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The Diagnostic Performance of Stool DNA Testing for Colorectal Cancer: A Systematic Review and Meta-Analysis

机译:粪便DNA检测对大肠癌的诊断性能:系统评价和Meta分析

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This meta-analysis was designed to evaluate the diagnostic performance of stool DNA testing for colorectal cancer (CRC) and compare the performance between single-gene and multiple-gene tests. MEDLINE, Cochrane, EMBASE databases were searched using keywords colorectal cancers, stool/fecal, sensitivity, specificity, DNA, and screening. Sensitivity analysis, quality assessments, and performance bias were performed for the included studies. Fifty-three studies were included in the analysis with a total sample size of 7524 patients. The studies were heterogeneous with regard to the genes being analyzed for fecal genetic biomarkers of CRC, as well as the laboratory methods being used for each assay. The sensitivity of the different assays ranged from 2% to 100% and the specificity ranged from 81% to 100%. The meta-analysis found that the pooled sensitivities for single- and multigene assays were 48.0% and 77.8%, respectively, while the pooled specificities were 97.0% and 92.7%. Receiver operator curves and diagnostic odds ratios showed no significant difference between both tests with regard to sensitivity or specificity. This meta-analysis revealed that using assays that evaluated multiple genes compared with single-gene assays did not increase the sensitivity or specificity of stool DNA testing in detecting CRC.
机译:这项荟萃分析旨在评估粪便DNA检测对结直肠癌(CRC)的诊断性能,并比较单基因和多基因检测之间的性能。使用关键词结直肠癌,粪便/粪便,敏感性,特异性,DNA和筛选来搜索MEDLINE,Cochrane,EMBASE数据库。对纳入的研究进行了敏感性分析,质量评估和性能偏倚。分析中包括53项研究,样本总数为7524名患者。对于CRC的粪便遗传生物标志物所分析的基因以及每种测定所使用的实验室方法,研究是异质的。不同测定的灵敏度范围为2%至100%,特异性范围为81%至100%。荟萃分析发现,单基因和多基因检测的合并敏感性分别为48.0%和77.8%,而合并特异性为97.0%和92.7%。接收者的操作曲线和诊断比值比在敏感性或特异性方面均未显示出显着差异。这项荟萃分析显示,与单基因分析相比,使用评估多个基因的分析不会增加粪便DNA检测在检测CRC中的敏感性或特异性。

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