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Evaluation of Colorectal Cancer Risk and Prevalence by Stool DNA Integrity Detection
Published on: June 8, 2020
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Interval colorectal cancers after negative faecal immunochemical test in a 13-year screening programme
Manuel Zorzi1, Cesare Hassan2, Carlo Senore3
1Veneto Tumour Registry, Azienda Zero, Padova, Italy.
Journal of Medical Screening
|May 13, 2020
Summary
The faecal immunochemical test (FIT) shows high sensitivity for detecting cancer, exceeding 80% and leading to fewer interval colorectal cancers. Sensitivity improved with repeat screening rounds.
Area of Science:
- Gastroenterology
- Oncology
- Public Health
Background:
- Colorectal cancer (CRC) screening programs aim to detect cancer early.
- The faecal immunochemical test (FIT) is a widely used screening tool.
- Understanding FIT sensitivity, especially for interval cancers, is crucial for program evaluation.
Purpose of the Study:
- To assess the sensitivity of the faecal immunochemical test (FIT) for cancer detection.
- To evaluate FIT performance over six rounds of biennial screening in a large population.
- To analyze interval colorectal cancer rates and their relationship with FIT sensitivity.
Main Methods:
- A population-based cohort of 123,347 individuals aged 50-69 was followed from 2002 to 2015.
- Four hundred forty-one thousand, six hundred forty-seven FITs were administered over six biennial screening rounds.
- Test sensitivity was calculated using the Proportional Interval Cancer Rate and Interval Cancer Proportion methods.
Main Results:
- An interval colorectal cancer incidence rate of 1.87 per 10,000 person-years was observed.
- Overall FIT sensitivity was 86.9% (Proportional Interval Cancer Rate) and 83.9% (Interval Cancer Proportion).
- Sensitivity was lowest in the first round and increased with subsequent screening rounds.
Conclusions:
- High FIT sensitivity (over 80%) is associated with a low incidence of interval colorectal cancers.
- FIT demonstrates effective cancer detection, highlighting its value in screening programs.
- Methodological differences in calculating sensitivity led to varying trends across screening rounds.
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