Lee Seung Min, Kim Jeong Hwan, Sung In Kyung, Hong Sung Noh
Department of Internal Medicine, Konkuk University School of Medicine, Seoul, Korea.
Department of Medicine, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Korea.
Gut Liver. 2015 Nov 23;9(6):741-9. doi: 10.5009/gnl14210.
BACKGROUND/AIMS: Colorectal adenomas that are ≥10 mm have villous histology or high-grade dysplasia, or that are associated with ≥3 adenomas are considered high-risk for metachronous advanced neoplasia. We evaluated the cumulative incidence of metachronous advanced neoplasia according to the total number of high-risk findings detected on baseline colonoscopy. METHODS: This was a retrospective cohort study performed in 862 patients who underwent removal of colorectal adenomas between 2005 and 2009. At least one surveillance colonoscopy had been conducted at Konkuk University Medical Center, Seoul, Korea. RESULTS: The cumulative incidence of metachronous advanced neoplasia in patients with 0, 1, 2, and 3-4 high-risk findings at 1 year were 0.7%, 1.3%, 2.8%, and 8.0%; at 3 years, those were 5.9%, 11.9%, 15.5%, and 24.7%; and at 5 years, those were 8.5%, 18.7%, 26.3%, and 37.2%, respectively. In a multivariate model, the risk of metachronous advanced neoplasia was significantly higher for the multiple high-risk findings group when compared with the 0 high-risk findings group (1 high-risk (+) hazard ratio, 1.86 [95% confidence interval, 1.00-3.44]; 2 high-risk (+) 1.84 [0.88-3.84]; and 3-4 high-risk (+) 3.29 [1.54-7.01]; ptrend=0.020). CONCLUSIONS: The presence of overlapping multiple high-risk findings was associated with an increased risk of advanced neoplasia during surveillance.
背景/目的:直径≥10mm、具有绒毛状组织学特征或高级别异型增生,或与≥3个腺瘤相关的结直肠腺瘤被认为发生异时性晚期肿瘤的风险较高。我们根据基线结肠镜检查发现的高危结果总数评估了异时性晚期肿瘤的累积发病率。 方法:这是一项回顾性队列研究,对2005年至2009年间接受结直肠腺瘤切除的862例患者进行。韩国首尔建国大学医学中心至少进行了一次监测结肠镜检查。 结果:在1年时,具有0、1、2和3 - 4个高危结果的患者中,异时性晚期肿瘤的累积发病率分别为0.7%、1.3%、2.8%和8.0%;在3年时,分别为5.9%、11.9%、15.5%和24.7%;在5年时,分别为8.5%、18.7%、26.3%和37.2%。在多变量模型中,与0个高危结果组相比,多个高危结果组发生异时性晚期肿瘤的风险显著更高(1个高危结果(+)风险比,1.86[95%置信区间,1.00 - 3.44];2个高危结果(+)1.84[0.88 - 3.84];3 - 4个高危结果(+)3.29[1.54 - 7.01];P趋势 = 0.020)。 结论:存在多个重叠的高危结果与监测期间晚期肿瘤风险增加相关。
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