Dong Yi, Khan Liaqat, Yao Yi
Cancer Center, Renmin Hospital of Wuhan University, Wuhan, China.
Research Center, Benazir Bhutto Hospital of Rawalpindi Medical University, Rawalpindi, Pakistan.
J Natl Cancer Cent. 2024 Jun 21;4(4):289-298. doi: 10.1016/j.jncc.2024.06.004. eCollection 2024 Dec.
Immune checkpoint inhibitors (ICIs) have significantly improved outcomes for patients with advanced driver-negative non-small cell lung cancer (NSCLC). However, targeted therapy remains the preferred treatment for advanced driver-positive NSCLC, including cases with epidermal growth factor receptor (EGFR) mutations. Considering the variability in EGFR-mutant NSCLC, including expression levels of programmed cell death ligand 1 (PD-L1), tumor mutation burden (TMB), and other immunological features, the application of immunotherapy in this group is still a subject of investigation. Therefore, we have summarized and analyzed the immunological characteristics and regulatory mechanisms of different EGFR mutations in NSCLC, as well as the current clinical application of immunotherapy in the EGFR-mutant population, to provide a reference for future research.
免疫检查点抑制剂(ICIs)显著改善了晚期驱动基因阴性非小细胞肺癌(NSCLC)患者的治疗效果。然而,靶向治疗仍然是晚期驱动基因阳性NSCLC的首选治疗方法,包括表皮生长因子受体(EGFR)突变的病例。考虑到EGFR突变型NSCLC的变异性,包括程序性细胞死亡配体1(PD-L1)的表达水平、肿瘤突变负荷(TMB)和其他免疫特征,免疫疗法在该组患者中的应用仍是一个研究课题。因此,我们总结并分析了NSCLC中不同EGFR突变的免疫特征和调节机制,以及免疫疗法在EGFR突变人群中的当前临床应用,以为未来的研究提供参考。