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阿糖胞苷与伊达比星联合应用的II期研究以及急性髓性白血病患者首次诱导疗程后持续存在原始细胞时人平衡核苷转运体1的表达情况。

A phase II study of elacytarabine in combination with idarubicin and of human equilibrative nucleoside transporter 1 expression in patients with acute myeloid leukemia and persistent blasts after the first induction course.

作者信息

Rizzieri David, Vey Norbert, Thomas Xavier, Huguet-Rigal Françoise, Schlenk Richard F, Krauter Jürgen, Kindler Thomas, Gjertsen Bjørn Tore, Blau Igor Wolfgang, Jacobsen Tove Flem, Johansen Malin, Bergeland Trygve, Gianella-Borradori Athos, Krug Utz

机构信息

Duke University Medical Center , Durham, NC , USA.

出版信息

Leuk Lymphoma. 2014 Sep;55(9):2114-9. doi: 10.3109/10428194.2013.867489. Epub 2014 Jan 24.

Abstract

Unlike cytarabine, cellular entry of Elacytarabine, the elaidic acid ester derivative of cytarabine, is independent of the human equilibrative nucleoside transporter 1 (hENT1). This phase II study tested whether the hENT1 blast expression level can be used as a predictive marker for cytarabine response and if the efficacy of elacytarabine is independent of hENT1 expression. A total of 51 patients with acute myeloid leukemia (AML) induction failure were given elacytarabine-idarubicin as a second induction course. The hENT1 expression level was analyzed prior to first induction and/or prior to treatment with elacytarabine. The overall response rate (ORR) was 41% and the safety profile was manageable. There is a trend suggesting that hENT1 expression influences response to cytarabine, but not sufficient to support it as a biomarker for guiding treatment. Further, we conclude that the activity of elacytarabine is not significantly predicted by the hENT1 expression level.

摘要

与阿糖胞苷不同,阿糖胞苷的反式油酸酯衍生物依拉阿糖胞苷进入细胞的过程不依赖于人平衡核苷转运体1(hENT1)。这项II期研究测试了hENT1原始细胞表达水平是否可作为阿糖胞苷反应的预测标志物,以及依拉阿糖胞苷的疗效是否独立于hENT1表达。共有51例急性髓系白血病(AML)诱导失败的患者接受依拉阿糖胞苷-伊达比星作为第二个诱导疗程。在首次诱导前和/或使用依拉阿糖胞苷治疗前分析hENT1表达水平。总缓解率(ORR)为41%,安全性可控。有趋势表明hENT1表达会影响对阿糖胞苷的反应,但不足以支持将其作为指导治疗的生物标志物。此外,我们得出结论,hENT1表达水平不能显著预测依拉阿糖胞苷的活性。

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