Wu Hongzhen, Xie Tingting, Yu Qiao, Su Tao, Zhang Min, Wu Luying, Wang Xiaoling, Peng Xiang, Zhi Min, Yao Jiayin
Department of Gastroenterology, The Sixth Affiliated Hospital, Sun Yat-Sen University, Guangzhou 515000, China.
Guangdong Provincial Key Laboratory of Colorectal and Pelvic Floor Disease, The Sixth Affiliated Hospital, Sun Yat-Sen University, Guangzhou 515000, China.
Biomedicines. 2025 Jan 14;13(1):190. doi: 10.3390/biomedicines13010190.
Inflammatory bowel disease (IBD) requires effective treatment options. Upadacitinib, a Janus kinase 1 (JAK1) inhibitor, has shown effectiveness in trials for Crohn's disease (CD) and ulcerative colitis (UC). This study evaluates its real-world effectiveness and safety. We conducted a multicenter retrospective cohort study in tertiary care centers, involving patients treated with upadacitinib from January 2023 to September 2024. The study included adult patients aged 18 years or older, diagnosed with UC or CD, who received at least 8 weeks of upadacitinib therapy. Treatment outcomes were evaluated using established clinical, endoscopic, imaging, histological, and laboratory parameters. A total of 236 IBD patients received upadacitinib treatment. In 80 UC patients at 8 weeks, 64.0% achieved steroid-free remission, 57.6% clinical remission, and 81.8% response. Endoscopic remission was 35.8% ( = 0.039), with 63.3% response and 35.8% mucosal healing. Histological remission reached 29.2% ( = 0.009). For 156 CD patients at 12 weeks, 76.8% achieved steroid-free remission ( < 0.001), 77.8% clinical remission ( 0.001), and 81.0% response. Mean CDAI decreased from 214.9 to 117.5 ( < 0.001). Endoscopic remission was 19.4%, with 48.9% response and 4.9% mucosal healing. Radiological remission was 9.1% with 85.7% response. Intestinal ultrasound showed 5.7% remission and 56.7% response. Upadacitinib demonstrates significant real-world effectiveness and safety in IBD, particularly in biologic-resistant cases, as evidenced by high rates of steroid-free remission and clinical response. These outcomes are likely due to its targeted JAK1 inhibition, which effectively reduces inflammation and promotes mucosal healing. Future research should focus on long-term safety, comparative effectiveness with other biologics, and its application in diverse patient populations. These findings support the integration of upadacitinib into IBD management strategies.
炎症性肠病(IBD)需要有效的治疗方案。乌帕替尼是一种 Janus 激酶 1(JAK1)抑制剂,已在克罗恩病(CD)和溃疡性结肠炎(UC)的试验中显示出有效性。本研究评估其在现实世界中的有效性和安全性。我们在三级医疗中心进行了一项多中心回顾性队列研究,纳入了 2023 年 1 月至 2024 年 9 月接受乌帕替尼治疗的患者。该研究包括 18 岁及以上、被诊断为 UC 或 CD 且接受至少 8 周乌帕替尼治疗的成年患者。使用既定的临床、内镜、影像学、组织学和实验室参数评估治疗结果。共有 236 例 IBD 患者接受了乌帕替尼治疗。80 例 UC 患者在 8 周时,64.0%实现了无类固醇缓解,57.6%实现了临床缓解,81.8%有反应。内镜缓解率为 35.8%(P = 0.039),有反应率为 63.3%,黏膜愈合率为 35.8%。组织学缓解率达到 29.2%(P = 0.009)。156 例 CD 患者在 12 周时,76.8%实现了无类固醇缓解(P < 0.001),77.8%实现了临床缓解(P = 0.001),81.0%有反应。平均克罗恩病活动指数(CDAI)从 214.9 降至 117.5(P < 0.001)。内镜缓解率为 19.4%,有反应率为 48.9%,黏膜愈合率为 4.9%。放射学缓解率为 9.1%,有反应率为 85.7%。肠道超声显示缓解率为 5.7%,有反应率为 56.7%。乌帕替尼在 IBD 中显示出显著的现实世界有效性和安全性,尤其是在生物制剂耐药的病例中,无类固醇缓解率和临床反应率高证明了这一点。这些结果可能归因于其对 JAK1 的靶向抑制,有效减轻炎症并促进黏膜愈合。未来的研究应关注长期安全性、与其他生物制剂的比较有效性及其在不同患者群体中的应用。这些发现支持将乌帕替尼纳入 IBD 管理策略。