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一种FLT3酪氨酸激酶抑制剂对携带FLT3内部串联重复突变的急性髓系白血病母细胞具有选择性细胞毒性。

A FLT3 tyrosine kinase inhibitor is selectively cytotoxic to acute myeloid leukemia blasts harboring FLT3 internal tandem duplication mutations.

作者信息

Levis M, Tse K F, Smith B D, Garrett E, Small D

机构信息

Johns Hopkins University School of Medicine, Department of Oncology, Baltimore, MD 21231, USA.

出版信息

Blood. 2001 Aug 1;98(3):885-7. doi: 10.1182/blood.v98.3.885.

Abstract

Internal tandem duplication (ITD) mutations of the receptor tyrosine kinase FLT3 have been found in 20% to 30% of patients with acute myeloid leukemia (AML). These mutations constitutively activate the receptor and appear to be associated with a poor prognosis. Recent evidence that this constitutive activation is leukemogenic renders this receptor a potential target for specific therapy. In this study, dose-response cytotoxic assays were performed with AG1295, a tyrosine kinase inhibitor active against FLT3, on primary blasts from patients with AML. For each patient sample, the degree of cytotoxicity induced by AG1295 was compared to the response to cytosine arabinoside (Ara C) and correlated with the presence or absence of a FLT3/ITD mutation. AG1295 was specifically cytotoxic to AML blasts harboring FLT3/ITD mutations. The results suggest that these mutations contribute to the leukemic process and that the FLT3 receptor represents a therapeutic target in AML. (Blood. 2001;98:885-887)

摘要

在20%至30%的急性髓系白血病(AML)患者中发现了受体酪氨酸激酶FLT3的内部串联重复(ITD)突变。这些突变可组成性激活该受体,并且似乎与预后不良相关。近期有证据表明这种组成性激活具有致白血病作用,这使得该受体成为特异性治疗的潜在靶点。在本研究中,使用对FLT3有活性的酪氨酸激酶抑制剂AG1295对AML患者的原代母细胞进行了剂量反应细胞毒性试验。对于每个患者样本,将AG1295诱导的细胞毒性程度与对阿糖胞苷(Ara C)的反应进行比较,并与是否存在FLT3/ITD突变相关联。AG1295对携带FLT3/ITD突变的AML母细胞具有特异性细胞毒性。结果表明这些突变促成了白血病进程,并且FLT3受体是AML的一个治疗靶点。(《血液》。2001年;98:885 - 887)

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