Departement of Medical Science and Public Health, Gastroenterology Unit, University of Cagliari, Cagliari, Italy.
Gastroenterology Unit, Azienda Ospedaliero-Universitaria (AOU) di Cagliari, Cagliari, Italy.
Am J Gastroenterol. 2022 Aug 1;117(8):1279-1287. doi: 10.14309/ajg.0000000000001773. Epub 2022 Apr 13.
The use of ustekinumab and vedolizumab as second-line therapies in patients with Crohn's disease (CD) in which tumour necrosis factor alpha inhibitors (TNFi) failed is still debated. The aim of this study was to compare, in a large multicenter observational retrospective cohort, the effectiveness of ustekinumab and vedolizumab as second-line therapies, as assessed by clinical and objective outcomes including endoscopy and gastrointestinal imaging.
Clinical response, remission, and steroid-free remission at weeks 26 and 52 were evaluated in a retrospective propensity score-weighted and propensity score-matched cohort of patients in which TNFi failed. Objective response and remission were evaluated by 1 or more techniques among endoscopy, magnetic resonance/computed tomography enteroclysis, and small bowel ultrasound.
A total of 470 patients with CD (239 treated with ustekinumab and 231 treated with vedolizumab) were included in the study. At week 26, clinical outcomes were similar between the 2 groups. At week 52, clinical remission (ustekinumab 42.5% vs vedolizumab 55.5%, P = 0.01) and steroid-free remission (ustekinumab 40.6% vs vedolizumab 51.1%, P = 0.038) rates were significantly higher in vedolizumab-treated patients. Three hundred two patients (hundred thirty-five treated with ustekinumab and hundred sixty-seven treated with vedolizumab) had an objective evaluation of disease activity at baseline and week 52. At week 52, objective response and remission rates were similar between the 2 groups. Clinical response at week 26 predicted steroid-free remission at week 52 in both ustekinumab-treated and vedolizumab-treated patients. Safety profiles were similar between the 2 groups.
In patients with CD in which TNFi failed, both ustekinumab and vedolizumab showed similar clinical effectiveness after 26 weeks of treatment. At 1 year, vedolizumab was associated with a higher rate of clinical remission when compared with ustekinumab. However, no difference was observed between the 2 groups when objective outcomes were investigated at this time point.
在肿瘤坏死因子-α抑制剂(TNFi)治疗失败的克罗恩病(CD)患者中,使用乌司奴单抗和维得利珠单抗作为二线治疗仍存在争议。本研究的目的是在一项大型多中心回顾性队列研究中,比较乌司奴单抗和维得利珠单抗作为二线治疗的有效性,通过临床和客观结局(包括内镜和胃肠影像学)进行评估。
在 TNFi 治疗失败的患者回顾性倾向评分加权和倾向评分匹配队列中,评估第 26 周和第 52 周的临床缓解、缓解和无激素缓解。通过内镜、磁共振/计算机断层肠造影术和小肠超声等 1 种或多种技术评估客观缓解和缓解。
共纳入 470 例 CD 患者(乌司奴单抗治疗 239 例,维得利珠单抗治疗 231 例)。第 26 周时,两组的临床结局相似。第 52 周时,维得利珠单抗治疗组的临床缓解率(乌司奴单抗 42.5%比维得利珠单抗 55.5%,P=0.01)和无激素缓解率(乌司奴单抗 40.6%比维得利珠单抗 51.1%,P=0.038)显著更高。302 例患者(乌司奴单抗治疗 135 例,维得利珠单抗治疗 167 例)在基线和第 52 周时进行了疾病活动的客观评估。第 52 周时,两组的客观缓解率和缓解率相似。第 26 周的临床缓解预测了第 52 周的无激素缓解,无论是乌司奴单抗治疗还是维得利珠单抗治疗的患者均是如此。两组的安全性特征相似。
在 TNFi 治疗失败的 CD 患者中,乌司奴单抗和维得利珠单抗在治疗 26 周后均显示出相似的临床疗效。在 1 年时,与乌司奴单抗相比,维得利珠单抗与更高的临床缓解率相关。然而,在这个时间点,当调查客观结局时,两组之间没有观察到差异。