Performance of Faecal Immunochemical Testing for Colorectal Cancer Screening at Varying Positivity Thresholds.

IF 6.6 1区 医学 Q1 GASTROENTEROLOGY & HEPATOLOGY Alimentary Pharmacology & Therapeutics Pub Date : 2024-10-07 DOI:10.1111/apt.18314
Kristin Ranheim Randel, Edoardo Botteri, Thomas de Lange, Anna Lisa Schult, Sigrun Losada Eskeland, Badboni El-Safadi, Espen R Norvard, Nils Bolstad, Michael Bretthauer, Geir Hoff, Øyvind Holme
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Abstract

Background: The positivity thresholds of faecal immunochemical testing (FIT) in colorectal cancer (CRC) screening vary between countries.

Aims: To explore the trade-off between colonoscopies performed, adverse events and lesions detected at different FIT thresholds in a Norwegian CRC screening trial.

Methods: We included first participation in biennial FIT screening for 47,265 individuals aged 50-74 years. Individuals with FIT > 15 μg Hb/g faeces were referred for colonoscopy. We estimated the number of colonoscopies, adverse events, screen-detected CRCs, advanced adenomas and serrated lesions expected at FIT thresholds currently or recently used in other European countries ranging between 20 and 150 μg/g.

Results: At the 15 μg/g threshold (Norway), 3705 participants underwent colonoscopy, of whom 203 had CRC, 1119 advanced adenomas and 256 advanced serrated lesions. Using a 47 μg/g threshold, 1826 (49.3%) individuals would have undergone colonoscopy, and 154 (75.9%) would have been diagnosed with CRC, 702 (62.7%) with advanced adenoma and 128 (50.0%) with advanced serrated lesion compared to the 15 μg/g threshold. At 150 μg/g, the corresponding figures would have been 838 (22.6%) undergoing colonoscopy, 114 (56.2%) with CRC, 345 (30.8%) advanced adenoma and 54 (21.1%) advanced serrated lesions. The detection rate of stage I CRC was 0.22% at 15 μg/g and 0.11% at 150 μg/g. Post-colonoscopy bleeding rates were 0.8% and 1.7%, respectively.

Conclusions: Increasing the FIT threshold reduces colonoscopy demand, but substantially decreases lesion detection and unfavourably changes CRC stage distribution. The risk of adverse events at colonoscopy increased with FIT threshold, requiring country-specific information on adverse events.

Trial registration: Clinicaltrials.gov identifier: NCT01538550.

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粪便免疫化学检验在不同阳性阈值下筛查结直肠癌的性能。
背景:粪便免疫化学检验(FIT)在大肠癌筛查中的阳性阈值因国家而异:目的:在挪威的一项 CRC 筛查试验中,探讨不同 FIT 临界值下结肠镜检查、不良事件和病变检测之间的权衡:我们纳入了首次参加两年一次的 FIT 筛查的 47,265 名 50-74 岁的患者。FIT > 15 μg Hb/g粪便的患者将被转诊接受结肠镜检查。我们估算了在其他欧洲国家目前或最近使用的 20 至 150 μg/g 的 FIT 阈值下,预计结肠镜检查、不良事件、筛查出的 CRC、晚期腺瘤和锯齿状病变的数量:在 15 μg/g 临界值(挪威)下,3705 人接受了结肠镜检查,其中 203 人患有 CRC,1119 人患有晚期腺瘤,256 人患有晚期锯齿状病变。与 15 微克/克的阈值相比,如果采用 47 微克/克的阈值,将有 1826 人(49.3%)接受结肠镜检查,154 人(75.9%)被诊断为 CRC,702 人(62.7%)被诊断为晚期腺瘤,128 人(50.0%)被诊断为晚期锯齿状病变。在 150 微克/克的临界值下,接受结肠镜检查的人数为 838 人(22.6%),其中 114 人(56.2%)患有 CRC,345 人(30.8%)为晚期腺瘤,54 人(21.1%)为晚期锯齿状病变。15 微克/克的 CRC I 期检出率为 0.22%,150 微克/克的检出率为 0.11%。结肠镜检查后出血率分别为 0.8% 和 1.7%:结论:提高 FIT 临界值可减少结肠镜检查需求,但会大幅降低病变检出率,并不利地改变 CRC 分期分布。结肠镜检查中发生不良事件的风险随着FIT阈值的提高而增加,因此需要针对不同国家的不良事件信息:试验注册:Clinicaltrials.gov identifier:试验注册:Clinicaltrials.gov identifier:NCT01538550。
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来源期刊
CiteScore
15.60
自引率
7.90%
发文量
527
审稿时长
3-6 weeks
期刊介绍: Alimentary Pharmacology & Therapeutics is a global pharmacology journal focused on the impact of drugs on the human gastrointestinal and hepato-biliary systems. It covers a diverse range of topics, often with immediate clinical relevance to its readership.
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