克里唑蒂尼
间变性淋巴瘤激酶
碱性抑制剂
阿列克替尼
癌症研究
肺癌
酪氨酸激酶抑制剂
腺癌
突变
医学
生物
肿瘤科
内科学
癌症
基因
遗传学
恶性胸腔积液
作者
Gang Hua,Xing Zhang,Meiling Zhang,Qiang Wang,X. Chen,Ruoying Yu,Hua Bao,Jihu Liu,Xue Wu,Yang Shao,Bing Liang,Kaihua Lu
出处
期刊:ESMO open
[Elsevier]
日期:2022-02-01
卷期号:7 (1): 100337-100337
被引量:30
标识
DOI:10.1016/j.esmoop.2021.100337
摘要
Sequential postprogression plasma profiling revealed that increased lines of ALK inhibitors can accelerate the accumulation of ALK resistance mutations and may lead to treatment-refractory compound ALK mutations. The selection for optimal first-line TKI is very important to achieve a more efficacious long-term strategy and prevent the emergence of on-target resistance, which may provide guidance for clinical decision making.
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