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首页> 外文期刊>The lancet oncology >Baseline faecal occult blood concentration as a predictor of incident colorectal neoplasia: longitudinal follow-up of a Taiwanese population-based colorectal cancer screening cohort.
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Baseline faecal occult blood concentration as a predictor of incident colorectal neoplasia: longitudinal follow-up of a Taiwanese population-based colorectal cancer screening cohort.

机译:基线粪便潜血浓度可预测结直肠癌的发生:台湾人群基于结直肠癌筛查队列的纵向随访。

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BACKGROUND: Despite widespread use of the immunochemical faecal occult blood test (iFOBT), little is known about the subsequent risk of developing colorectal neoplasia for participants with negative iFOBT results. We investigated whether the concentration of faecal haemoglobin at the first screen is predictive of the subsequent incidence of colorectal neoplasia in those with a negative screening result. METHODS: Between 2001 and 2007, we did a prospective cohort study within the Keelung community-based iFOBT screening programme for residents aged 40-69 years, using a cutoff faecal haemoglobin concentration of 100 ng/mL to classify attendees as negative and positive groups for further clinical investigations. 44,324 participants with negative findings and 1668 with a positive result at the first screen (854 non-referrals who refused colonoscopy and 814 with a false-positive result as assessed by colonoscopy) were followed up to ascertain cases of colorectal neoplasia. We investigated the association between baseline faecal haemoglobin concentration and risk of incident colorectal neoplasia, after adjusting for possible confounders. FINDINGS: Median follow-up was 4.39 years (IQR 2.53-6.12) for all 45 992 participants, during which the incidence of colorectal neoplasia increased from 1.74 per 1000 person-years for those with baseline faecal haemoglobin concentration 1-19 ng/mL, to 7.08 per 1000 person-years for those with a baseline concentration of 80-99 ng/mL. The adjusted hazard ratios (HRs) increased from 1.43 (95% CI 1.08-1.88) for baseline faecal haemoglobin concentration of 20-39 ng/mL, to 3.41 (2.02-5.75) for a baseline concentration of 80-99 ng/mL (trend test p<0.0001), relative to 1-19 ng/mL. These results did not change when we included repeated iFOBT measurements. Non-referrals had the highest risk of incident colorectal neoplasia (adjusted HR 8.46 [6.08-11.76]). INTERPRETATION: Quantitative faecal haemoglobin concentration at first screening predicts subsequent risk of incident colorectal neoplasia. During follow-up, risk stratification based on faecal haemoglobin could help clinicians, with particular attention being paid to those with higher initial faecal haemoglobin concentrations, especially those just under the threshold taken to indicate presence of colorectal neoplasia. FUNDING: None.
机译:背景:尽管免疫化学粪便潜血试验(iFOBT)的广泛使用,但对于iFOBT结果阴性的参与者随后发生结直肠瘤形成的风险知之甚少。我们调查了筛查结果为阴性的人在第一次筛查中的粪便血红蛋白浓度是否可预测大肠肿瘤的后续发生率。方法:在2001年至2007年之间,我们在基隆市社区iFOBT筛查计划中对40-69岁的居民进行了一项前瞻性队列研究,使用截断浓度为100 ng / mL的粪便血红蛋白将参与者分为阴性和阳性人群。进一步的临床研究。在首次筛查中有44324名阴性结果参与者和1668名阳性结果参与者(854名拒绝结肠镜检查的非转诊患者和814名结肠镜检查结果为假阳性的患者)得到随访,以确定结直肠癌的病例。在调整可能的混杂因素后,我们调查了基线粪便血红蛋白浓度与发生大肠肿瘤的风险之间的关联。结果:所有45 992名参与者的中位随访时间为4.39年(IQR 2.53-6.12),在此期间,粪便血红蛋白基线浓度为1-19 ng / mL的人群大肠肿瘤的发生率从每1000人年1.74例增加,基线浓度为80-99 ng / mL的人群,每千人年可增加到7.08。调整后的危险比(HRs)从基线粪便血红蛋白浓度为20-39 ng / mL的1.43(95%CI 1.08-1.88)增加到基线浓度为80-99 ng / mL的3.41(2.02-5.75)(趋势测试p <0.0001),相对于1-19 ng / mL。当我们包括重复的iFOBT测量结果时,这些结果没有改变。不推荐转诊的人发生结直肠癌的风险最高(校正后的HR 8.46 [6.08-11.76])。解释:首次筛查时粪便中血红蛋白的定量预测了随后发生大肠癌的风险。在随访期间,基于粪便血红蛋白的风险分层可以为临床医生提供帮助,尤其要注意那些初始粪便血红蛋白浓度较高的患者,尤其是那些刚好低于表明存在大肠肿瘤的阈值的患者。资金:无。

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