Bokemeyer Bernd, Plachta-Danielzik Sandra, Gilman Elena, Howaldt Stefanie, Mohl Wolfgang, Efken Philipp, Ehehalt Robert, Kahl Matthias, Krause Thomas, Trentmann Leo, Lügering Andreas, Schnoy Elisabeth, Jochum Christoph, Hartmann Petra, Schreiber Stefan
Interdisciplinary Crohn Colitis Centre Minden, Minden, Germany.
Clinic of General Internal Medicine I, University Hospital Schleswig-Holstein, Kiel, Germany.
J Crohns Colitis. 2025 May 8;19(5). doi: 10.1093/ecco-jcc/jjaf052.
Real-world evidence studies of ustekinumab (UST) in ulcerative colitis (UC) are needed because randomized controlled trials do not represent unselected patient populations in everyday clinical practice. Patients with UC were recruited when starting biologic therapy for the first time or switching to a new biologic therapy. This study assessed the effectiveness of maintenance therapy with UST in comparison to anti-TNF or vedolizumab (VDZ) at 12 months.
Between 2020 and 2022, 507 UC patients starting biologic therapy for the first time or switching to a new biologic therapy were enrolled at 34 inflammatory bowel disease (IBD)-specialized centers in Germany. After excluding patients receiving other biologics or small molecules, as well as those with stomas or missing outcomes, the final sample consisted of 476 patients. The outcomes were clinical response, clinical remission (CR), and steroid-free remission. Propensity score (PS) adjustment with inverse probability of treatment weighting was used to reduce the effect of confounding due to physician selection of therapy.
A total of 476 patients with UC were included in the analysis (UST: 147, anti-TNF: 168, VDZ: 161). Treatment persistence over 12 months differed significantly (P < .001) between UST (93.9%), VDZ (87.0%), and anti-TNF (75.0%). The PS-weighted effectiveness of UST in the mITT analysis at month 12 was not significantly different from anti-TNF or VDZ (CR: UST 26.9%, anti-TNF 34.7%, VDZ 40.9%; P = .063).
In the prospective RUN-UC study with PS-weighted groups, UST showed higher treatment persistence but no significant difference in maintenance effectiveness compared to anti-TNF or VDZ in UC.
需要开展关于乌司奴单抗(UST)治疗溃疡性结肠炎(UC)的真实世界证据研究,因为随机对照试验无法代表日常临床实践中未经筛选的患者群体。UC患者在首次开始生物治疗或换用新的生物治疗时被纳入研究。本研究评估了12个月时UST维持治疗与抗TNF或维多珠单抗(VDZ)相比的有效性。
2020年至2022年期间,德国34个炎症性肠病(IBD)专科中心纳入了507例首次开始生物治疗或换用新生物治疗的UC患者。排除接受其他生物制剂或小分子药物治疗的患者,以及有造口或结局缺失的患者后,最终样本包括476例患者。结局指标为临床缓解、临床应答(CR)和无激素缓解。采用倾向评分(PS)调整及治疗权重逆概率法来降低医生选择治疗导致的混杂效应。
分析共纳入476例UC患者(UST组:147例,抗TNF组:168例,VDZ组:161例)。UST组(93.9%)、VDZ组(87.0%)和抗TNF组(75.0%)的12个月治疗持续率差异有统计学意义(P<0.001)。在第12个月的mITT分析中,UST经PS加权后的有效性与抗TNF或VDZ相比无显著差异(CR:UST组26.9%,抗TNF组34.7%,VDZ组40.9%;P=0.063)。
在前瞻性的RUN-UC研究的PS加权组中,UST在UC中的治疗持续率较高,但与抗TNF或VDZ相比,维持治疗有效性无显著差异。