血浆外泌体DNA检测非小细胞肺癌(NSCLC) EGFR突变的研究进展

IF 0.7 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Advanced biomedical research Pub Date : 2025-04-30 eCollection Date: 2025-01-01 DOI:10.4103/abr.abr_640_24
Mohammad Mehdi Jahani, Parisa Mashayekhi, Mir Davood Omrani, Azita Azimi Meibodi
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引用次数: 0

摘要

本综述系统评价了利用血浆外泌体DNA检测非小细胞肺癌(NSCLC)中表皮生长因子受体(EGFR)突变的相关文献,分析了从综合文献检索(PubMed, Embase, Web of Science;2010 - 2024)。研究结果显示,在所有研究中,EGFR突变的患病率范围很广(10%-26.8%),大多数突变位于外显子19和21。对比分析强调了血浆外泌体DNA (exDNA)作为组织活检的非侵入性替代方法的潜力,尽管不同液体活检方法(包括循环肿瘤细胞和exDNA分析)的敏感性和特异性存在显著差异。这种异质性强调了标准化和进一步验证的必要性,以优化血浆exDNA在检测EGFR突变、监测治疗反应和识别非小细胞肺癌耐药机制方面的临床应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Review of Plasma Exosomal DNA for Detecting EGFR Mutations in Non-Small Cell Lung Cancer (NSCLC).

This review systematically evaluated the literature on detecting epidermal growth factor receptor (EGFR) mutations in non-small cell lung cancer (NSCLC) using plasma exosomal DNA by analyzing data from eight studies selected from a comprehensive literature search (PubMed, Embase, Web of Science; 2010-2024). The findings revealed a wide range of EGFR mutation prevalence (10%-26.8%) across studies, with most mutations located in exons 19 and 21. Comparative analysis highlighted the potential of plasma exosomal DNA (exDNA) as a non-invasive alternative to tissue biopsy, although significant heterogeneity in sensitivity and specificity was observed across liquid biopsy methods (including circulating tumor cells and exDNA analyses). This heterogeneity underscores the need for standardization and further validation to optimize the clinical utility of plasma exDNA in detecting EGFR mutations, monitoring treatment response, and identifying resistance mechanisms in NSCLC.

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