Meade Susanna, Routledge Emma, Sharma Esha, Honap Sailish, Zeki Sebastian, Ray Shuvra, Anderson Simon H C, Sanderson Jeremy, Mawdsley Joel, Irving Peter M, Samaan Mark A
IBD Centre, Department of Gastroenterology, Guy's and St Thomas' Hospitals NHS Trust, London, UK.
Pharmacy Department, Guy's and Saint Thomas' Hospitals NHS Trust, London, UK.
Frontline Gastroenterol. 2022 Dec 7;14(4):312-318. doi: 10.1136/flgastro-2022-102309. eCollection 2023.
The second iteration of the Selecting Therapeutic Targets in Inflammatory Bowel Disease (STRIDE-II) initiative recommends use of the Simple Endoscopic Score for Crohn's disease (SES-CD) as a treatment target for patients with CD. We aimed to assess whether the STRIDE-II endoscopic endpoints are achievable and whether the degree of mucosal healing (MH) affects long-term outcomes.
DESIGN/METHOD: We performed a retrospective observational study between 2015 and 2022. Patients with CD who had baseline and follow-up SES-CD scores after biological therapy initiation were included. The primary outcome was treatment failure, defined as the need for: (1) change of biological therapy for active disease (2) corticosteroid use (3) CD-related hospitalisation or (4) surgery. We compared rates of treatment failure with the degree of MH achieved. Patients were followed up until treatment failure or study end (August 2022).
50 patients were included and followed up for median 39.9 (34.6-48.6) months. Baseline characteristics: 62% male, median age 36.4 (27.8-43.9) years, disease distribution (L1: 4, L2: 11, L3: 35, perianal: 18). The proportion of patients achieving STRIDE-II end-points were: SES-CD2-25 (50%) and >50% reduction in SES-CD-35 (70%). Failure to achieve SES-CD2 (HR 11.62; 95% CI 3.33 to 40.56, p=0.003) or >50% improvement in SES-CD (HR 30.30; 95% CI 6.93 to 132.40, p<0.0001) predicted treatment failure.
Use of SES-CD is feasible in real-world clinical practice. Achieving an SES-CD2 or a greater than 50% reduction, as set out by STRIDE-II, is associated with reduced rates of overall treatment failure including CD-related surgery.
炎症性肠病治疗靶点选择(STRIDE-II)计划的第二次迭代建议将克罗恩病简易内镜评分(SES-CD)作为克罗恩病(CD)患者的治疗目标。我们旨在评估STRIDE-II内镜终点是否可实现,以及黏膜愈合(MH)程度是否会影响长期预后。
设计/方法:我们在2015年至2022年期间进行了一项回顾性观察研究。纳入在开始生物治疗后有基线和随访SES-CD评分的CD患者。主要结局是治疗失败,定义为需要:(1)因活动性疾病改变生物治疗;(2)使用皮质类固醇;(3)因CD住院或(4)手术。我们比较了治疗失败率与达到的MH程度。对患者进行随访,直至治疗失败或研究结束(2022年8月)。
纳入50例患者,中位随访39.9(34.6 - 48.6)个月。基线特征:男性占62%,中位年龄36.4(27.8 - 43.9)岁,疾病分布(L1:4例,L2:11例,L3:35例,肛周:18例)。达到STRIDE-II终点的患者比例为:SES-CD2 - 25(50%)和SES-CD降低>50%(70%)。未达到SES-CD2(风险比11.62;95%置信区间3.33至40.56,p = 0.003)或SES-CD改善>50%(风险比30.30;95%置信区间6.93至132.40,p < 0.0001)可预测治疗失败。
在实际临床实践中使用SES-CD是可行的。达到STRIDE-II规定的SES-CD2或降低大于50%与包括CD相关手术在内的总体治疗失败率降低相关。