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达到筛查年龄上限后的间期癌风险:基于粪便免疫化学检测的结直肠癌筛查中的风险分层告知

Interval cancer risk after the upper age limit of screening has been reached: Informing risk stratification in FIT-based colorectal cancer screening.

作者信息

van Stigt Brenda J, Lansdorp-Vogelaar Iris, Spaander Manon C W, van Vuuren Anneke J, Dekker Evelien, van Kemenade Folkert J, Nagtegaal Iris D, van Leerdam Monique E, Toes-Zoutendijk Esther

机构信息

Department of Public Health, Erasmus MC University Medical Centre, Rotterdam, The Netherlands.

Department of Gastroenterology and Hepatology, Erasmus MC University Medical Centre, Rotterdam, The Netherlands.

出版信息

Int J Cancer. 2025 May 1;156(9):1783-1790. doi: 10.1002/ijc.35294. Epub 2024 Dec 19.

Abstract

Upper age limits are currently fixed for all fecal immunochemical test (FIT)-based colorectal cancer (CRC) screening programs. A risk-stratified upper age limit may be beneficial. Therefore, we assessed differences in interval CRC risk among individuals who had reached the upper age limit of screening (75 years). Individuals with a negative FIT (<47 μg Hb/g feces) in the final round of the Dutch CRC screening program were selected from the national screening database and linked to the national cancer registry to identify CRCs diagnosed within 24 months (interval CRCs). Survival analyses assessed whether sex and last fecal hemoglobin (f-Hb) concentration were associated with interval CRC risk. A multivariable logistic regression assessed whether sex, last f-Hb concentration and screening round were associated with stage distribution (early vs. late). Last f-Hb concentrations were considered detectable when they were >0 μg Hb/g feces. Among 305,761 individuals with a complete follow-up (24 months), 661 were diagnosed with interval CRC (21.6 per 10,000 negative FITs). Individuals with detectable f-Hb (15%) were 5 times more likely to be diagnosed with interval CRC than those without (HR 4.87, 95%CI: 4.19-5.65). Moreover, their cancers were more often detected at a late stage compared to individuals without detectable f-Hb (OR 1.45, 95%CI: 1.06-2.01). Our results show that interval CRC risk among individuals aged ≥75 differs substantially by last f-Hb concentration, indicating a uniform age to stop screening is suboptimal. Future research, taking into account multiple screening rounds and FIT results, should determine the optimal risk-stratified screening strategy.

摘要

目前,所有基于粪便免疫化学检测(FIT)的结直肠癌(CRC)筛查项目都设定了年龄上限。风险分层的年龄上限可能会更有益。因此,我们评估了达到筛查年龄上限(75岁)的个体之间间隔期结直肠癌风险的差异。从荷兰全国筛查数据库中选取了在荷兰CRC筛查项目最后一轮中FIT结果为阴性(<47μg血红蛋白/克粪便)的个体,并与国家癌症登记处进行关联,以确定在24个月内诊断出的CRC(间隔期CRC)。生存分析评估了性别和末次粪便血红蛋白(f-Hb)浓度是否与间隔期CRC风险相关。多变量逻辑回归评估了性别、末次f-Hb浓度和筛查轮次是否与分期分布(早期与晚期)相关。当末次f-Hb浓度>0μg血红蛋白/克粪便时,认为其可检测。在305,761名有完整随访(24个月)的个体中,661人被诊断为间隔期CRC(每10,000次FIT阴性中有21.6例)。f-Hb可检测的个体(15%)被诊断为间隔期CRC的可能性是f-Hb不可检测个体的5倍(风险比4.87,95%置信区间:4.19-5.65)。此外,与f-Hb不可检测的个体相比,他们的癌症更常被诊断为晚期(比值比1.45,95%置信区间:1.06-2.01)。我们的结果表明,年龄≥75岁个体的间隔期CRC风险因末次f-Hb浓度而有很大差异,这表明统一的停止筛查年龄并非最佳选择。未来的研究应考虑多次筛查轮次和FIT结果,以确定最佳的风险分层筛查策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f216/11887016/f935bc10c4f1/IJC-156-1783-g002.jpg

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