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首页> 外文期刊>Clinical colorectal cancer >Review of Blood-Based Colorectal Cancer Screening: How Far Are Circulating Cell-Free DNA Methylation Markers From Clinical Implementation?
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Review of Blood-Based Colorectal Cancer Screening: How Far Are Circulating Cell-Free DNA Methylation Markers From Clinical Implementation?

机译:综述血基结肠直肠癌筛选:从临床实施中循环无细胞DNA甲基化标记的速度有多远?

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Colorectal cancer (CRC) is a leading cause of cancer related deaths worldwide, and late stages (III-IV) in particular have low 5-year survival rates. Stage shifting by CRC screening programs has proven effective by decreasing morbidity and mortality and in many countries national CRC screening programs have been implemented. Currently, European, Asian, and American authorities recommend screening for CRC using fecal occult blood testing, sigmoidoscopy, or colonoscopy. Because these approaches all have weaknesses (eg, poor compliance, high costs, test invasiveness), much effort has been put into the development of alternative screening approaches, many of which are blood-based. Blood-based strategies especially present the advantages of minimally invasiveness compared to endoscopies and an expectantly higher compliance rate compared to stool-based tests. The last decades have seen many discovery studies identifying promising blood-based biomarkers of CRC; however, common to all of these markers is that their clinical usefulness remains evasive. At present only one blood-based CRC screening marker has been approved in the United States. The aim of this review is to discuss the development of blood-based cell-free DNA methylation marker candidates for CRC screening. On the basis of a methodical literature search, the past, present, and future of cell-free DNA screening markers for CRC are revised and discussed. Resource limitations and technical challenges related to sensitivity and specificity measurements keep many markers at bay. Possible solutions to these problems are offered to enable markers to benefit future screening participants. (C) 2018 Elsevier Inc. All rights reserved.
机译:结肠直肠癌(CRC)是全球癌症相关死亡的主要原因,特别是5年生存率低的晚期阶段(III-IV)。 CRC筛查计划的阶段转移通过降低发病率和死亡率和死亡率,并且在许多国家的国家CRC筛查计划已经实施。目前,欧洲,亚洲和美国当局建议使用粪便隐血血液检测,Sigmoidopy或结肠镜检查筛选CRC。因为这些方法都有缺点(例如,合规性差,成本差,测试侵犯性,测试侵犯性差,所以已经投入了替代筛查方法的发展,其中许多是基于血液的。与内窥镜和基于粪便的测试相比,血液策略特别呈现最微弱的侵袭性和预期的合规率。过去几十年曾看到许多发现研究识别有前途的CRC的血液生物标志物;然而,所有这些标记的共同点是它们的临床用途仍然是避免的。目前只有一种基于血液的CRC筛查标记已在美国批准。本综述的目的是讨论CRC筛选的血基无细胞DNA甲基化标志物候选的开发。根据一种方法文献搜索,对CRC的无细胞DNA筛查标记物的过去,存在和未来进行了修订和讨论。与敏感性和特异性测量相关的资源限制和技术挑战在海湾保持许多标记。提供了这些问题的可能解决方案,以使标记能够利用未来的筛选参与者。 (c)2018年Elsevier Inc.保留所有权利。

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