U1086 "ANTICIPE" INSERM-University of Caen Normandy, Centre François Baclesse, Caen, France.
Department of Hepato-Gastroenterology and Digestive Oncology, Rouen University Hospital, France.
Mol Oncol. 2024 Nov;18(11):2629-2648. doi: 10.1002/1878-0261.13734. Epub 2024 Sep 30.
Colorectal cancer (CRC) screening has been proven to reduce both mortality and the incidence of this disease. Most CRC screening programs are based on fecal immunochemical tests (FITs), which have a low participation rate. Searching for blood protein biomarkers can lead to the development of a more accepted screening test. The aim of this systematic review was to compare the diagnostic potential of the most promising serum protein biomarkers. A systematic review based on PRISMA guidelines was conducted in the PubMed and Web of Science databases between January 2010 and December 2023. Studies assessing blood protein biomarkers for CRC screening were included. The sensitivity, specificity, and area under the ROC curve of each biomarker were collected. Among 4685 screened studies, 94 were considered for analysis. Most of them were case-control studies, leading to an overestimation of the performance of candidate biomarkers. The performance of no protein biomarker or combination of biomarkers appears to match that of the FIT. Studies with a suitable design and population, testing new assay techniques, or based on algorithms combining FIT with serum tests are needed.
结直肠癌(CRC)筛查已被证明可降低死亡率和疾病发生率。大多数 CRC 筛查计划基于粪便免疫化学检测(FITs),但参与率较低。寻找血液蛋白生物标志物可开发出更易被接受的筛查检测方法。本系统评价旨在比较最有前途的血清蛋白生物标志物的诊断潜力。根据 PRISMA 指南,在 PubMed 和 Web of Science 数据库中对 2010 年 1 月至 2023 年 12 月期间发表的研究进行了系统评价。纳入评估血液蛋白生物标志物用于 CRC 筛查的研究。收集了每个生物标志物的敏感性、特异性和 ROC 曲线下面积。在筛选出的 4685 项研究中,有 94 项被认为适合分析。其中大多数是病例对照研究,这导致候选生物标志物的性能被高估。没有一种蛋白生物标志物或标志物组合的性能似乎与 FIT 相匹配。需要进行设计和人群合适、测试新检测技术或基于结合 FIT 和血清检测的算法的研究。