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[表皮生长因子受体(EGFR)突变的晚期非小细胞肺癌免疫治疗进展]

[Progress of Immunotherapy in EGFR-mutated Advanced Non-small Cell Lung Cancer].

作者信息

Liu Yaoyao, Miao Jianlong

机构信息

Clinical Medical College of Jining Medical University, Jining 272000, China.

Pulmonary and Critical Care Medicine, Jining No. 1 People's Hospital, Jining 272000, China.

出版信息

Zhongguo Fei Ai Za Zhi. 2024 Jan 2;26(12):934-942. doi: 10.3779/j.issn.1009-3419.2023.106.26.

Abstract

Epidermal growth factor receptor-tyrosine kinase inhibitors (EGFR-TKIs) are currently the first-line standard of care for patients with non-small cell lung cancer (NSCLC) that harbor EGFR mutations. Nevertheless, resistance to EGFR-TKIs is inevitable. In recent years, although immune checkpoint inhibitors (ICIs) have significantly shifted the treatment paradigm in advanced NSCLC without driver mutation, clinical benefits of these agents are limited in patients with EGFR-mutated NSCLC. Compared with wild-type tumors, tumors with EGFR mutations show more heterogeneity in the expression level of programmed cell death ligand 1 (PD-L1), tumor mutational burden (TMB), and other tumor microenvironment (TME) characteristics. Whether ICIs are suitable for NSCLC patients with EGFR mutations is still worth exploring. In this review, we summarized the clinical data with regard to the efficacy of ICIs in patients with EGFR-mutated NSCLC and deciphered the unique TME in EGFR-mutated NSCLC.
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摘要

表皮生长因子受体酪氨酸激酶抑制剂(EGFR-TKIs)目前是携带EGFR突变的非小细胞肺癌(NSCLC)患者的一线标准治疗方案。然而,对EGFR-TKIs产生耐药是不可避免的。近年来,尽管免疫检查点抑制剂(ICIs)显著改变了无驱动基因突变的晚期NSCLC的治疗模式,但这些药物在EGFR突变的NSCLC患者中的临床获益有限。与野生型肿瘤相比,具有EGFR突变的肿瘤在程序性细胞死亡配体1(PD-L1)的表达水平、肿瘤突变负荷(TMB)和其他肿瘤微环境(TME)特征方面表现出更大的异质性。ICIs是否适用于EGFR突变的NSCLC患者仍值得探索。在这篇综述中,我们总结了关于ICIs在EGFR突变的NSCLC患者中的疗效的临床数据,并解读了EGFR突变的NSCLC中独特的TME。

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