间变性淋巴瘤激酶
克里唑蒂尼
医学
癌症研究
肺癌
后天抵抗
突变
融合基因
酪氨酸激酶
碱性抑制剂
腺癌
基因
激酶
肿瘤科
癌症
内科学
生物
遗传学
受体
恶性胸腔积液
作者
Yue Pan,Yue Zeng,Yurong Peng,Xiaohan Liu,Yizheng Li,Fang Wu
标识
DOI:10.1016/j.ejca.2022.02.001
摘要
Anaplastic lymphoma kinase (ALK) tyrosine kinase inhibitors are the preferred initial treatment for ALK rearranged non-small cell lung cancer (NSCLC). While initial responses to next-generation inhibitors are robust, acquired resistance is expected for nearly all patients. The emergence of the G1202R mutation represents a significant concern for oncologists, as it predicts resistance to almost all ALK inhibitors (ALKi) other than lorlatinib. However, we report the first case of ALK de novo mutation in a patient with advanced NSCLC that responded to brigatinib.
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