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. 2023 Apr 15;152(8):1536-1546.
doi: 10.1002/ijc.34373. Epub 2022 Dec 1.

Factors associated with interval colorectal cancer after negative FIT: Results of two screening rounds in the Dutch FIT-based CRC screening program

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Factors associated with interval colorectal cancer after negative FIT: Results of two screening rounds in the Dutch FIT-based CRC screening program

Emilie C H Breekveldt et al. Int J Cancer. .

Abstract

The interval colorectal cancer (CRC) rate after negative fecal immunochemical testing (FIT) is an important quality indicator of CRC screening programs. We analyzed the outcomes of two rounds of the FIT-based CRC screening program in the Netherlands, using data from individuals who participated in FIT-screening from 2014 to 2017. Data of individuals with one prior negative FIT (first round) or two prior negative FITs (first and second round) were included. Outcomes included the incidence of interval CRC in FIT-negative participants (<47 μg Hb/g feces [μg/g]), FIT-sensitivity, and the probability of detecting an interval CRC by fecal hemoglobin concentration (f-Hb). FIT-sensitivity was estimated using the detection method and the proportional incidence method (based on expected CRC incidence). Logistic regression analysis was performed to estimate whether f-Hb affects probability of detecting interval CRC, adjusted for sex- and age-differences. Incidence of interval CRC was 10.4 per 10 000 participants after the first and 9.6 after the second screening round. FIT-sensitivity based on the detection method was 84.4% (95%CI 83.8-85.0) in the first and 73.5% (95% CI 71.8-75.2) in the second screening round. The proportional incidence method resulted in a FIT-sensitivity of 76.4% (95%CI 73.3-79.6) in the first and 79.1% (95%CI 73.7-85.3) in the second screening round. After one negative FIT, participants with f-Hb just below the cut-off (>40-46.9 μg/g) had a higher probability of detecting an interval CRC (OR 16.9; 95%CI: 14.0-20.4) than had participants with unmeasurable f-Hb (0-2.6 μg/g). After two screening rounds, the odds ratio for interval CRC was 12.0 (95%CI: 7.8-17.6) for participants with f-Hb just below the cut-off compared with participants with unmeasurable f-Hb. After both screening rounds, the Dutch CRC screening program had a low incidence of interval CRC and an associated high FIT-sensitivity. Our findings suggest there is a potential for further optimizing CRC screening programs with the use of risk-stratified CRC screening based on prior f-Hb.

Keywords: colorectal cancer; colorectal cancer screening; fecal immunochemical testing.

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Conflict of interest statement

Manon C. W. Spaander receives financial research support from Sysmex/Sentinel; FIT tubes and analyses for research are provided. All other authors declare no conflicts of interest.

Figures

FIGURE 1
FIGURE 1
Flowchart displaying numbers for first and second round. CRC, colorectal cancer; FIT, fecal immunochemical test; SD‐CRC, screening‐detected colorectal cancer
FIGURE 2
FIGURE 2
(A) Stage distribution interval and screening‐detected cancers after the first round. (B) Stage distribution interval and screening‐detected cancers after the second round
FIGURE 3
FIGURE 3
(A) Localization interval and screening‐detected cancers after the first round. (B) Localization interval and screening‐detected cancers after the second round
FIGURE 4
FIGURE 4
(A) Probability of detecting interval CRCs after the first round by subgroups of f‐Hb concentrations. (B) Probability of detecting interval CRCs after the second round by subgroups of f‐Hb concentrations

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References

    1. Moss S, Ancelle‐Park R, Brenner H, International Agency for Research on Cancer . European guidelines for quality assurance in colorectal cancer screening and diagnosis. First edition‐‐evaluation and interpretation of screening outcomes. Endoscopy. 2012;44(Suppl 3):SE49‐SE64. doi:10.1055/s-0032-1309788 - DOI - PubMed
    1. Grobbee EJ, Schreuders EH, Hansen BE, et al. Association between concentrations of hemoglobin determined by fecal immunochemical tests and long‐term development of advanced colorectal neoplasia. Gastroenterology. 2017;153(5):1251‐1259.e2. doi:10.1053/j.gastro.2017.07.034 - DOI - PubMed
    1. Liao CS, Lin YM, Chang HC, et al. Application of quantitative estimates of fecal hemoglobin concentration for risk prediction of colorectal neoplasia. World J Gastroenterol. 2013;19(45):8366‐8372. doi:10.3748/wjg.v19.i45.8366 - DOI - PMC - PubMed
    1. van de Veerdonk W, van Hal G, Peeters M, De Brabander I, Silversmit G, Hoeck S. Risk stratification for colorectal neoplasia detection in the Flemish colorectal cancer screening program. Cancer Epidemiol. 2018;56:90‐96. doi:10.1016/j.canep.2018.07.015 - DOI - PubMed
    1. Toes‐Zoutendijk E, Kooyker AI, Dekker E, et al. Incidence of interval colorectal cancer after negative results from first‐round fecal immunochemical screening tests, by cutoff value and participant sex and age. Clin Gastroenterol Hepatol. 2020;18(7):1493‐1500. doi:10.1016/j.cgh.2019.08.021 - DOI - PubMed

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