溃疡性结肠炎临床试验中组织病理学整合的国际共识标准化

An International Consensus to Standardize Integration of Histopathology in Ulcerative Colitis Clinical Trials.

机构信息

Division of Gastroenterology and Hepatology, Departments of Medicine and Community Health Sciences, Cumming School of Medicine, University of Calgary, Calgary, Alberta, Canada; Alimentiv Inc (formerly Robarts Clinical Trials, Inc), London, Ontario, Canada.

Department of Medicine, Division of Gastroenterology, Western University, London, Ontario, Canada.

出版信息

Gastroenterology. 2021 Jun;160(7):2291-2302. doi: 10.1053/j.gastro.2021.02.035. Epub 2021 Feb 19.

Abstract

BACKGROUND & AIMS: Histopathology is an emerging treatment target in ulcerative colitis (UC) clinical trials. Our aim was to provide guidance on standardizing biopsy collection protocols, identifying optimal evaluative indices, and defining thresholds for histologic response and remission after treatment.

METHODS

An international, interdisciplinary expert panel of 19 gastroenterologists and gastrointestinal pathologists was assembled. A modified RAND/University of California, Los Angeles appropriateness methodology was used to address relevant issues. A total of 138 statements were derived from a systematic review of the literature and expert opinion. Each statement was anonymously rated as appropriate, uncertain, or inappropriate using a 9-point scale. Survey results were reviewed and discussed before a second round of voting.

RESULTS

Histologic measurements collected using a uniform biopsy strategy are important for assessing disease activity and determining therapeutic efficacy in UC clinical trials. Multiple biopsy strategies were deemed acceptable, including segmental biopsies collected according to the endoscopic appearance. Biopsies should be scored for architectural change, lamina propria chronic inflammation, basal plasmacytosis, lamina propria and epithelial neutrophils, epithelial damage, and erosions/ulcerations. The Geboes score, Robarts Histopathology Index, and Nancy Index were considered appropriate for assessing histologic activity; use of the modified Riley score and Harpaz Index were uncertain. Histologic activity at baseline should be required for enrollment, recognizing this carries operational implications. Achievement of histologic improvement or remission was considered an appropriate and realistic therapeutic target. Current histologic indices require validation for pediatric populations.

CONCLUSIONS

These recommendations provide a framework for standardized implementation of histopathology in UC trials. Additional work is required to address operational considerations and areas of uncertainty.

摘要

背景与目的

组织病理学是溃疡性结肠炎(UC)临床试验中的一个新兴治疗靶点。我们的目的是提供关于标准化活检采集方案、确定最佳评估指标以及定义治疗后组织学反应和缓解阈值的指导。

方法

召集了一个由 19 名胃肠病学家和胃肠病理学家组成的国际跨学科专家小组。采用改良的 RAND/加利福尼亚大学洛杉矶分校适宜性方法来解决相关问题。从文献系统评价和专家意见中得出了总共 138 条陈述。使用 9 分制对每个陈述进行匿名评分,分为合适、不确定或不合适。在第二轮投票之前,审查和讨论调查结果。

结果

使用统一的活检策略收集的组织学测量对于评估 UC 临床试验中的疾病活动和确定治疗效果很重要。多种活检策略被认为是可以接受的,包括根据内镜表现采集的节段性活检。活检应针对结构改变、固有层慢性炎症、基底浆细胞增多、固有层和上皮中性粒细胞、上皮损伤以及糜烂/溃疡进行评分。Geboes 评分、Robarts 组织病理学指数和 Nancy 指数被认为适用于评估组织学活性;使用改良的 Riley 评分和 Harpaz 指数是不确定的。基线时的组织学活性应作为入组的要求,这需要考虑操作方面的影响。实现组织学改善或缓解被认为是一个合适且现实的治疗目标。目前的组织学指数需要针对儿科人群进行验证。

结论

这些建议为在 UC 试验中标准化实施组织病理学提供了一个框架。需要进一步的工作来解决操作方面的考虑因素和不确定的领域。

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