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本文引用的文献

1
DNA methylation and cancer: ghosts and angels above the genes.DNA 甲基化与癌症:基因之上的鬼魅与天使。
Curr Opin Oncol. 2011 Jan;23(1):69-76. doi: 10.1097/CCO.0b013e3283412eb4.
2
Surveillance of screening-detected cancers (colon and rectum, breast, and cervix) - United States, 2004-2006.筛查发现癌症(结肠和直肠、乳腺、子宫颈)监测-美国,2004-2006 年。
MMWR Surveill Summ. 2010 Nov 26;59(9):1-25.
3
Longitudinal adherence with fecal occult blood test screening in community practice.社区实践中粪便潜血试验筛查的纵向依从性。
Ann Fam Med. 2010 Sep-Oct;8(5):397-401. doi: 10.1370/afm.1133.
4
Enhancing the use and quality of colorectal cancer screening.提高结直肠癌筛查的利用率和质量。
Evid Rep Technol Assess (Full Rep). 2010 Feb(190):1-195, v.
5
Clinical validity: defining biomarker performance.临床有效性:定义生物标志物性能。
Scand J Clin Lab Invest Suppl. 2010;242:46-52. doi: 10.3109/00365513.2010.493383.
6
Effect of verification bias on the sensitivity of fecal occult blood testing: a meta-analysis.粪便潜血检测中验证偏倚对其敏感性的影响:一项荟萃分析。
J Gen Intern Med. 2010 Nov;25(11):1211-21. doi: 10.1007/s11606-010-1375-0. Epub 2010 May 25.
7
Molecular detection of colorectal neoplasia.结直肠肿瘤的分子检测。
Gastroenterology. 2010 Jun;138(6):2127-39. doi: 10.1053/j.gastro.2010.01.055.
8
Systematic review: enhancing the use and quality of colorectal cancer screening.系统评价:提高结直肠癌筛查的使用和质量。
Ann Intern Med. 2010 May 18;152(10):668-76. doi: 10.7326/0003-4819-152-10-201005180-00239. Epub 2010 Apr 13.
9
Selective colorectal cancer screening in average-risk populations.一般风险人群的选择性结直肠癌筛查。
Rev Esp Enferm Dig. 2009 Dec;101(12):821-9. doi: 10.4321/s1130-01082009001200001.
10
NCCN clinical practice guidelines in oncology. Colorectal cancer screening.美国国立综合癌症网络(NCCN)肿瘤学临床实践指南。结直肠癌筛查
J Natl Compr Canc Netw. 2010 Jan;8(1):8-61. doi: 10.6004/jnccn.2010.0003.

用于结直肠癌筛查的粪便DNA检测:ColoSure™检测

Fecal DNA testing for Colorectal Cancer Screening: the ColoSure™ test.

作者信息

Ned Renée M, Melillo Stephanie, Marrone Michael

机构信息

Office of Public Health Genomics, Centers for Disease Control and Prevention.

出版信息

PLoS Curr. 2011 Mar 22;3:RRN1220. doi: 10.1371/currents.RRN1220.

DOI:10.1371/currents.RRN1220
PMID:21487548
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3050633/
Abstract

Colorectal cancer is the third most common cancer and the second leading cause of cancer-related deaths in the United States. Screening has been shown to be effective in reducing colorectal cancer incidence and mortality. Colonoscopy, sigmoidoscopy, and fecal occult blood tests are all recommended screening tests that have widespread availability. Nevertheless, many people do not receive the evidence-based recommended screening for colorectal cancer. Additional stool-based methods have been developed that offer more options for colorectal cancer screening, including a variety of fecal DNA tests. The only fecal DNA test that is currently available commercially in the United States is ColoSure(TM), which is marketed as a non-invasive test that detects an epigenetic marker (methylated vimentin) associated with colorectal cancer and pre-cancerous adenomas. We examined the published literature on the analytic validity, clinical validity, and clinical utility of ColoSure and we briefly summarized the current colorectal cancer screening guidelines regarding fecal DNA testing. We also addressed the public health implications of the test and contextual issues surrounding the integration of fecal DNA testing into current colorectal cancer screening strategies. The primary goal was to provide a basic overview of ColoSure and identify gaps in knowledge and evidence that affect the recommendation and adoption of the test in colorectal cancer screening strategies.

摘要

结直肠癌是美国第三大常见癌症,也是癌症相关死亡的第二大主要原因。筛查已被证明在降低结直肠癌发病率和死亡率方面是有效的。结肠镜检查、乙状结肠镜检查和粪便潜血试验都是推荐的筛查方法,广泛可用。然而,许多人没有接受基于证据的结直肠癌推荐筛查。已经开发出了更多基于粪便的方法,为结直肠癌筛查提供了更多选择,包括各种粪便DNA检测。目前在美国市场上唯一可买到的粪便DNA检测产品是ColoSure™,它被宣传为一种非侵入性检测,可检测与结直肠癌和癌前腺瘤相关的一种表观遗传标记(甲基化波形蛋白)。我们查阅了已发表的关于ColoSure分析有效性、临床有效性和临床实用性的文献,并简要总结了当前关于粪便DNA检测的结直肠癌筛查指南。我们还讨论了该检测对公共卫生的影响以及围绕将粪便DNA检测纳入当前结直肠癌筛查策略的相关背景问题。主要目标是提供ColoSure的基本概述,并找出影响该检测在结直肠癌筛查策略中的推荐和应用的知识和证据空白。