克拉斯
医学
肺癌
肿瘤科
内科学
突变体
癌症
结直肠癌
遗传学
生物
基因
作者
Enrica Capelletto,Paolo Bironzo,Louis J. Denis,Andrew Koustenis,Maristella Bungaro,Silvia Novello
出处
期刊:Future Oncology
[Future Medicine]
日期:2022-03-14
卷期号:18 (16): 1907-1915
被引量:15
标识
DOI:10.2217/fon-2021-1582
摘要
KRAS mutations occur in approximately 30% of lung adenocarcinomas, mainly in codon 12 (83% of cases), p.G12C being the prevalent one (40%), followed by p.G12V and p.G12D (22 and 16%, respectively). Treatment options for advanced KRAS mutant non-small-cell lung cancer (KRAS-MT NSCLC) are limited to chemotherapy and immune checkpoint inhibitors (CPIs). However, clinical trials exploring specific targeted agents are expected to change the treatment landscape of this disease. Here, we describe the design and scientific rationale of the randomized, phase II, open label, RAMP-202 study, which will evaluate the efficacy and safety of VS-6766 versus VS-6766 in combination with defactinib in advanced KRAS-MT NSCLC patients after failure of prior platinum-based chemotherapy and CPI.
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