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Mechanisms of resistance to BCR-ABL kinase inhibitors.

机译:对BCR-ABL激酶抑制剂的耐药机制。

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摘要

Since the introduction of imatinib mesylate (IM) for the treatment of chronic myeloid leukemia (CML), impressive clinical responses have been observed in the majority of patients in chronic phase. However, not all patients experience an optimal response to IM or even to the more potent, second-generation tyrosine kinase inhibitors (TKIs). Furthermore, responses are not sustained in a number of patients, and it is yet unclear whether the inhibitors can be safely discontinued in patients who achieve long-term remission. The emergence of resistance to TKIs has become a significant problem that has led to extensive studies on the causal mechanisms. This review describes our current state of knowledge on why and how CML cells can develop resistance to TKIs.
机译:自从将伊马替尼甲磺酸盐(IM)引入治疗慢性粒细胞白血病(CML)以来,大多数慢性期患者均获得了令人印象深刻的临床反应。但是,并非所有患者都能对IM甚至对更有效的第二代酪氨酸激酶抑制剂(TKI)产生最佳反应。此外,在许多患者中反应并未持续,并且尚不清楚在达到长期缓解的患者中是否可以安全地停用抑制剂。对TKI耐药性的出现已成为一个重要问题,已导致对其因果机制进行广泛研究。这篇评论描述了我们目前关于CML细胞为何以及如何产生对TKI耐药性的知识。

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