Department of Gastroenterology, Centro Hospitalar Universitário São João, Porto, Portugal.
Department of Biomedicine, Unit of Pharmacology and Therapeutics, Faculty of Medicine, University of Porto, Porto, Portugal.
J Crohns Colitis. 2020 Nov 7;14(11):1503-1511. doi: 10.1093/ecco-jcc/jjaa110.
Currently, the main targets of drug therapy for ulcerative colitis [UC] are endoscopic and clinical remission. However, there is active discussion about the additional advantages of including histological remission as a target. Accumulating evidence indicates that microscopic activity persists in endoscopically quiescent UC, that histological changes may lag behind clinical remission after treatment, and that absence of histological activity predicts lower rates of relapse, hospitalization, surgery and subsequent neoplasia. Obtaining useful information from mucosal biopsies in this setting depends on accurate and consistent evaluation of histological features. However, there is no standardization of biopsy procedures, histological sample processing technique or histological scoring systems, and there is no agreement on the definitions of histological remission, response or activity. Accordingly, a consensus expert panel convened by the European Crohn's and Colitis Organisation [ECCO] reviewed the literature and agreed a number of position statements regarding harmonization of UC histopathology. The objective was to provide evidence-based guidance for the standardization and harmonization of procedures, definitions and scoring systems for histology in UC, and to reach expert consensus where possible. We propose the absence of intraepithelial neutrophils, erosion and ulceration as a minimum requirement for the definition of histological remission. For randomized control trials we recommend the use of the Robarts histopathology index [RHI] or the Nancy index [NI]. For observational studies or in clinical practice we recommend the use of the NI. To predict the risk of future neoplasia in UC, cumulative histological scores over time are more useful than single scores.
目前,溃疡性结肠炎[UC]药物治疗的主要目标是内镜和临床缓解。然而,人们正在积极讨论将组织学缓解作为另一个目标的额外优势。越来越多的证据表明,在内镜下静止的 UC 中仍存在微观活动,治疗后组织学变化可能滞后于临床缓解,并且不存在组织学活动可预测较低的复发、住院、手术和随后的肿瘤发生风险。在这种情况下,从黏膜活检中获得有用信息取决于对组织学特征的准确和一致评估。然而,活检程序、组织学样本处理技术或组织学评分系统没有标准化,组织学缓解、反应或活动的定义也没有达成一致。因此,欧洲克罗恩病和结肠炎组织[ECCO]召集的一个共识专家小组审查了文献,并就 UC 组织病理学的协调一致达成了一些立场声明。目的是为 UC 中的组织学标准化和协调一致提供循证指导,尽可能达成专家共识。我们建议将上皮内中性粒细胞、糜烂和溃疡的缺失作为组织学缓解定义的最低要求。对于随机对照试验,我们建议使用罗巴特组织病理学指数[RHI]或南希指数[NI]。对于观察性研究或临床实践,我们建议使用 NI。为了预测 UC 中未来肿瘤的风险,随时间累积的组织学评分比单次评分更有用。