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慢性髓性白血病中对酪氨酸激酶抑制剂耐药的当前研究进展

Current aspects in resistance against tyrosine kinase inhibitors in chronic myelogenous leukemia.

作者信息

Balabanov Stefan, Braig Melanie, Brümmendorf Tim H

出版信息

Drug Discov Today Technol. 2014 Mar;11:89-99. doi: 10.1016/j.ddtec.2014.03.003.

Abstract

Resistance against tyrosine kinase inhibitors (TKIs) represents a relevant clinical problem in treatment of chronic myelogenous leukemia (CML). On the basis of their activity against the spectrum of BCR-ABL mutations that have shown to be the most prominent mechanism of resistance to imatinib, new TKIs have been classified as second generation (such as nilotinib, dasatinib and bosutinib) or third generation (also cover- ing T315I such as ponatinib) TKIs. However, mutations in BCR-ABL only account for about half of the cases of treatment failure under TKI and other mechanisms either rendering the leukemic cells still dependent of BCR-ABL activity or supporting oncogenic properties of the leukemic cells independent of BCR-ABL signaling have been identified. A detailed understanding of the different underlying resistance mechanisms will be the prerequisite to eventually overcome clinical resistance and for the successful use of tailored combinations of targeted inhibitors in the future.

摘要

对酪氨酸激酶抑制剂(TKIs)产生耐药性是慢性髓性白血病(CML)治疗中一个重要的临床问题。基于其对已被证明是对伊马替尼耐药最主要机制的一系列BCR-ABL突变的活性,新的TKIs被分类为第二代(如尼罗替尼、达沙替尼和博舒替尼)或第三代(也包括针对T315I突变的如普纳替尼)TKIs。然而,BCR-ABL突变仅占TKI治疗失败病例的约一半,并且已经确定了其他机制,这些机制要么使白血病细胞仍然依赖BCR-ABL活性,要么支持白血病细胞不依赖BCR-ABL信号传导的致癌特性。深入了解不同的潜在耐药机制将是最终克服临床耐药性以及未来成功使用靶向抑制剂定制组合的先决条件。

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