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A phase I/II randomized trial of clofarabine or fludarabine added to idarubicin and cytarabine for adults with relapsed or refractory acute myeloid leukemia

机译:将氯氟沙比林或氟氯胺胺的一部分I / II随机试验添加到含紫芽蛋白和含有复发或难治性急性髓鞘白血病的成年人

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摘要

The purine nucleoside analogues clofarabine and fludarabine are active in acute myeloid leukemia (AML). We conducted a phase I/II randomized study of idarubicin and cytarabine with either clofarabine (CIA) or fludarabine (FIA) for relapsed or refractory AML. Clofarabine 15mg/m(2) was identified as the recommended phase II dose. Eighty-one patients were assigned using adaptive randomization to CIA (n=48) or FIA (n=33). The complete response (CR)/CR without platelet recovery rate did not differ between CIA and FIA (38% versus 30%, respectively; p=.50). In both arms, more than half of patients who had received only one prior line of therapy achieved remission. The median event-free survival for CIA and FIA was 2.0 and 1.9 months (p=.48), and the median overall survival was 6.3 and 4.7 months, respectively (p=.28). No significant differences in adverse events or early mortality rates were observed. Overall, CIA and FIA resulted in similar response rates and survival in patients with relapsed/refractory AML.
机译:嘌呤核苷类似物Clofarabine和Fludarabine在急性髓性白血病(AML)中是活性的。我们对含有氯苯胺(CIA)或Fludarabine(FIA)进行了一期I / II随机研究,用于复发或难治的AML。将15mg / m(2)鉴定为推荐的第二阶段剂量。使用适应性随机化对CIA(n = 48)或FIA(n = 33)分配八十一名患者。没有血小板回收率的完整反应(Cr)/ Cr在CIA和FIA之间没有区别(分别为38%,分别为30%; P = .50)。在双臂中,超过一半的患者只获得了一个先前的治疗方法取得了缓解。 CIA和FIA的中位活动存活率为2.0和1.9个月(P = .48),中位数分别为6.3和4.7个月(P = .28)。没有观察到不良事件或早期死亡率的显着差异。总体而言,CIA和FIA导致复发/难治性AML患者的反应率和生存率。

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