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晚期非小细胞肺癌患者外周血循环肿瘤DNA中表皮生长因子受体突变的检测:一项遵循PRISMA标准的荟萃分析和系统评价

Detection of epidermal growth factor receptor mutations in peripheral blood circulating tumor DNA in patients with advanced non-small cell lung cancer: A PRISMA-compliant meta-analysis and systematic review.

作者信息

Zhou Shunkai, Huang Rongzhi, Cao Yunpeng

机构信息

Department of Thoracic Surgery, 900 Hospital of the Joint Logistics Team, Fuzhou.

Department of Cardiothoracic Surgery, Zhangzhou Affiliated Hospital of Fujian Medical University, Zhangzhou.

出版信息

Medicine (Baltimore). 2020 Oct 2;99(40):e21965. doi: 10.1097/MD.0000000000021965.

DOI:10.1097/MD.0000000000021965
PMID:33019389
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7535563/
Abstract

BACKGROUND

The epidermal growth factor receptor (EGFR) mutation status related to the treatment approach for advanced non-small cell lung cancer (NSCLC) patients. This study aimed to evaluate the diagnostic accuracy of peripheral blood circulating tumor DNA (ctDNA) in EGFR mutated advanced NSCLC patients.

METHOD

The related database was systematically searched with keywords until January 19, 2020. Studies contained the histopathological and cytological advanced NSCLC samples were included, and the diagnostic data were recorded for calculating sensitivity and specificity. I statistics were used for detecting heterogeneity across studies, and the meta-regression was performed to seek the source of heterogeneity.

RESULT

A total of 32 studies with 4527 advanced NSCLC patients were included in our meta-analysis. Among them, 87% of the patients were diagnosed as stage IV. The pooled sensitivity of peripheral blood ctDNA was 0.70 (95% CI: 0.63-0.75, I = 81.76) and the pooled specificity was 0.98 (95% CI: 0.96-0.99, I = 88.33). The meta-regression showed that the prospective study design and the ARMS detection method were the main source of heterogeneity for sensitivity (P < .05), and the publication country (Asia or non-Asia) was the main source of heterogeneity for specificity (P < .01).

CONCLUSION

ctDNA biopsy has high specificity and diagnostic accuracy in detection of EGFR mutation in advanced NSCLC patients. When the ctDNA gene test result is negative, we should fully consider the risk of missed diagnosis, and further tissue biopsy is still needed to undertake.

摘要

背景

表皮生长因子受体(EGFR)突变状态与晚期非小细胞肺癌(NSCLC)患者的治疗方法相关。本研究旨在评估外周血循环肿瘤DNA(ctDNA)在EGFR突变的晚期NSCLC患者中的诊断准确性。

方法

使用关键词系统检索相关数据库直至2020年1月19日。纳入包含组织病理学和细胞学晚期NSCLC样本的研究,并记录诊断数据以计算敏感性和特异性。采用I统计量检测各研究间的异质性,并进行Meta回归以寻找异质性来源。

结果

我们的Meta分析共纳入32项研究,涉及4527例晚期NSCLC患者。其中,87%的患者被诊断为IV期。外周血ctDNA的合并敏感性为0.70(95%CI:0.63-0.75,I = 81.76),合并特异性为0.98(95%CI:0.96-0.99,I = 88.33)。Meta回归显示,前瞻性研究设计和ARMS检测方法是敏感性异质性的主要来源(P < .05),发表国家(亚洲或非亚洲)是特异性异质性的主要来源(P < .01)。

结论

ctDNA活检在检测晚期NSCLC患者的EGFR突变方面具有较高的特异性和诊断准确性。当ctDNA基因检测结果为阴性时,应充分考虑漏诊风险,仍需进一步进行组织活检。

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