6%±0.1%。与治疗相关的死亡率的1年CI为36%±0.3%。在中位随访18个月后,80例患者中有36例(45%)生存在CR中。标准风险和高风险患者的3年总体生存率和无疾病生存率分别为54%±8%和33%±9%和44%±8%和30%±9%。在多变量分析中,患有标准风险疾病并在2007年后接受移植的患者的无病生存期明显更好。我们得出的结论是,单倍体家庭供体的未经操纵的G-CSF初次BM移植在移植率方面提供了令人鼓舞的结果,GVHD的发生率和生存率,对于高危恶性血液病患者,缺乏HLA同胞且需要紧急移植的患者而言,是一种可行,有效的选择。

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