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首页> 外文期刊>Leukemia and lymphoma >Control of relapsed or refractory acute myeloid leukemia by clofarabine in preparation for allogeneic stem cell transplant
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Control of relapsed or refractory acute myeloid leukemia by clofarabine in preparation for allogeneic stem cell transplant

机译:氯法拉滨在准备异基因干细胞移植中控制复发性或难治性急性髓细胞性白血病

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摘要

Allogeneic stem cell transplant is indicated for patients with refractory or relapsed acute myeloid leukemia (AML). Since elimination of the leukemic load is thought to be a prerequisite for treatment success, we here investigate toxicity and anti-leukemic activity of a clofarabine-AraC salvage protocol preceding transplant. In this retrospective analysis, we observed induction of objective remissions in 86% of patients receiving clofarabine-AraC as compared to 83% with sequential high dose AraC/mitoxantrone (S-HAM) and 50% after mitoxantrone/topotecane/AraC (MTC) salvage strategies. In addition, clofarabine conferred anti-leukemic activity to some patients who failed initial MTC or S-HAM therapy. For overall and leukemia-free survival, we identified cytogenetically defined adverse risk markers but not response to therapy to be a strong predictor. In summary, the clofarabine-AraC salvage strategy combines pronounced anti-leukemic activity with an acceptable toxicity profile and allows the majority of patients with relapsed or refractory AML to proceed to allo-SCT, even in cytogenetically defined high risk situations.
机译:异基因干细胞移植适用于难治性或复发性急性髓细胞白血病(AML)患者。由于消除白血病负荷被认为是治疗成功的先决条件,因此我们在此研究了移植前使用氯法拉滨-AraC挽救方案的毒性和抗白血病活性。在这项回顾性分析中,我们观察到接受氯法拉滨-AraC的患者中有86%的患者获得了客观缓解,而连续高剂量AraC /米托蒽醌(S-HAM)的患者为83%,米托蒽醌/拓扑替康/ AraC(MTC)的挽救后为50%策略。此外,氯法拉滨还为一些最初的MTC或S-HAM治疗失败的患者提供了抗白血病活性。对于总体和无白血病生存,我们确定了细胞遗传学上定义的不良危险标志物,但对治疗的反应不是一个强有力的预测指标。总之,氯法拉滨-AraC的挽救策略将明显的抗白血病活性与可接受的毒性谱相结合,即使在细胞遗传学确定的高危情况下,也允许大多数复发或难治性AML患者进行异基因SCT。

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