间变性淋巴瘤激酶
ROS1型
碱性抑制剂
化学
癌症研究
激酶
肺癌
癌症
内科学
腺癌
生物化学
医学
恶性胸腔积液
作者
Sulman Basit,Zaman Ashraf,Kwangho Lee,Muhammad Latif
标识
DOI:10.1016/j.ejmech.2017.04.032
摘要
Non-small cell lung cancers (NSCLC) harboring anaplastic lymphoma kinase (ALK) gene rearrangements invariably develop resistance to 2nd-generation ALK inhibitors. Lorlatinib (PF-06463922) (6) is a 3rd-generation macrocyclic ALK-TKI that demonstrates many advantages over 2nd-generation ALK inhibitors. Lorlatinib has demonstrated decent kinase selectivity, promising pharmacokinetic profile, selective brain-penetration and strong antiproliferative activity in several ALK/ROS1-driven tumor models. The current review describes the activity spectrum, key events from discovery to clinical applications and the evidences that lorlatinib acts as an ALK/ROS1 inhibitor in clinical settings.
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