已入深夜,您辛苦了!由于当前在线用户较少,发布求助请尽量完整地填写文献信息,科研通机器人24小时在线,伴您度过漫漫科研夜!祝你早点完成任务,早点休息,好梦!

Real-world comparison of the effectiveness between ustekinumab and vedolizumab in patients with ulcerative colitis exposed to at least one anti-TNF agent

维多利祖马布 乌斯特基努马 溃疡性结肠炎 医学 肿瘤坏死因子α 内科学 胃肠病学 英夫利昔单抗 疾病
作者
Mathurin Fuméry,Mélanie Serrero,Guillaume Bouguen,Aurélien Amiot,Romain Altwegg,Maria Nachury,Lucine Vuitton,Xavier Tréton,Ludovic Caillo,Bruno Pereira,Anthony Buisson
出处
期刊:Journal of Crohn's and Colitis [Oxford University Press]
标识
DOI:10.1093/ecco-jcc/jjae063
摘要

Abstract Background Both vedolizumab and ustekinumab can be considered for the treatment of ulcerative colitis [UC], but head-to-head trials are lacking. Aim We aimed to compare the effectiveness of vedolizumab and ustekinumab after anti-tumour necrosis factor [anti-TNF] failure in UC patients. Patients and Methods In this multicentre study, we included consecutive adult patients with UC, with partial Mayo score >2 and prior anti-TNF exposure, treated with vedolizumab or ustekinumab between January 2019 and August 2022. Comparisons were performed using propensity score analyses [inverse probability of treatment weighting]. Results Among a total of 293 patients included, 151 and 142 received vedolizumab and ustekinumab, respectively. After propensity score analysis, steroid-free clinical remission [SFCR] [partial Mayo score ≤2] was achieved at week 16 in 38.0% and 40.3% of patients treated with vedolizumab and ustekinumab, respectively (adjusted odds ratio [aOR] = 1.11, 95% confidence interval [0.39–3.13], p = 0.85). Rates of SFCR in patients exposed to one, two, and three lines of biologics/small molecules among patients treated with vedolizumab and ustekinumab were respectively 53.3% vs 62.1% [p = 0.52], 44.4% vs 33.8% [p = 0.52], and 2.6% vs 19.1% [p = 0.027]. Endoscopic remission [SFCR and endoscopic Mayo score ≤1] and histological remission [SFCR, endoscopic remission, and Nancy histological index ≤1] at week 16 were achieved in respectively 5.3% vs 17.5% (aOR = 3.77 [1.25–11.36], p = 0.018) and 2.1% vs 11.1% (aOR = 5.85 [1.47–23.30], p = 0.012) in the vedolizumab and ustekinumab groups. No difference regarding the risk of drug discontinuation between the two groups (aHR = 1.03 [0.51–2.08], p = 0.92) was observed. While no factor was identified for vedolizumab, primary failure to at least one biologic/small molecule (OR = 0.31 [0.11–0.82], p = 0.018) was significantly associated with a decreased rate of SFCR among patients treated with ustekinumab. Conclusion While no difference in terms of short-term clinical remission was observed, ustekinumab appears to be more effective than vedolizumab in inducing endoscopic and histological remission at week 16 after failure of anti-TNFs in UC.

科研通智能强力驱动
Strongly Powered by AbleSci AI
科研通是完全免费的文献互助平台,具备全网最快的应助速度,最高的求助完成率。 对每一个文献求助,科研通都将尽心尽力,给求助人一个满意的交代。
实时播报
刚刚
1秒前
科目三应助赖床的羊采纳,获得10
2秒前
香蕉觅云应助Cici采纳,获得10
3秒前
抹茶麻薯发布了新的文献求助10
4秒前
林子鸿完成签到 ,获得积分10
5秒前
6秒前
铲子发布了新的文献求助10
6秒前
Vicki完成签到,获得积分0
7秒前
7秒前
杨科完成签到,获得积分10
8秒前
米花完成签到 ,获得积分10
9秒前
LL发布了新的文献求助10
9秒前
10秒前
17秒前
虚无完成签到,获得积分10
17秒前
月亮与六便士完成签到,获得积分10
20秒前
21秒前
辛勤依凝发布了新的文献求助10
21秒前
25秒前
25秒前
JT发布了新的文献求助10
26秒前
求文献完成签到,获得积分10
26秒前
28秒前
NexusExplorer应助拟闲采纳,获得10
31秒前
铲子完成签到,获得积分10
37秒前
38秒前
徐继军完成签到 ,获得积分10
38秒前
saber完成签到 ,获得积分10
39秒前
调皮的笑阳完成签到 ,获得积分10
39秒前
可爱的函函应助辛勤依凝采纳,获得10
40秒前
云落完成签到 ,获得积分10
41秒前
43秒前
46秒前
OOK发布了新的文献求助10
46秒前
个性的南珍完成签到 ,获得积分10
51秒前
赖床的羊发布了新的文献求助10
51秒前
童严柯发布了新的文献求助10
52秒前
抹茶麻薯发布了新的文献求助10
53秒前
能干的阿拉蕾完成签到 ,获得积分10
54秒前
高分求助中
(应助此贴封号)【重要!!请各用户(尤其是新用户)详细阅读】【科研通的精品贴汇总】 10000
HANDBOOK OF CHEMISTRY AND PHYSICS 106th edition 1000
ASPEN Adult Nutrition Support Core Curriculum, Fourth Edition 1000
AnnualResearch andConsultation Report of Panorama survey and Investment strategy onChinaIndustry 1000
Continuing Syntax 1000
Signals, Systems, and Signal Processing 610
Decentring Leadership 500
热门求助领域 (近24小时)
化学 材料科学 医学 生物 纳米技术 工程类 有机化学 化学工程 生物化学 计算机科学 物理 内科学 复合材料 催化作用 物理化学 光电子学 电极 细胞生物学 基因 无机化学
热门帖子
关注 科研通微信公众号,转发送积分 6277260
求助须知:如何正确求助?哪些是违规求助? 8096857
关于积分的说明 16926547
捐赠科研通 5346365
什么是DOI,文献DOI怎么找? 2842392
邀请新用户注册赠送积分活动 1819644
关于科研通互助平台的介绍 1676797