阿替唑单抗
无容量
彭布罗利珠单抗
医学
免疫疗法
肿瘤科
生物标志物
内科学
PD-L1
精密医学
临床试验
个性化医疗
癌症
靶向治疗
肺癌
精确肿瘤学
重症监护医学
医学物理学
肿瘤微环境
癌症研究
癌症免疫疗法
病理
生物
生物化学
作者
Giovanni Rossi,Alessandro Russo,Marco Tagliamento,Alessandro Tuzi,Olga Nigro,Giacomo Vallome,Claudio Sini,Massimiliano Grassi,Maria Giovanna Dal Bello,Simona Coco,Luca Longo,Lodovica Zullo,Enrica T. Tanda,Chiara Dellepiane,Paolo Pronzato,Carlo Genova
出处
期刊:Cancers
[MDPI AG]
日期:2020-04-30
卷期号:12 (5): 1125-1125
被引量:42
标识
DOI:10.3390/cancers12051125
摘要
In recent years, the evolution of treatments has made it possible to significantly improve the outcomes of patients with non-small cell lung cancer (NSCLC). In particular, while molecular targeted therapies are effective in specific patient sub-groups, immune checkpoint inhibitors (ICIs) have greatly influenced the outcomes of a large proportion of NSCLC patients. While nivolumab activity was initially assessed irrespective of predictive biomarkers, subsequent pivotal studies involving other PD-1/PD-L1 inhibitors in pre-treated advanced NSCLC (atezolizumab within the OAK study and pembrolizumab in the Keynote 010 study) reported the first correlations between clinical outcomes and PD-L1 expression. However, PD-L1 could not be sufficient on its own to select patients who may benefit from immunotherapy. Many studies have tried to discover more precise markers that are derived from tumor tissue or from peripheral blood. This review aims to analyze any characteristics of the immunogram that could be used as a predictive biomarker for response to ICIs. Furthermore, we describe the most important genetic alteration that might predict the activity of immunotherapy.
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