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在高危、复发或难治性急性髓系白血病和高级别骨髓增生异常综合征患者中,使用克拉屈滨/阿糖胞苷联合减低强度预处理和异基因造血干细胞移植进行细胞减灭治疗。

Cytoreductive treatment with clofarabine/ara-C combined with reduced-intensity conditioning and allogeneic stem cell transplantation in patients with high-risk, relapsed, or refractory acute myeloid leukemia and advanced myelodysplastic syndrome.

机构信息

Department of Hematology, Hemostasis, Oncology, and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.

出版信息

Eur J Haematol. 2012 Jan;88(1):52-60. doi: 10.1111/j.1600-0609.2011.01703.x. Epub 2011 Nov 17.

Abstract

The combination of cytoreductive chemotherapy with reduced-intensity conditioning (RIC) is a highly effective antileukemic therapy. Purpose of this retrospective analysis was to evaluate the antileukemic efficacy and toxicity of clofarabine-based chemotherapy followed by RIC and allogeneic stem cell transplantation (SCT) for high-risk, relapsed, or refractory acute myeloid leukemia (AML) or myelodysplastic syndromes (MDS). From May 2007 until October 2009, a total of 27 patients underwent allogeneic SCT after treatment with clofarabine and ara-C for 5d and RIC (4Gy TBI/cyclophosphamide/ATG). Prophylaxis of graft-versus-host disease (GvHD) consisted of cyclosporine and mycophenolate mofetil. Unmanipulated G-CSF mobilized PBSC (n=26) or bone marrow cells (n=1) were transplanted from unrelated (n=21) or matched related (n=6) donors. Non-hematological toxicities of this regimen mainly affected liver and skin and were all reversible. Seven patients relapsed within a median time of 5.7 months. The overall survival (OS) and relapse-free survival rates were 56% and 52% at 2 yr, respectively. In this cohort of patients, cytoreduction with clofarabine/ara-C (ClAraC) followed by RIC allogeneic SCT was well tolerated and showed good antileukemic efficacy even in patients with high-risk AML or MDS, with engraftment and GvHD-incidence comparable to other RIC regimens.

摘要

基于克拉屈滨的化疗联合低强度预处理(RIC)是一种高效的抗白血病疗法。本回顾性分析的目的是评估克拉屈滨联合阿糖胞苷化疗后行 RIC 及异基因造血干细胞移植(SCT)治疗高危、复发或难治性急性髓系白血病(AML)或骨髓增生异常综合征(MDS)的抗白血病疗效和毒性。2007 年 5 月至 2009 年 10 月,共 27 例患者接受克拉屈滨和阿糖胞苷治疗 5d 后,行 RIC(4GyTBI/环磷酰胺/ATG)及异基因 SCT。移植物抗宿主病(GVHD)预防方案为环孢素和霉酚酸酯。非清髓性 G-CSF 动员外周血造血干细胞(n=26)或骨髓细胞(n=1)均来自无关供者(n=21)或亲缘全相合供者(n=6)。该方案的非血液学毒性主要影响肝脏和皮肤,均为可逆性。7 例患者在中位时间 5.7 个月内复发。2 年时的总生存率(OS)和无复发生存率(RFS)分别为 56%和 52%。在该患者队列中,克拉屈滨/阿糖胞苷(ClAraC)联合 RIC 异基因 SCT 具有良好的耐受性,显示出良好的抗白血病疗效,即使在高危 AML 或 MDS 患者中,其植入和 GVHD 发生率与其他 RIC 方案相当。

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