Advances in Fecal Occult Blood Tests: the FIT revolution

Graeme P Young, Erin L Symonds, James E Allison, Stephen R Cole, Callum G Fraser, Stephen P Halloran, Ernst J Kuipers, Helen E Seaman, Graeme P Young, Erin L Symonds, James E Allison, Stephen R Cole, Callum G Fraser, Stephen P Halloran, Ernst J Kuipers, Helen E Seaman

Abstract

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.

Figures

Fig. 1
Fig. 1
Key steps in screening, each of which needs to be completed with high quality for there to be an impact on mortality from and/or incidence of CRC
Fig. 2
Fig. 2
Theoretical representation of distribution of fecal hemoglobin concentrations in normal subjects and cancer cases. The arrows labeled a, b and c point to different fecal hemoglobin concentrations (criterion values) which might be chosen to discrimination between those without pathology (normal) and those with cancer. At c, most normals are declared negative (hence a high specificity) and a majority but not all cancers are declared positive, while at a, most cancers are included (high sensitivity) but more normals will test positive
Fig. 3
Fig. 3
Reported sensitivity and specificity for CRC of a range of gFOBT [–58]
Fig. 4
Fig. 4
Reported sensitivity and specificity for CRC of a range of FIT [, , , , , –66]

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