Результаты применения асциминиба, первого аллостерического ингибитора BCR::ABL1-тирозинкиназы, у больных хроническим миелолейкозом со множественной резистентностью к предшествующей терапии

Q4 Medicine
А. Г. Туркина, Елена Андреевна Кузьмина
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引用次数: 0

Abstract

Currently, there is a crucial need for new treatment approaches to overcome the resistance and intolerance of several tyrosine kinase inhibitor (TKI) therapy lines in chronic myeloid leukemia (CML) patients. Asciminib, the first in its class BCR::ABL1-tyrosine kinase inhibitor specifically targeting ABL myristoyl pocket (STAMP), demonstrated efficacy and safety in CML patients with prior TKI therapy failure, including the cases with pan-resistant T315I mutation in the chimeric BCR::ABL1 gene. The present review focuses on the asciminib mechanism of action, the results of both preclinical and clinical phase I and III studies. Due to the favorable cardiovascular toxicity profile of asciminib, the scope of its application can be extended to patients with cardiovascular co-morbidities. Asciminib is registered in the Russian Federation in January 2023, so treatment algorithms for CML patients with ineffectiveness or intolerance of prior therapy should be updated in line with this new option.
第一个异位异质抑制剂ascminib的结果:慢性粒细胞白血病患者ABL1-甲基苯丙胺
目前,迫切需要新的治疗方法来克服几种酪氨酸激酶抑制剂(TKI)治疗线在慢性髓性白血病(CML)患者中的耐药和不耐受。Asciminib是首个靶向ABL肉豆醇口袋(STAMP)的BCR::ABL1酪氨酸激酶抑制剂,在先前TKI治疗失败的CML患者(包括嵌合BCR::ABL1基因泛耐药T315I突变的病例)中显示出疗效和安全性。本文综述了阿西米尼的作用机制,临床前和临床I期和III期研究的结果。由于阿西米尼良好的心血管毒性,其应用范围可扩展到心血管合并症患者。阿西米尼于2023年1月在俄罗斯联邦注册,因此针对先前治疗无效或不耐受的CML患者的治疗算法应根据这一新选择进行更新。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
0.80
自引率
0.00%
发文量
20
审稿时长
12 weeks
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