Shehab Mohammad, Alrashed Fatema, Alsayegh Abdulwahab, Aldallal Usama, Ma Christopher, Narula Neeraj, Jairath Vipul, Singh Siddharth, Bessissow Talat
Division of Gastroenterology, Department of Internal Medicine, Mubarak Alkabeer University Hospital, Kuwait; Department of Pharmacy Practice, Faculty of Pharmacy, Kuwait University, Jabriya, Kuwait.
Department of Pharmacy Practice, Faculty of Pharmacy, Kuwait University, Jabriya, Kuwait.
Clin Gastroenterol Hepatol. 2025 Feb;23(2):250-262. doi: 10.1016/j.cgh.2024.07.033. Epub 2024 Sep 5.
BACKGROUND & AIMS: Treatment options for moderate to severe ulcerative colitis (UC) are increasing rapidly, but the lack of comparative efficacy trials makes treatment choices a clinical challenge. This network-meta-analysis aimed to compare the relative efficacy of biologics and small molecules in achieving remission in patients with moderate to severe UC.
The literature was searched up to May 2024. Phase 3 placebo or active comparator randomized controlled trials were included. The primary outcome was induction and maintenance of endoscopic improvement (Mayo Endoscopic Score [MES] ≤1). Secondary outcomes were the induction and maintenance of clinical remission, endoscopic (MES = 0) and histological remission. A sub-analysis was performed based on the randomized controlled trial design and previous exposure to biologic therapy.
We identified 36 studies that met our inclusion criteria, with 14,270 patients with UC. Upadacitinib ranked highest in inducing clinical remission (99.6%), and endoscopic improvement (99.2%), followed by risankizumab (91.4%) and (82.3%), respectively. In maintenance of endoscopic improvement, upadacitinib ranked first (98.6%) followed by filgotinib 200 mg (79.2%). Risankizumab ranked first in the induction of histological remission (89.4%), followed by guselkumab (88.3%). Upadacitinib ranked first (93.1%) in maintaining histological remission, followed by guselkumab (89.5%).
Upadacitinib appears to be superior to other therapies in achieving clinical remission, endoscopic improvement and remission, and histological remission. Furthermore, novel biologics such as risankizumab and guselkumab ranked high in achieving these outcomes. This study highlights the efficacy of small molecule drugs and novel selective interleukin-23s as alternatives to other biologics.
中重度溃疡性结肠炎(UC)的治疗选择正在迅速增加,但缺乏疗效对比试验使得治疗选择成为一项临床挑战。这项网状荟萃分析旨在比较生物制剂和小分子药物在中重度UC患者实现缓解方面的相对疗效。
检索截至2024年5月的文献。纳入3期安慰剂或活性对照随机对照试验。主要结局是诱导并维持内镜改善(梅奥内镜评分[MES]≤1)。次要结局是诱导并维持临床缓解、内镜缓解(MES = 0)和组织学缓解。根据随机对照试验设计和既往生物治疗暴露情况进行亚组分析。
我们确定了36项符合纳入标准的研究,涉及14270例UC患者。乌帕替尼在诱导临床缓解(99.6%)和内镜改善(99.2%)方面排名最高,其次分别是瑞莎珠单抗(91.4%)和(82.3%)。在维持内镜改善方面,乌帕替尼排名第一(98.6%),其次是200mg非戈替尼(79.2%)。瑞莎珠单抗在诱导组织学缓解方面排名第一(89.4%),其次是古塞库单抗(88.3%)。乌帕替尼在维持组织学缓解方面排名第一(93.1%),其次是古塞库单抗(89.5%)。
在实现临床缓解、内镜改善与缓解以及组织学缓解方面,乌帕替尼似乎优于其他疗法。此外,瑞莎珠单抗和古塞库单抗等新型生物制剂在实现这些结局方面排名靠前。本研究突出了小分子药物和新型选择性白细胞介素-23作为其他生物制剂替代品的疗效。