Combination therapy is not associated with improved rates of clinical or endoscopic remission in patients with inflammatory bowel disease treated with ustekinumab or vedolizumab: a retrospective study.

IF 2.1 Q3 GASTROENTEROLOGY & HEPATOLOGY Annals of Gastroenterology Pub Date : 2023-07-01 Epub Date: 2023-05-29 DOI:10.20524/aog.2023.0808
Angus W Jeffrey, Sherman Picardo, Shankar Menon, Kenji So, Kannan Venugopal
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引用次数: 1

Abstract

Background: Management of inflammatory bowel disease (IBD) involves biological agents, often in combination with thiopurines or methotrexate. The aim of our study was to compare clinical and endoscopic outcomes in IBD patients treated with vedolizumab or ustekinumab, as monotherapy or in combination with thiopurines or methotrexate.

Methods: We conducted a retrospective cohort study of all patients aged ≥18 years with a diagnosis of ulcerative colitis or Crohn's disease, commenced on vedolizumab or ustekinumab between October 2015 and March 2022. Primary outcome was clinical remission or response calculated by partial Mayo score (remission: <3; response: improvement >1) for ulcerative colitis or Harvey-Bradshaw index (<5, >2 respectively) for Crohn's disease over 1 year. Secondary endpoints were treatment failure, relapse, endoscopic remission at 1 year. Statistical analysis was done using 2-sample Student's t and chi-square tests.

Results: A total of 159 IBD patients were included in the study, 85 (53%) on vedolizumab and 74 (47%) on ustekinumab. For those on vedolizumab, 61 (72%) patients had ulcerative colitis, and 24 (28%) has Crohn's disease. All patients on ustekinumab had Crohn's disease. Mean disease duration in was 9.4 and 13.5 years respectively. There was no difference in clinical response or remission for vedolizumab or ustekinumab monotherapy compared to combination therapy at 1 year. There was also no difference in treatment failure, relapse or endoscopic remission.

Conclusion: Combining vedolizumab or ustekinumab with an immunomodulator is not superior to monotherapy in terms of clinical response or endoscopic remission up to 1 year in IBD.

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联合治疗与使用ustekinumab或vedolizumab治疗的炎症性肠病患者的临床或内镜缓解率提高无关:一项回顾性研究。
背景:炎症性肠病(IBD)的治疗涉及生物制剂,通常与硫嘌呤或甲氨蝶呤联合使用。我们研究的目的是比较韦多珠单抗或ustekinumab单药治疗或与硫嘌呤或甲氨蝶呤联合治疗IBD患者的临床和内镜结果。方法:我们对所有年龄≥18岁、诊断为溃疡性结肠炎或克罗恩病的患者进行了一项回顾性队列研究,该研究于2015年10月至2022年3月期间开始使用维多利珠单抗或ustekinumab。主要结果是通过溃疡性结肠炎的部分Mayo评分(缓解:1)或克罗恩病的Harvey-Bradshaw指数(分别为2)计算1年以上的临床缓解或反应。次要终点为治疗失败、复发、1年时内镜缓解。使用两个样本的Student t和卡方检验进行统计分析。结果:共有159名IBD患者被纳入该研究,其中85名(53%)接受韦多利珠单抗治疗,74名(47%)接受ustekinumab治疗。在服用韦多利珠单抗的患者中,61名(72%)患者患有溃疡性结肠炎,24名(28%)患者患有克罗恩病。所有使用ustekinumab的患者都患有克罗恩病。年平均病程分别为9.4年和13.5年。与1年时的联合治疗相比,维多利珠单抗或ustekinumab单药治疗的临床反应或缓解没有差异。在治疗失败、复发或内镜缓解方面也没有差异。结论:就IBD的临床反应或内镜下长达1年的缓解而言,韦多利珠单抗或ustekinumab与免疫调节剂联合治疗并不优于单一疗法。
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来源期刊
Annals of Gastroenterology
Annals of Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
4.30
自引率
0.00%
发文量
58
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