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克服布鲁顿酪氨酸激酶抑制剂伊布替尼耐药突变的策略。

Strategies to overcome resistance mutations of Bruton's tyrosine kinase inhibitor ibrutinib.

机构信息

Jiangsu Key Laboratory of Drug Design & Optimization, China Pharmaceutical University, 24 Tongjiaxiang, Nanjing 210009, Peoples Republic of China.

Department of Medicinal Chemistry, School of Pharmacy, China Pharmaceutical University, 24 Tongjiaxiang, Nanjing 210009, Peoples Republic of China.

出版信息

Future Med Chem. 2018 Feb;10(3):343-356. doi: 10.4155/fmc-2017-0145. Epub 2018 Jan 19.

Abstract

Ibrutinib, as the first Bruton's tyrosine kinase (Btk) inhibitor, has been shown to have clinically significant activity in leukemias and lymphomas. However, the initially responsive tumors will develop resistance during the process of treatment in few patients. Here, we summarized the mechanism of acquired resistance and suggested the next-generation Btk inhibitors that override the target resistance. Moreover, the development of combination of selective antagonists or inhibitors targeting to multiple protein kinases have increased therapeutic potency to reduce the risk of the emergence of kinases inhibitor resistance. Thus, the reported combination of therapeutic drugs as an alternative therapy to overcome ibrutinib collapse or reduce the risk of the emergence of Btk inhibitor resistance also has been reviewed.

摘要

伊布替尼作为首个布鲁顿酪氨酸激酶(Btk)抑制剂,已在白血病和淋巴瘤中显示出具有临床意义的活性。然而,在少数患者的治疗过程中,最初有反应的肿瘤会产生耐药性。在这里,我们总结了获得性耐药的机制,并提出了克服靶耐药的新一代 Btk 抑制剂。此外,针对多种蛋白激酶的选择性拮抗剂或抑制剂的联合开发增加了治疗效力,以降低激酶抑制剂耐药性出现的风险。因此,还综述了报道的联合治疗药物作为替代疗法,以克服伊布替尼耐药或降低 Btk 抑制剂耐药性出现的风险。

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