Advances in Fecal Occult Blood Tests: The FIT Revolution

被引:0
|
作者
Graeme P. Young
Erin L. Symonds
James E. Allison
Stephen R. Cole
Callum G. Fraser
Stephen P. Halloran
Ernst J. Kuipers
Helen E. Seaman
机构
[1] Flinders University,Flinders Centre for Innovation in Cancer L3:100
[2] Repatriation General Hospital,Bowel Health Service
[3] University of California,Division of Gastroenterology
[4] San Francisco (UCSF),Ninewells Hospital and Medical School, Centre for Research into Cancer Prevention and Screening
[5] San Francisco General Hospital,Department of Biochemistry and Physiology, School of Biosciences and Medicine
[6] Scottish Bowel Screening Research Unit,undefined
[7] University of Dundee,undefined
[8] NHS Bowel Cancer Screening Southern Programme Hub,undefined
[9] University of Surrey,undefined
[10] Erasmus MC University Medical Center Rotterdam,undefined
来源
Digestive Diseases and Sciences | 2015年 / 60卷
关键词
Colorectal cancer; Screening; Fecal occult blood test; FIT; Sensitivity; Specificity;
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中图分类号
学科分类号
摘要
There is a wide choice of fecal occult blood tests (FOBTs) for colorectal cancer screening. Goal: To highlight the issues applicable when choosing a FOBT, in particular which FOBT is best suited to the range of screening scenarios. Four scenarios characterize the constraints and expectations of screening programs: (1) limited colonoscopy resource with a need to constrain test positivity rate; (2) a priority for maximum colorectal neoplasia detection with little need to constrain colonoscopy workload; (3) an “adequate” endoscopy resource that allows balancing the benefits of detection with the burden of service provision; and (4) a need to maximize participation in screening. Guaiac-based FOBTs (gFOBTs) have significant deficiencies, and fecal immunochemical tests (FITs) for hemoglobin have emerged as better tests. gFOBTs are not sensitive to small bleeds, specificity can be affected by diet or drugs, participant acceptance can be low, laboratory quality control opportunities are limited, and they have a fixed hemoglobin concentration cutoff determining positivity. FITs are analytically more specific, capable of quantitation and hence provide flexibility to adjust cutoff concentration for positivity and the balance between sensitivity and specificity. FITs are clinically more sensitive for cancers and advanced adenomas, and because they are easier to use, acceptance rates are high. Conclusions: FOBT must be chosen carefully to meet the needs of the applicable screening scenario. Quantitative FIT can be adjusted to suit Scenarios 1, 2 and 3, and for each, they are the test of choice. FITs are superior to gFOBT for Scenario 4 and gFOBT is only suitable for Scenario 1.
引用
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页码:609 / 622
页数:13
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