Bokemeyer Bernd, Plachta-Danielzik Sandra, Gilman Elena, di Giuseppe Romina, Deppe Herbert, Mohl Wolfgang, Teich Niels, Hoffstadt Martin, Schweitzer Axel, von der Ohe Manfred, Gauss Annika, Atreya Raja, Krause Thomas, Blumenstein Irina, Hartmann Petra, Schreiber Stefan
Interdisciplinary Crohn Colitis Centre Minden, Germany.
Clinic of General Internal Medicine I, University Hospital Schleswig-Holstein, Campus Kiel, Germany.
J Crohns Colitis. 2025 Apr 4;19(4). doi: 10.1093/ecco-jcc/jjaf051.
The prospective RUN-CD registry investigates the effectiveness of ustekinumab (UST) and other biologics in Crohn's disease (CD) across Germany. Based on data from the registry, this study presents the maintenance phase results of a 12-month real-world-evidence (RWE) comparison of CD patients initiating new biologic therapies with UST or anti-TNF.
After excluding patients using biologics other than UST and anti-TNF and those with missing outcomes, the final sample consisted of 618 CD patients. Clinical remission (CR), defined as a Harvey-Bradshaw Index (HBI) ≤4, was the prespecified endpoint at 12 months. Switching to another biologic therapy was considered an outcome failure. Propensity score adjustment was used to reduce the effect of confounders.
The study included 343 CD patients treated with UST and 264 treated with anti-TNF. Over 12 months, the frequency of therapy switches was significantly higher for infliximab (28%) compared with UST (17%) and adalimumab (17%) (P =.045). There was no significant difference in CR rates at 12 months between the UST and anti-TNF groups (65.8% vs 60.0%, P =.262). However, in week-16 responders, CR rates at 12 months were significantly higher with UST (77.6%) versus anti-TNF (65.4%) (P =.041). The change in EQ-VAS (QoL) scores between UST and anti-TNF showed a 5.1-point difference favoring UST (P =.002).
In this 12-month RWE comparison, overall CR rates were similar between UST and anti-TNF. However, among week-16 responders, CR rates were significantly higher with UST. Additionally, UST was associated with a significantly greater improvement in QoL compared with anti-TNF.
前瞻性RUN-CD注册研究在德国调查了优特克单抗(UST)和其他生物制剂对克罗恩病(CD)的疗效。基于该注册研究的数据,本研究展示了开始使用UST或抗TNF进行新生物治疗的CD患者12个月真实世界证据(RWE)比较的维持阶段结果。
在排除使用UST和抗TNF以外生物制剂的患者以及结局缺失的患者后,最终样本包括618例CD患者。临床缓解(CR)定义为哈维-布拉德肖指数(HBI)≤4,是12个月时预先设定的终点。改用另一种生物治疗被视为结局失败。采用倾向评分调整以减少混杂因素的影响。
该研究纳入了343例接受UST治疗的CD患者和264例接受抗TNF治疗的患者。在12个月期间,英夫利昔单抗的治疗转换频率(28%)显著高于UST(17%)和阿达木单抗(17%)(P = 0.045)。UST组和抗TNF组在12个月时的CR率无显著差异(65.8%对60.0%,P = 0.262)。然而,在第16周有反应者中,UST组12个月时的CR率(77.6%)显著高于抗TNF组(65.4%)(P = 0.041)。UST和抗TNF之间的EQ-VAS(生活质量)评分变化显示,UST有5.1分的优势(P = 0.002)。
在这项12个月的RWE比较中,UST和抗TNF的总体CR率相似。然而,在第16周有反应者中,UST的CR率显著更高。此外,与抗TNF相比,UST与生活质量的显著更大改善相关。