Department of Gastroenterology and Hepatology, University Medical Center Utrecht, Utrecht, The Netherlands.
Division of Gastroenterology, Department of Medicine, Icahn School of Medicine at Mount Sinai, New York, New York; Division of Gastroenterology, Hepatology and Nutrition, Department of Medicine, Vanderbilt University Medical Center, Nashville, Tennessee.
Clin Gastroenterol Hepatol. 2020 Jun;18(7):1518-1527.e3. doi: 10.1016/j.cgh.2019.08.032. Epub 2019 Aug 22.
BACKGROUND & AIMS: Little is known about the clinical significance of indefinite dysplasia (IND) in patients with inflammatory bowel diseases (IBD) undergoing colonoscopic surveillance for colorectal neoplasia.
We conducted a retrospective cohort analysis of 492 patients with colonic IBD for 8 or more years or concomitant primary sclerosing cholangitis, with no history of advanced colorectal neoplasia (high-grade dysplasia or colorectal cancer) or colectomy, undergoing colorectal neoplasia surveillance at a tertiary IBD referral center from 2001 through 2017. Subjects received consistent histopathologic grading of dysplasia. We collected data on time to development of (advanced) colorectal neoplasia or colectomy using Kaplan Meier methods. We identified factors independently associated with (advanced) colorectal neoplasia with multivariable Cox regression analysis.
After 2149 person-years of follow-up, 53 patients (10.8%) received a diagnosis of IND without prior or synchronous low-grade dysplasia (LGD). Compared to patients without dysplasia, patients with IND had a significantly higher risk of advanced colorectal neoplasia (adjusted hazard ratio, 6.85; 95% CI, 1.78-26.4) and colorectal neoplasia (adjusted hazard ratio, 3.25; 95% CI, 1.50-7.05), but not colectomy (P = .78). Compared to IND, LGD was associated with a significantly higher risk of advanced colorectal neoplasia (P = .05). Following a diagnosis of no dysplasia, IND only, or LGD, the incidence rates of advanced colorectal neoplasia were 0.4% per patient-year, 3.1% per patient-year, and 8.4% per patient-year, respectively.
In a retrospective analysis of patients with IBD undergoing colorectal neoplasia surveillance with consistent histopathologic grading of dysplasia, IND was independently associated with a significant increase in risk of advanced colorectal neoplasia. These findings require validation and if confirmed, a reappraisal of the colorectal neoplasia surveillance guidelines.
对于接受结肠镜监测结直肠肿瘤的炎症性肠病(IBD)患者,不定型异型增生(IND)的临床意义知之甚少。
我们对 2001 年至 2017 年在一家三级 IBD 转诊中心接受结直肠肿瘤监测的 492 例 IBD 患者进行了回顾性队列分析,这些患者的结肠 IBD 病史至少 8 年,或同时患有原发性硬化性胆管炎,且无高级结直肠肿瘤(高级别异型增生或结直肠癌)或结肠切除术病史。受试者接受了一致的组织病理学异型增生分级。我们使用 Kaplan-Meier 方法收集了发展为(高级)结直肠肿瘤或结肠切除术的数据。我们使用多变量 Cox 回归分析确定了与(高级)结直肠肿瘤相关的独立因素。
在 2149 人年的随访后,53 例患者(10.8%)在没有先前或同时存在低级别异型增生(LGD)的情况下被诊断为 IND。与无异型增生的患者相比,IND 患者发生高级结直肠肿瘤的风险显著升高(调整后的危险比,6.85;95%可信区间,1.78-26.4)和结直肠肿瘤(调整后的危险比,3.25;95%可信区间,1.50-7.05),但不包括结肠切除术(P =.78)。与 IND 相比,LGD 与高级结直肠肿瘤的风险显著升高相关(P =.05)。在没有异型增生、仅 IND 或 LGD 的诊断后,高级结直肠肿瘤的发生率分别为 0.4%/患者年、3.1%/患者年和 8.4%/患者年。
在对接受结直肠肿瘤监测的 IBD 患者进行回顾性分析时,采用一致的组织病理学异型增生分级,IND 与高级结直肠肿瘤风险显著增加独立相关。这些发现需要验证,如果得到证实,需要重新评估结直肠肿瘤监测指南。