egfr突变的非小细胞肺癌的免疫学特征和临床实践:一个叙述性的回顾。

IF 7.6 Q1 ONCOLOGY
Yi Dong , Liaqat Khan , Yi Yao
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引用次数: 0

摘要

免疫检查点抑制剂(ICIs)显著改善了晚期驱动阴性非小细胞肺癌(NSCLC)患者的预后。然而,靶向治疗仍然是晚期驱动阳性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的可变性,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)和其他免疫学特征,免疫治疗在该组中的应用仍是一个研究课题。因此,我们总结分析了NSCLC中不同EGFR突变的免疫学特征和调控机制,以及目前免疫治疗在EGFR突变人群中的临床应用情况,为今后的研究提供参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Immunological features of EGFR-mutant non-small cell lung cancer and clinical practice: a narrative review
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.
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