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首页> 外文期刊>Experimental Hematology: Official Publication of the International Society for Experimental Hematology >BCR-ABL1 tyrosine kinase inhibitor K0706 exhibits preclinical activity in Philadelphia chromosome-positive leukemia
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BCR-ABL1 tyrosine kinase inhibitor K0706 exhibits preclinical activity in Philadelphia chromosome-positive leukemia

机译:BCR-ABL1酪氨酸激酶抑制剂K0706在费城染色体阳性白血病展示临床前活性

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摘要

BCR-ABL1 tyrosine kinase inhibitors (TKIs) are the cornerstone of treatment in chronic myeloid leukemia. Although there are now four TKIs approved for use in the front-line setting, acquired TKI resistance via secondary kinase domain mutations remains a problem for patients. K0706 is a novel BCR-ABL1 TKI currently under clinical investigation with structural elements similar to those of ponatinib and dasatinib. In this article, we functionally characterize the anti -leukemic activity of K0706 using cell proliferation assays in conjunction with drug resistance screening. We provide details from molecular modeling to support our in vitro findings and additionally describe our limited clinical experience with this drug in two patients treated on trial. We demonstrate that although K0706 retains efficacy against a large spectrum of clinically relevant mutations, it does not appear to have activity against BCR-ABL1(T3151). Early trial experience suggests excellent tolerability, which may positively affect the place of K0706 within the ever-expanding chronic myeloid leukemia treatment paradigm. (C) 2019 ISEH - Society for Hematology and Stem Cells. Published by Elsevier Inc. All rights reserved.
机译:BCR-ABL1酪氨酸激酶抑制剂(TKIS)是慢性骨髓白血病治疗的基石。虽然现在有四次TKIS用于前线设置,但通过次级激酶域突变获得的TKI电阻仍然是患者的问题。 K0706是目前在临床调查下的新型BCR-ABL1 TKI,其结构元素类似于Ponatinib和Dasatinib。在本文中,我们在用细胞增殖测定与药物阻塞筛选功能性地表征K0706的抗血肿活性。我们提供分子建模的细节,以支持我们的体外发现,另外描述我们在试验治疗的两名患者中对该药物的有限临床经验。我们证明,虽然K0706保持对临床相关突变的大谱的功效,但它似乎没有针对BCR-ABL1(T3151)的活性。早期试验体验表明,具有良好的耐受性,这可能会对慢性骨髓白血病治疗范例进行持续的K0706的位置。 (c)2019 ISEH - 血液学和干细胞社会。由elsevier Inc.保留所有权利发布。

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