驱动基因阳性非小细胞肺癌的免疫治疗进展综述。

IF 3.5 2区 医学 Q2 ONCOLOGY
Translational lung cancer research Pub Date : 2025-07-31 Epub Date: 2025-07-28 DOI:10.21037/tlcr-2025-684
Fangfei Qian, Runbo Zhong, Hua Zhong
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引用次数: 0

摘要

背景与目的:尽管免疫疗法已成为驱动基因阴性的晚期非小细胞肺癌(NSCLC)的标准治疗方法,但其在驱动基因阳性的NSCLC患者中的疗效仍存在争议。本文系统地、批判性地分析了最近发表的文献,旨在改善驱动基因阳性非小细胞肺癌的免疫治疗现状。方法:检索PubMed、Web of Science、Scopus、谷歌Scholar等数据库中相关论文,包括在主要期刊和会议论文集上发表的相关文章。使用关键词(“免疫疗法”、“非小细胞肺癌”、“驱动基因阳性”)及其组合构建搜索查询。通过双重独立筛选和团队会议纳入文献,随后进行全面解读,形成一个高质量的文献语料库,重点关注驱动基因阳性NSCLC免疫治疗的进展。主要内容和发现:本文综述了驱动基因阳性NSCLC免疫治疗的最新进展和挑战,重点介绍了常见的驱动基因突变。不同驱动基因调节肿瘤免疫微环境的方式存在显著差异,导致不同的免疫治疗应答率。虽然靶向治疗是表皮生长因子受体(EGFR)突变的非小细胞肺癌的一线治疗,但当出现耐药性时,应探索免疫治疗联合治疗。免疫治疗加化疗是Kirsten大鼠肉瘤病毒癌基因同源(KRAS)突变的非小细胞肺癌患者的首选,而抗体-药物偶联加免疫治疗可能更适合人表皮生长因子受体2 (HER2)改变的非小细胞肺癌。尽管对常见病变患者的研究积累了很多,但对不常见病变患者的研究仍然缺乏。目前正在探索新辅助免疫治疗联合化疗治疗驱动基因阳性的非小细胞肺癌。结论:使用免疫疗法治疗驱动基因阳性的非小细胞肺癌仍存在许多问题。随着生物标志物和联合治疗的优化,个体化策略可能会进一步发展,以克服耐药性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Advances in immunotherapy for driver gene-positive non-small cell lung cancer: a narrative review.

Background and objective: Although immunotherapy has become the standard treatment for driver gene-negative advanced non-small cell lung cancer (NSCLC), its efficacy in driver gene-positive NSCLC patients remains conversational. This narrative review systematically and critically analyzes recently published literature, aiming to improve the current landscape of immunotherapy for driver gene-positive NSCLC.

Methods: The databases of PubMed, Web of Science, Scopus, and Google Scholar were searched for relevant articles, including those published in leading journals and conference proceedings. Search queries were constructed using keywords ("immunotherapy", "non-small cell lung cancer", "driver gene-positive") and their combinations. Literature was included via dual independent screening and team meetings, followed by comprehensive interpretation, resulting in a high-quality literature corpus focused on advances in immunotherapy for driver gene-positive NSCLC.

Key content and findings: This article reviews the recent advances and challenges in immunotherapy for driver gene-positive NSCLC, focusing on common driver gene mutations. Significant variations exist in how different driver genes regulate the tumor immune microenvironment, leading to disparate immunotherapy response rates. While targeted therapy is the first-line treatment for NSCLC with epidermal growth factor receptor (EGFR) mutations, immunotherapy combinations should be explored when drug resistance occurs. Immunotherapy plus chemotherapy is preferred in patients with Kirsten rat sarcoma viral oncogene homolog (KRAS)-mutated NSCLC, whereas antibody-drug conjugates plus immunotherapy may be more appropriate for NSCLC with human epidermal growth factor receptor 2 (HER2) alterations. Despite the accumulation of studies of patients with common alterations, studies of patients with uncommon alterations are still lacking. Neoadjuvant immunotherapy combined with chemotherapy is currently being explored for driver gene-positive NSCLC.

Conclusions: Many questions remain about the use of immunotherapy for the treatment of driver gene-positive NSCLC. With optimized biomarker and combination therapies, individualized strategies may be further developed for overcoming drug resistance.

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来源期刊
CiteScore
7.20
自引率
2.50%
发文量
137
期刊介绍: Translational Lung Cancer Research(TLCR, Transl Lung Cancer Res, Print ISSN 2218-6751; Online ISSN 2226-4477) is an international, peer-reviewed, open-access journal, which was founded in March 2012. TLCR is indexed by PubMed/PubMed Central and the Chemical Abstracts Service (CAS) Databases. It is published quarterly the first year, and published bimonthly since February 2013. It provides practical up-to-date information on prevention, early detection, diagnosis, and treatment of lung cancer. Specific areas of its interest include, but not limited to, multimodality therapy, markers, imaging, tumor biology, pathology, chemoprevention, and technical advances related to lung cancer.
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