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Faecal immunochemical testing (FIT) in symptomatic patients: what are we missing?
Alexia Farrugia1,2, Monika Widlak2,3, Charles Evans1
1Department of Surgery, University Hospitals Coventry and Warwickshire NHS Trust, Coventry, UK.
The faecal immunochemical test (FIT) is a promising triage tool for colorectal cancer (CRC) in symptomatic patients. While FIT shows high sensitivity and specificity within NICE guidelines, a miss rate necessitates further investigation for higher-risk groups.
Area of Science:
- Gastroenterology
- Oncology
- Clinical Diagnostics
Background:
- Faecal immunochemical test (FIT) is a non-invasive method for detecting colorectal cancer (CRC).
- Recent National Institute for Health and Care Excellence (NICE) guidelines (NG12 and DG30) provide frameworks for CRC triage.
- Symptomatic patients are a key population for CRC screening and early detection.
Purpose of the Study:
- To evaluate the effectiveness of FIT as a triage test for colorectal cancer (CRC).
- To assess FIT performance within the NG12 and DG30 NICE guidelines for symptomatic patients.
- To determine the sensitivity and specificity of FIT in identifying CRC and adenomas.
Main Methods:
- A single-centre prospective study was conducted on patients referred via the 2-week wait (TWW) pathway.
- Data from 612 patients were analyzed, categorizing them by NG12 (n=519) and DG30 (n=79) criteria.
- FIT was performed on all patients, with sensitivity, specificity, and predictive values calculated for CRC and adenomas.
Main Results:
- CRC sensitivity was 84.85% for NG12 and 100% for DG30. Specificity was 81.28% for NG12 and 91.89% for DG30.
- Adenoma sensitivity was approximately 30.77% for NG12 and 25% for DG30.
- FIT demonstrated high sensitivity and specificity within the NG12 pathway, with excellent sensitivity and improved specificity in the DG30 group.
Conclusions:
- FIT is an effective triage tool for CRC within the NG12 NICE guidelines, despite a residual miss rate.
- FIT shows excellent sensitivity and improved specificity for DG30, though this pathway targets lower-risk individuals.
- For the higher-risk NG12 group, additional tests or markers may be needed to minimize missed CRC cases.
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