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
WhiteCaramel完成签到 ,获得积分10
1秒前
大猪完成签到 ,获得积分10
1秒前
万事无忧完成签到,获得积分10
2秒前
xdnp2002完成签到 ,获得积分10
4秒前
4秒前
完美麦片完成签到,获得积分10
4秒前
78888完成签到 ,获得积分10
5秒前
零玖完成签到 ,获得积分10
5秒前
支寄灵完成签到,获得积分10
7秒前
小满完成签到 ,获得积分20
7秒前
啊啊啊完成签到 ,获得积分10
7秒前
九九乘法表完成签到,获得积分10
7秒前
luckweb发布了新的文献求助10
7秒前
江海小舟完成签到,获得积分10
9秒前
等待念之完成签到,获得积分10
9秒前
9秒前
10秒前
你好完成签到,获得积分10
11秒前
skyangar完成签到,获得积分10
12秒前
明子完成签到 ,获得积分10
12秒前
Uncanny完成签到,获得积分10
12秒前
贺光萌完成签到 ,获得积分10
12秒前
领导范儿应助哈哈哈采纳,获得10
14秒前
15秒前
小果完成签到 ,获得积分10
15秒前
tiger完成签到,获得积分10
16秒前
沉静冬易完成签到,获得积分10
17秒前
大个应助曾无忧采纳,获得10
17秒前
蜡笔小z完成签到 ,获得积分10
19秒前
方墨发布了新的文献求助30
20秒前
蜗牛fei完成签到,获得积分10
21秒前
叶若相怜完成签到,获得积分10
21秒前
小九完成签到,获得积分10
21秒前
纯真怜梦完成签到,获得积分20
22秒前
AmyHu完成签到,获得积分10
23秒前
李李完成签到,获得积分10
24秒前
tianshanfeihe完成签到 ,获得积分10
25秒前
26秒前
颜凡桃完成签到,获得积分10
27秒前
哈哈哈完成签到,获得积分10
27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
AnnualResearch andConsultation Report of Panorama survey and Investment strategy onChinaIndustry 1000
卤化钙钛矿人工突触的研究 1000
Engineering for calcareous sediments : proceedings of the International Conference on Calcareous Sediments, Perth 15-18 March 1988 / edited by R.J. Jewell, D.C. Andrews 1000
Continuing Syntax 1000
Signals, Systems, and Signal Processing 610
2026 Hospital Accreditation Standards 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 6262843
求助须知:如何正确求助?哪些是违规求助? 8084887
关于积分的说明 16891997
捐赠科研通 5333349
什么是DOI,文献DOI怎么找? 2839003
邀请新用户注册赠送积分活动 1816435
关于科研通互助平台的介绍 1670192