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在复发或难治性 AML 患者行异基因造血干细胞移植前采用氯法拉滨进行挽救治疗:BRIDGE 试验结果。

Clofarabine salvage therapy before allogeneic hematopoietic stem cell transplantation in patients with relapsed or refractory AML: results of the BRIDGE trial.

机构信息

Medizinische Klinik und Poliklinik I, Universitätsklinikum Carl Gustav Carus Dresden, Dresden, Germany.

Medizinische Klinik III, Klinikum Chemnitz, Chemnitz, Germany.

出版信息

Leukemia. 2016 Feb;30(2):261-7. doi: 10.1038/leu.2015.226. Epub 2015 Aug 18.


DOI:10.1038/leu.2015.226
PMID:26283567
Abstract

In patients with relapsed or refractory (r/r) acute myeloid leukemia (AML), long-term disease control can only be achieved by allogeneic hematopoietic stem cell transplantation (HSCT). We studied the safety and efficacy of clofarabine-based salvage therapy. The study was designed as phase II, multicenter, intent-to-transplant (ITT) study. A total of 84 patients with r/r AML were enrolled. All patients received at least one cycle of CLARA (clofarabine 30 mg/m(2) and cytarabine 1 g/m(2), days 1-5). Chemo-responsive patients with a donor received HSCT in aplasia after first CLARA. Generally, HSCT was performed as soon as possible. The conditioning regimen consisted of clofarabine (4 × 30 mg/m(2)) and melphalan (140 mg/m(2)). The median patient age was 61 years (range 40-75). On day 15 after start of CLARA, 26% of patients were in a morphologically leukemia-free state and 79% exposed a reduction in bone marrow blasts. Overall, 67% of the patients received HSCT within the trial. The primary end point, defined as complete remission after HSCT, was achieved by 60% of the patients. According to the ITT, overall survival at 2 years was 43% (95% confidence interval (CI), 32-54%). The 2-year disease-free survival for transplanted patients was 52% (95% CI, 40-69%). Clofarabine-based salvage therapy combined with allogeneic HSCT in aplasia shows promising results in patients with r/r AML.

摘要

在复发或难治性(r/r)急性髓系白血病(AML)患者中,异体造血干细胞移植(HSCT)是长期疾病控制的唯一方法。我们研究了基于氯法拉滨的挽救治疗的安全性和有效性。该研究设计为 II 期、多中心、意向移植(ITT)研究。共纳入 84 例 r/r AML 患者。所有患者均接受至少一个周期的 CLARA(氯法拉滨 30mg/m²和阿糖胞苷 1g/m²,第 1-5 天)治疗。对有供体的化疗反应患者在首次 CLARA 后出现造血功能衰竭时接受 HSCT。通常尽快进行 HSCT。预处理方案包括氯法拉滨(4×30mg/m²)和马法兰(140mg/m²)。中位患者年龄为 61 岁(范围 40-75 岁)。在 CLARA 开始后第 15 天,26%的患者达到形态学白血病无残留状态,79%的患者骨髓原始细胞减少。总体而言,67%的患者在试验中接受了 HSCT。主要终点定义为 HSCT 后的完全缓解,有 60%的患者达到该终点。根据 ITT,2 年总生存率为 43%(95%CI,32-54%)。移植患者的 2 年无病生存率为 52%(95%CI,40-69%)。基于氯法拉滨的挽救治疗联合造血功能衰竭时的异体 HSCT 在 r/r AML 患者中显示出良好的结果。

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