首页> 外文期刊>Frontiers in Oncology >Diagnostic Accuracy of Droplet Digital PCR and Amplification Refractory Mutation System PCR for Detecting EGFR Mutation in Cell-Free DNA of Lung Cancer: A Meta-Analysis
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Diagnostic Accuracy of Droplet Digital PCR and Amplification Refractory Mutation System PCR for Detecting EGFR Mutation in Cell-Free DNA of Lung Cancer: A Meta-Analysis

机译:液滴数码PCR诊断准确性和扩增耐火突变体系PCR检测肺癌无细胞DNA中的EGFR突变:Meta分析

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Background: Epidermal growth factor receptor (EGFR) mutation testing in plasma cell-free DNA (cfDNA) from advanced lung cancer patients is an emerging clinical tool. This meta-analysis was designed to determine the diagnostic accuracy of two common PCR systems, droplet digital PCR (ddPCR) and amplification refractory mutation system PCR (ARMS-PCR), for detecting EGFR mutation in cfDNA. Materials and methods: A systematic search was carried out based on PubMed, Web of science, Embase and the Cochrane library. Data from eligible studies were extracted and pooled to calculate the sensitivity, specificity, diagnostic odds ratio (DOR), area under the summary receiver-operating characteristic curve (AUROC), using tissue biopsy results as the standard method. Subgroup analyses were performed regarding EGFR mutation type, tumor stage, and EGFR-TKI treatment. Results: Twenty-five studies involving 4,881 cases were included. The plasma testing sensitivity, specificity, DOR, and AUROC, compared with the matched tumor tissues, were 72.1%, 95.6%, 38.5, 0.89 for ddPCR, and 65.3%, 98.2%, 52.8, 0.71 for ARMS-PCR, respectively, through indirect comparison, significant differences were found in sensitivity ( P = 0.003) and specificity ( P = 0.007). Furthermore, significant difference was found in sensitivity between tumor stage subgroups (IIIB–IV subgroup vs. IA–IV subgroup) in ARMS-PCR (73.7 vs. 64.2%, P = 0.008), but not in ddPCR (72.5 vs. 71.2%, P = 0.756). Conclusions: This study demonstrates that ddPCR and ARMS-PCR have a high specificity with a practical sensitivity for detecting EGFR mutation in cfDNA, which supports their application as a supplement or a conditional-alternative to tissue biopsy in clinical practice for genotyping. It seems that ddPCR has a higher sensitivity than ARMS-PCR, especially in early stages.
机译:背景:来自晚期肺癌患者的血浆无细胞DNA(CFDNA)中的表皮生长因子受体(EGFR)突变试验是一种新兴的临床工具。该元分析旨在确定两个常见的PCR系统,液滴数字PCR(DDPCR)和扩增耐火突变体系PCR(ARMS-PCR)的诊断准确性,用于检测CFDNA中的EGFR突变。材料和方法:基于PubMed,Semase和Cochrane图书馆的PubMed。从符合条件的研究中提取和合并的数据以计算使用组织活组织检查结果作为标准方法的敏感性,特异性,诊断的曲线(DOR),区域,诊断率曲线(AUROC)。对EGFR突变型,肿瘤阶段和EGFR-TKI治疗进行亚组分析。结果:涉及4,881例案件的二十五项研究。与匹配的肿瘤组织相比,等离子体测试敏感性,特异性,DOR和Auroc分别为72.1%,95.6%,38.5,0.89,分别为65.3%,98.2%,52.8,0.71,通过间接比较,敏感性(P = 0.003)和特异性发现显着差异(P = 0.007)。此外,在肿瘤阶段亚组(IIIB-IV亚组与IA-IV亚组)之间的敏感性中发现了显着的差异(73.7与64.2%,P = 0.008),但不在DDPCR中(72.5 vs.71.2% ,p = 0.756)。结论:本研究表明,DDPCR和ARMS-PCR具有高特异性,具有高敏感性,用于检测CFDNA中的EGFR突变,其支持其作为补充剂或有条件替代的基因分型临床实践中的组织活组织检查。似乎DDPCR比Arms-PCR具有更高的敏感性,特别是在早期阶段。

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