Department of Internal Medicine, College of Medicine, Ewha Womans University, Seoul, Republic of Korea.
Department of Internal Medicine, Hanyang University Guri Hospital, Guri, Republic of Korea.
Dig Liver Dis. 2018 Aug;50(8):847-852. doi: 10.1016/j.dld.2018.04.001. Epub 2018 Apr 11.
The clinical significance of diminutive or small adenomas remains ill defined.
We evaluated the clinical impact of diminutive or small adenomas at baseline on the risk of developing metachronous advanced colorectal neoplasia (CRN).
This multicenter, retrospective cohort study included 2252 patients with 1 or more colorectal adenomas at baseline and subsequent follow-up colonoscopy. Baseline colonoscopy findings were classified into 5 groups: 1 or 2 tubular adenomas (TAs) (<10 mm); 3-10 diminutive TAs (≤5 mm); 3-10 TAs, including 1 or 2 small adenomas (6-10 mm); 3-10 TAs, including 3 or more small adenomas; and advanced adenoma.
In multivariate analysis, after adjusting for possible confounding variables (age at baseline, sex, body mass index, smoking habits, family history of colorectal cancer, regular use of aspirin or NSAIDs, and adenoma location), 3-10 TAs including 3 or more small adenomas (hazard ratio [HR] = 2.36, p = 0.034) and advanced adenoma (HR = 2.14, p < 0.001) were independent predictors for the risk of developing metachronous advanced CRN. However, 3-10 diminutive TAs or 3-10 TAs, including 1 or 2 small adenomas, were not associated with this outcome.
Multiplicity of diminutive TAs, without advanced lesions, showed no clinical significance for risk of developing metachronous advanced CRN.
小或微小腺瘤的临床意义仍未明确。
我们评估了基线时小或微小腺瘤对发生异时性高级结直肠腺瘤性病变(CRN)风险的临床影响。
这是一项多中心、回顾性队列研究,纳入了基线时存在 1 个或多个结直肠腺瘤且随后行结肠镜随访的 2252 例患者。基线结肠镜检查结果分为 5 组:1 或 2 个管状腺瘤(TA)(<10mm);3-10 个微小 TA(≤5mm);3-10 个 TA,包括 1 或 2 个小腺瘤(6-10mm);3-10 个 TA,包括 3 个或更多小腺瘤;以及高级腺瘤。
多变量分析调整了可能的混杂因素(基线时年龄、性别、体重指数、吸烟习惯、结直肠癌家族史、阿司匹林或 NSAIDs 的常规使用以及腺瘤位置)后,包括 3 个或更多小腺瘤的 3-10 个 TA(风险比 [HR] = 2.36,p = 0.034)和高级腺瘤(HR = 2.14,p < 0.001)是发生异时性高级 CRN 的独立预测因素。然而,3-10 个微小 TA 或包括 1 或 2 个小腺瘤的 3-10 个 TA 与该结果无关。
无高级病变的微小 TA 的多发性对发生异时性高级 CRN 的风险没有临床意义。