精密医学
临床试验
肺癌
医学
靶向治疗
后天抵抗
个性化医疗
生物信息学
抗药性
药物开发
癌症
癌症研究
生物
药品
肿瘤科
内科学
药理学
病理
遗传学
作者
Marie‐Julie Nokin,Chiara Ambrogio,Ernest Nadal,David Santamarı́a
标识
DOI:10.1016/j.trecan.2020.11.005
摘要
The discovery of oncogenic driver mutations led to the development of targeted therapies with non-small cell lung cancer (NSCLC) being a paradigm for precision medicine in this setting. Nowadays, the number of clinical trials focusing on targeted therapies for uncommon drivers is growing exponentially, emphasizing the medical need for these patients. Unfortunately, similar to what is observed with most targeted therapies directed against a driver oncogene, the clinical response is almost always temporary and acquired resistance to these drugs invariably emerges. Here, we review the biology of infrequent genomic actionable alterations in NSCLC as well as the current and emerging therapeutic options for these patients. Mechanisms leading to acquired drug resistance and future challenges in the field are also discussed.
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