CAMS Key Laboratory of Translational Research on Lung Cancer, State Key Laboratory of Molecular Oncology, Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing 100021, China.
Int J Mol Sci. 2023 Sep 25;24(19):14521. doi: 10.3390/ijms241914521.
Outcome improvement in patients with driver-gene-negative advanced non-small cell lung cancer (NSCLC) has been significantly enhanced through targeting the immune system, specifically the PD-L1/PD-1 axis. Nevertheless, only a subset of patients with advanced NSCLC may derive benefits from immuno-monotherapy or immunotherapy combined with chemotherapy. Hence, in order to identify patients who will gain the maximum advantage from immunotherapy, it is crucial to investigate predictive biomarkers. This review provides a summary of the currently identified biomarkers associated with the extent of benefit from immuno-monotherapy or immunotherapy combined with chemotherapy in patients with advanced NSCLC. These biomarkers can be categorized into three groups: tumor-related, tumor-microenvironment-related, and host-factor-related.Tumor-related factors include PD-L1 expression, tumor mutational burden and specific genetic mutations, while tumor-microenvironment-related factors include extracellular vesicles and T-cell receptors, and host-related factors include systemic inflammation, circulating fatty acid profile, and the microbiome.
通过靶向免疫系统,特别是 PD-L1/PD-1 轴,驱动基因阴性的晚期非小细胞肺癌(NSCLC)患者的预后得到了显著改善。然而,只有一部分晚期 NSCLC 患者可能从免疫单药治疗或免疫联合化疗中获益。因此,为了确定哪些患者将从免疫治疗中获得最大益处,探索预测性生物标志物至关重要。本文综述了目前已确定的与晚期 NSCLC 患者免疫单药治疗或免疫联合化疗获益程度相关的生物标志物。这些生物标志物可分为三组:肿瘤相关、肿瘤微环境相关和宿主因素相关。肿瘤相关因素包括 PD-L1 表达、肿瘤突变负担和特定基因突变,而肿瘤微环境相关因素包括细胞外囊泡和 T 细胞受体,宿主相关因素包括全身炎症、循环脂肪酸谱和微生物组。