Taxonera Carlos, García-Brenes Miguel A, Machín María, Olivares David, López-García Olga N, Zapater Raúl, Alba Cristina
Inflammatory Bowel Disease Unit, Gastroenterology Department, Hospital Clínico San Carlos, 28040 Madrid, Spain.
Instituto de Investigación del Hospital Clínico San Carlos [IdISSC], 28040 Madrid, Spain.
J Clin Med. 2025 Mar 25;14(7):2232. doi: 10.3390/jcm14072232.
: Evidence is needed on the real-world outcomes of upadacitinib in patients with ulcerative colitis. This systematic review and meta-analysis evaluated the real-world effectiveness of upadacitinib for active UC. : The primary outcome was clinical remission evaluated at week 8. Secondary outcomes included response, steroid-free remission, biochemical remission, colectomy, and safety. A random-effects meta-analysis model was used to calculate the pooled effect sizes (percentages or incidence rates) of effectiveness and safety outcomes. : Twenty-four studies with 1388 patients were included. Ninety-four percent of patients had previously failed biologics or Janus kinase inhibitors (JAKi), including 53.2% with tofacitinib. Clinical remission at week 8 was achieved in 68.4% of patients (95% confidence interval 55.5-80.2). Clinical remission was achieved in 48.3%, 71.1%, and 64.6% of patients at weeks 2 to 6, 12 to 16, and 24 to 36, respectively. Response was achieved in 72.6%, 82.1%, and 78.7% of patients at weeks 2 to 6, week 8, and weeks 12 to 16, respectively. Steroid-free remission was achieved in 39% of patients at week 8. Upadacitinib results were unaffected by prior biologic or JAKi failure. Mean fecal calprotectin level decreased from 1485.0 µ/g at baseline to 454.8 µ/g post-treatment ( < 0.01). The mean CRP level decreased from 12.3 mg/L at baseline to 4.4 mg/L post-treatment ( = 0.02). The incidence rates of colectomy, serious adverse events, and herpes zoster were 13.3, 2.3, and 1.7 per 100 patient-years, respectively. : This meta-analysis confirms the effectiveness and safety of upadacitinib in a highly treatment-refractory population of UC patients.
需要有关乌帕替尼治疗溃疡性结肠炎患者的真实世界结局的证据。本系统评价和荟萃分析评估了乌帕替尼治疗活动性溃疡性结肠炎的真实世界有效性。主要结局是在第8周评估的临床缓解。次要结局包括缓解、无类固醇缓解、生化缓解、结肠切除术和安全性。采用随机效应荟萃分析模型计算有效性和安全性结局的合并效应量(百分比或发生率)。纳入了24项研究,共1388例患者。94%的患者既往使用生物制剂或 Janus 激酶抑制剂(JAKi)治疗失败,其中53.2%的患者使用托法替布治疗失败。68.4%的患者在第8周实现临床缓解(95%置信区间55.5 - 80.2)。在第2至6周、第12至16周和第24至36周,分别有48.3%、71.1%和64.6%的患者实现临床缓解。在第2至6周、第8周和第12至16周,分别有72.6%、82.1%和78.7%的患者实现缓解。39%的患者在第8周实现无类固醇缓解。乌帕替尼的疗效不受既往生物制剂或JAKi治疗失败的影响。粪便钙卫蛋白平均水平从基线时的1485.0µ/g降至治疗后的454.8µ/g(P < 0.01)。C反应蛋白平均水平从基线时的12.3mg/L降至治疗后的4.4mg/L(P = 0.02)。结肠切除术、严重不良事件和带状疱疹的发生率分别为每100患者年13.3、2.3和1.7。这项荟萃分析证实了乌帕替尼在高度难治性溃疡性结肠炎患者群体中的有效性和安全性。