FIT is Superior to FOBT for Colorectal Cancer Screening
Fecal Immunochemical Test (FIT) is strongly recommended over guaiac-based Fecal Occult Blood Test (gFOBT) for colorectal cancer screening due to its superior sensitivity, comparable specificity, and higher patient adherence rates. 1
Diagnostic Performance Comparison
Sensitivity and Specificity
- FIT demonstrates significantly higher sensitivity for colorectal cancer detection (73-88%) compared to gFOBT (30-65%), essentially doubling the cancer detection capability while maintaining similar specificity. 2, 3
- Multiple studies show FIT's superior cancer detection sensitivity: 84.6% for FIT vs. 30.8% for gFOBT (Park et al.), and 100% for FIT vs. 54.2% for gFOBT (Parra-Blanco et al.). 1
- When threshold levels are adjusted to achieve similar positivity rates, FIT sensitivity for colorectal cancer remains twice as high as gFOBT (73.3% vs. 33.3%) with comparable specificity (>95%). 1
- For advanced neoplasia detection, FIT significantly outperforms gFOBT with a relative risk of 2.28 (95% CI, 1.68-3.10). 1
Technical Advantages
- FIT specifically detects human hemoglobin in stool, while gFOBT only detects heme, making FIT more specific for lower GI bleeding. 3, 4
- Unlike gFOBT, FIT is not affected by:
Patient Experience and Adherence
- FIT requires fewer stool samples (typically 1-2) compared to gFOBT (3 samples), significantly improving patient compliance. 1, 3
- Multiple randomized controlled trials show approximately 10-20% higher participation rates with FIT compared to gFOBT. 1
- Specific participation rate comparisons include:
Advanced Features of FIT
- Quantitative FITs allow for adjustment of hemoglobin concentration cutoff values to balance sensitivity and specificity based on available colonoscopy resources. 2, 3
- Lower cutoff values increase sensitivity for advanced adenomas but decrease specificity: decreasing from 20 to 10 μg/g increases sensitivity from 29% to 35%, with specificity decreasing from 97% to 93%. 2
- FIT has been incorporated into more advanced screening tests like multitarget stool DNA testing, which further improves sensitivity for cancer (92.3% vs. 73.8%) and advanced lesions (42.4% vs. 23.8%), though with lower specificity (86.6% vs. 94.9%). 1
Important Limitations and Caveats
- FIT has poor sensitivity (approximately 5%) for sessile serrated polyps, which are important precursors to colorectal cancer. 1, 3
- Any positive result from either test requires follow-up colonoscopy, not repeat testing, due to the high positive predictive value for cancer detection. 1
- Single-sample testing has lower sensitivity than multi-sample testing, highlighting the importance of proper test protocol. 3
- In-clinic FOBT performed during digital rectal examination is not recommended for colorectal cancer screening due to extremely poor sensitivity (<10%). 3
Implementation Considerations
- Programs implementing FIT should establish systems to track testing cycles and ensure appropriate follow-up of positive results. 1
- The superior performance characteristics of FIT make it the preferred non-invasive screening method for colorectal cancer, despite the availability of newer molecular biomarker tests that may have higher sensitivity but lower specificity and higher costs. 5
- Multiple rounds of FIT testing (annual or biennial) are recommended to maximize the effectiveness of cancer detection and prevention. 1, 2