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Use of mitochondrial activity inhibitors for the treatment of acute myeloid leukemia with poor prognosis

机译:线粒体活性抑制剂在治疗预后较差的急性髓性白血病中的应用

摘要

Administering an effective amount of a mitochondrial activity inhibitor such as a Class A electron transport chain (ETC) complex I inhibitor, such as miglitinib or a pharmaceutically acceptable salt thereof, to a subject in need thereof to treat acute myelogenous A method for treating leukemia (AML) is disclosed. AML to be treated may be characterized by certain characteristics such as high levels of expression of one or more homeobox (HOX) -network genes, high and / or low expression of a particular gene, one or more cytogenetic or molecular risk factors, ( NK ), mutated NPM1 , mutated CEBPA , mutated FLT3 , mutated DNMT3A , mutated TET2 , mutated IDH1 , mutated IDH2 , mutated RUNX1 , mutated WT1 , mutated SRSF2 , abnormal karyotypes Characterized by the presence of a high frequency of intermediate cytogenetic hazards with interferon (abnK), trichomonic 8 (+8) and / or abnormal chromosome 5/7, and / or leukemia stem cells (LSC) .
机译:将有效量的线粒体活性抑制剂(例如A类电子传输链(ETC)复合物I抑制剂,例如米格利替尼或其药学上可接受的盐)给予需要此治疗的受试者,以治疗急性骨髓性白血病。 AML)。待治疗的AML可以通过某些特征来表征,例如一种或多种同源盒(HOX)网络基因的高水平表达,特定基因的高和/或低表达,一种或多种细胞遗传或分子危险因素( I> NK ),变异的 NPM1 ,变异的 CEBPA ,变异的 FLT3 ,变异的 DNMT3A ,变异的 TET2 ,已变异的 IDH1 ,已变异的 IDH2 ,已变异的 RUNX1 ,已变异的 WT1 ,已变异的 SRSF2 ,异常核型,其特征是干扰素(abnK),毛滴虫8(+8)和/或异常5/7染色体和/或白血病干细胞频繁出现中间细胞遗传学危害(LSC)。

著录项

  • 公开/公告号KR20190039730A

    专利类型

  • 公开/公告日2019-04-15

    原文格式PDF

  • 申请/专利权人 유니버시떼 드 몬트리얼;

    申请/专利号KR1020197005679

  • 发明设计人 소바고 기;바셀리 아이린;

    申请日2017-08-01

  • 分类号A61K31/4192;A61P35/02;C12Q1/6886;

  • 国家 KR

  • 入库时间 2022-08-21 11:51:08

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