Stool DNA testing for cancer surveillance in inflammatory bowel disease: an early view

被引:11
作者
Kisiel, John B. [1 ]
Ahlquist, David A. [1 ]
机构
[1] Mayo Clin, Div Gastroenterol & Hepatol, Rochester, MN 55905 USA
关键词
colorectal neoplasms; DNA methylation; early detection of cancer; inflammatory bowel disease; stool DNA; CHRONIC ULCERATIVE-COLITIS; CPG ISLAND METHYLATION; COLORECTAL-CANCER; COLONOSCOPIC SURVEILLANCE; NEOPLASTIC PROGRESSION; GENETIC ALTERATIONS; COST-EFFECTIVENESS; COLON-CANCER; BARRETTS-ESOPHAGUS; SPORADIC ADENOMAS;
D O I
10.1177/1756283X13487941
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Patients with inflammatory bowel disease (IBD) are at increased risk for colorectal cancer (CRC). Despite weak supporting evidence, important logistic barriers and high cost, colonoscopy is currently the only recommended approach to CRC surveillance in patients with IBD. As such, there is imperative to explore alternative or complementary strategies with potential to improve the efficiency and effectiveness of surveillance in IBD. Given our increasing understanding of tumorigenesis in IBD and the accompanying cascade of molecular alterations, there is a strong rationale to pursue biomarker assays for this application. Stoolbased DNA testing with advanced technology has been shown to be highly discriminatory for detection of sporadic colorectal cancer and advanced precancers. In early observations, stool DNA testing also shows promise for the accurate detection of IBD-associated colorectal neoplasms. These findings raise important clinical and translational questions about how to best evaluate and develop this technology, and devise clinical algorithms that will complement colonoscopy to improve patient outcomes.
引用
收藏
页码:371 / 380
页数:10
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