使用MM-SES-CD内镜改善阈值可增强阿达木单抗与安慰剂之间的效应大小区分:EXTEND试验的事后分析。

Emily C L Wong, Parambir S Dulai, John K Marshall, Stephen Laroux, Vipul Jairath, Walter Reinisch, Neeraj Narula
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摘要

简介:修正的 SES-CD 乘数(MM-SES-CD)通过对原始 SES-CD 中的参数进行不同的加权,完善了对内镜克罗恩病(CD)严重程度的评估。方法的阈值:这项EXTEND试验的事后分析比较了各种SES-CD和MM-SES-CD对阿达木单抗或安慰剂治疗的克罗恩病患者ER和内镜反应的定义。该研究纳入了患有中度-重度CD且基线MM-SES-CD评分≥22.5分的患者。ER的主要结果定义为MM-SES-CD结果:在100名参与者(占EXTEND人群的77.5%)中,51人接受了阿达木单抗治疗,49人接受了安慰剂治疗。第12周时,62%的患者MM-SES-CD较基线下降≥20%,而SES-CD下降≥50%的患者为39%。第52周时,56.9%的阿达木单抗治疗参与者达到了MM-SES-CD结论:MM-SES-CD定义提高了治疗与安慰剂之间的区分度,并为第52周ER提供了更高的预测准确性。使用它可以提高试验效率,更好地预测长期疾病结果。
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Use of MM-SES-CD Endoscopic Improvement Thresholds Enhances Effect Size Differentiation between Adalimumab vs. Placebo: A Post-hoc Analysis of the EXTEND Trial.

Introduction: The Modified Multiplier of the SES-CD (MM-SES-CD) refines the assessment of endoscopic Crohn's Disease (CD) severity by differentially weighting parameters in the original SES-CD. A threshold of <22.5 for MM-SES-CD suggests endoscopic remission and correlates with a low risk of long-term disease progression. This study examines whether MM-SES-CD-defined endoscopic remission (ER) and response criteria are more sensitive to treatment effects compared to conventional SES-CD definitions.

Methods: This post-hoc analysis of the EXTEND trial compared various SES-CD and MM-SES-CD definitions of ER and endoscopic response in CD patients treated with adalimumab or placebo. The study included participants with moderate-severe CD and a baseline MM-SES-CD score ≥22.5. The primary outcome of ER, defined as MM-SES-CD <22.5, was evaluated at weeks 12 and 52. AUC analyses compared thresholds for predicting week 52 ER.

Results: Of the 100 participants (77.5% of the EXTEND population), 51 received adalimumab and 49 placebo. At week 12, 62% achieved MM-SES-CD ≥20% reduction from baseline, compared to 39% with SES-CD ≥50% reduction. At week 52, 56.9% of adalimumab-treated participants achieved MM-SES-CD <22.5, compared to 10.2% in the placebo group. MM-SES-CD ≥20% reduction at week 12 better predicted week 52 ER than SES-CD ≥50% reduction (AUC: 0.73 vs. 0.62, p=0.002).

Conclusion: MM-SES-CD definitions improved discrimination between treatment and placebo and offered superior predictive accuracy for week 52 ER. Its use may enhance trial efficiency and better predict long-term disease outcomes.

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