Zhao Zitong, Zhu Anna, Bhardwaj Megha, Schrotz-King Petra, Brenner Hermann
Division of Clinical Epidemiology and Aging Research, German Cancer Research Center (DKFZ), 69120 Heidelberg, Germany.
Medical Faculty Heidelberg, University of Heidelberg, 69120 Heidelberg, Germany.
Cancers (Basel). 2021 Dec 23;14(1):65. doi: 10.3390/cancers14010065.
Colorectal cancer (CRC) is the third most common cancer and the second leading cause of cancer mortality globally. Fecal miRNAs have been suggested to be promising biomarkers for CRC early detection. We aimed to conduct a systematic literature review on the diagnostic performance of fecal miRNA markers for CRC and its precursors. PubMed and Web of Science were searched to retrieve relevant articles published up to 7 December 2021. Information on study design, characteristics of study population, pre-analytics (sample collection, processing, and storage), fecal miRNA extraction and quantification technologies, and diagnostic performance (including sensitivity, specificity, and area under the curve (AUC)) were summarized. Twenty studies reporting on 31 individual miRNAs and 16 miRNA panels (with 2-9 markers) for CRC diagnosis were identified. Substantial heterogeneity existed regarding stool sample collection, processing, storage, and miRNA extraction and normalization. For two individual miRNAs and one miRNA panel, values ≥ 80% were reported for both sensitivity and specificity; however, none of these results were either internally or externally validated. In a study among fecal immunochemical test-positive cases recruited from a true screening setting, better diagnostic performance was identified and internally validated for a combination panel including two miRNAs, fecal hemoglobin level, and patient age and sex, compared with fecal hemoglobin concentration alone. Fecal miRNAs or miRNA panels, possibly in combination with fecal hemoglobin test, may be promising candidates for noninvasive CRC early detection. However, large prospective and well-designed studies in CRC screening cohorts are required to validate promising miRNAs or miRNA panels.
结直肠癌(CRC)是全球第三大常见癌症,也是癌症死亡的第二大主要原因。粪便微小RNA(miRNA)被认为是CRC早期检测的有前景的生物标志物。我们旨在对粪便miRNA标志物用于CRC及其前驱病变的诊断性能进行系统的文献综述。检索了PubMed和Web of Science,以获取截至2021年12月7日发表的相关文章。总结了有关研究设计、研究人群特征、分析前(样本采集、处理和储存)、粪便miRNA提取和定量技术以及诊断性能(包括敏感性、特异性和曲线下面积(AUC))的信息。确定了20项关于31种单个miRNA和16个miRNA面板(含2 - 9个标志物)用于CRC诊断的研究。在粪便样本采集、处理、储存以及miRNA提取和标准化方面存在很大的异质性。对于两种单个miRNA和一个miRNA面板,报告的敏感性和特异性值均≥80%;然而,这些结果均未经过内部或外部验证。在一项从真实筛查环境中招募的粪便免疫化学检测阳性病例的研究中,与单独的粪便血红蛋白浓度相比,一个包含两种miRNA、粪便血红蛋白水平以及患者年龄和性别的联合面板显示出更好的诊断性能,并经过了内部验证。粪便miRNA或miRNA面板,可能与粪便血红蛋白检测相结合,可能是无创CRC早期检测的有前景的候选方法。然而,需要在CRC筛查队列中进行大型前瞻性和设计良好的研究,以验证有前景的miRNA或miRNA面板。