首页> 外文期刊>Blood: The Journal of the American Society of Hematology >The superiority of haploidentical related stem cell transplantation over chemotherapy alone as postremission treatment for patients with intermediate- or high-risk acute myeloid leukemia in first complete remission
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The superiority of haploidentical related stem cell transplantation over chemotherapy alone as postremission treatment for patients with intermediate- or high-risk acute myeloid leukemia in first complete remission

机译:单次相关干细胞移植优于单纯化疗作为初次完全缓解中,高危急性髓性白血病患者的缓解后治疗

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We report the results of a prospective, patient self-selected study evaluating whether haploidentical related donor stem cell transplantation (HRD-HSCT) is superior to chemotherapy alone as postremission treatment for patients with intermediate- or high-risk acute myeloid leukemia (AML) in first complete remission (CR1). Among totally 419 newly diagnosed AML patients, 132 patients with intermediate- and high-risk cytogenetics achieved CR1 and received chemotherapy alone (n = 74) or HSCT (n = 58) as postremission treatment. The cumulative incidence of relapse at 4 years was 37.5% ± 4.5%. Overall survival (OS) and disease-free survival (DFS) at 4 years were 64.5% ± 5.1% and 55.6% ± 5.0%, respectively. The cumulative incident of relapse for the HRD-HSCT group was significantly lower than that for the chemotherapy-alone group (12.0% ± 4.6% vs 57.8% ± 6.2%, respectively; P < .0001). HRD-HSCT resulted in superior survival compared with chemotherapy alone (4-year DFS, 73.1% ± 7.1% vs 44.2% ± 6.2%, respectively; P < .0001; 4-year OS, 77.5% ± 7.1% vs 54.7% ± 6.3%, respectively; P = .001). Multivariate analysis revealed postremission treatment (HRD-HSCT vs chemotherapy) and high WBC counts at diagnosis as independent risk factors affecting relapse, DFS, and OS. Our results suggest that HRD-HSCT is superior to chemotherapy alone as postremission treatment for AML.
机译:我们报告了一项前瞻性,患者自选研究的结果,该研究评估了单倍相关供体干细胞移植(HRD-HSCT)是否优于单纯化疗作为中度或高风险急性髓细胞性白血病(AML)患者缓解后的治疗方法首先完全缓解(CR1)。在总共419名新诊断的AML患者中,有132名中,高风险细胞遗传学患者获得了CR1,并且仅接受了化疗(n = 74)或HSCT(n = 58)作为缓解后治疗。 4年时复发的累积发生率为37.5%±4.5%。 4年时的总生存(OS)和无病生存(DFS)分别为64.5%±5.1%和55.6%±5.0%。 HRD-HSCT组的累积复发率显着低于单纯化疗组(分别为12.0%±4.6%和57.8%±6.2%; P <.0001)。与单独化疗相比,HRD-HSCT的生存率更高(分别为4年DFS,分别为73.1%±7.1%和44.2%±6.2%; P <.0001; 4年OS,分别为77.5%±7.1%和54.7%±分别为6.3%; P = 0.001)。多变量分析显示,缓解后治疗(HRD-HSCT与化学疗法相比)和高白细胞计数在诊断时是影响复发,DFS和OS的独立危险因素。我们的结果表明,HRD-HSCT作为AML的缓解后治疗优于单纯化疗。

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