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生物制剂初治克罗恩病中英夫利昔单抗与乌司奴单抗的疗效和起效速度比较。

Comparative Efficacy and Rapidity of Action for Infliximab vs Ustekinumab in Biologic Naïve Crohn's Disease.

机构信息

Division of Gastroenterology, Department of Medicine, Farncombe Family Digestive Health Research Institute, McMaster University, Hamilton, Ontario, Canada.

Division of Gastroenterology, Department of Medicine, Farncombe Family Digestive Health Research Institute, McMaster University, Hamilton, Ontario, Canada.

出版信息

Clin Gastroenterol Hepatol. 2022 Jul;20(7):1579-1587.e2. doi: 10.1016/j.cgh.2021.04.006. Epub 2021 Apr 7.

Abstract

BACKGROUND & AIMS: Comparative effectiveness has become increasingly important to help position therapies for inflammatory bowel disease. We compared the efficacy and rapidity of onset of action of infliximab vs ustekinumab induction therapy for moderate to severe biologic-naïve Crohn's disease (CD) using patient-level data from randomized controlled trials.

METHODS

This was a post hoc analysis of 2 large CD clinical trial programs that included data on 420 biologic-naïve CD patients. Differences in proportions of patients achieving week 6 clinical remission, clinical response, and normalization of calprotectin were compared. Multivariate logistic regression was used to adjust for confounders. Sensitivity analysis was conducted using propensity scores to create a cohort of matched participants with similar distribution of baseline covariates.

RESULTS

At week 6, a comparable number of patients achieved clinical remission with infliximab compared with patients treated with ustekinumab (44.9% vs 37.9%; adjusted odds ratio [aOR], 1.22; 95% CI, 0.79-1.89). Similarly, at week 6 the clinical response rates were not significantly different (58.4% infliximab vs 54.9% ustekinumab; aOR, 1.25; 95% CI, 0.82-1.90). No significant difference was observed between treatment groups for achieving a week 6 fecal calprotectin level less than 250 mcg/L in those with increased values at baseline (42.3% infliximab vs 34.7% ustekinumab; aOR, 1.34; 95% CI, 0.79-2.28). Similar results were seen for all analyses performed within the propensity matched cohort.

CONCLUSIONS

Based on this post hoc analysis, infliximab and ustekinumab appear to have similar efficacy and speed of onset in patients with CD who are biologic-naïve.

摘要

背景与目的

为帮助定位炎症性肠病的治疗方法,比较疗效变得越来越重要。我们使用来自随机对照试验的患者水平数据,比较了英夫利昔单抗与乌司奴单抗诱导治疗中重度生物初治克罗恩病(CD)的疗效和起效速度。

方法

这是两项大型 CD 临床试验计划的事后分析,包括 420 名生物初治 CD 患者的数据。比较了第 6 周达到临床缓解、临床应答和钙卫蛋白正常化的患者比例的差异。使用多变量逻辑回归调整混杂因素。使用倾向评分进行敏感性分析,创建一个具有相似基线协变量分布的匹配参与者队列。

结果

第 6 周时,接受英夫利昔单抗治疗的患者达到临床缓解的比例与接受乌司奴单抗治疗的患者相似(44.9% vs 37.9%;调整后的优势比[aOR],1.22;95%置信区间[CI],0.79-1.89)。同样,第 6 周时临床应答率也没有显著差异(58.4%英夫利昔单抗 vs 54.9%乌司奴单抗;aOR,1.25;95%CI,0.82-1.90)。在基线值升高的患者中,第 6 周粪便钙卫蛋白水平低于 250 mcg/L 的患者中,两组之间也没有观察到治疗组之间有显著差异(42.3%英夫利昔单抗 vs 34.7%乌司奴单抗;aOR,1.34;95%CI,0.79-2.28)。在倾向匹配队列中进行的所有分析中都观察到了类似的结果。

结论

基于这项事后分析,英夫利昔单抗和乌司奴单抗在生物初治 CD 患者中的疗效和起效速度似乎相似。

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