克拉斯
医学
临床试验
突变
病毒癌基因
抗性突变
癌症
癌症研究
药品
肿瘤科
药理学
内科学
结直肠癌
遗传学
逆转录酶
基因
生物
核糖核酸
作者
Xinting Zheng,Jiamin Luo,Wei Liu,Charles R. Ashby,Zhe‐Sheng Chen,Lizhu Lin
出处
期刊:Drugs of Today
[Prous Science]
日期:2022-04-01
卷期号:58 (4): 175-185
被引量:10
标识
DOI:10.1358/dot.2022.58.4.3400573
摘要
Sotorasib, a direct inhibitor of the enzyme Kirsten rat sarcoma viral oncogene (KRAS) with the G12C mutation, was approved by the U.S. Food and Drug Administration (FDA), as a second-line treatment for locally advanced or metastatic non-small cell lung cancer (NSCLC) containing the KRAS G12C mutation, on the basis of results of a phase II clinical trial (Code- BreaK100). In this article, we review the mechanism of action of KRAS G12C inhibitors and the latest clinical trials with sotorasib to provide a comprehensive understanding of its efficacy and toxicity. We also review the mechanisms that produce resistance to the KRAS G12C inhibitors and the preclinical research related to combination treatments for KRAS G12C-mutated tumors. Currently, clinical data suggests that sotorasib monotherapy has significant efficacy in NSCLC patients with the KRAS G12C mutation and tolerable toxicity, and it could represent a novel targeted therapy. Additional research will be required to delineate the mechanisms of resistance to sotorasib and determine the efficacy and safety of combination therapy for the treatment of NSCLC containing the KRAS G12C mutation.
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