Division of Gastroenterology, Department of Medicine, University of California San Diego, La Jolla, California; Division of Biomedical Informatics, Department of Medicine, University of California San Diego, La Jolla, California.
Robert D. and Patricia E. Kern Center for the Science of Health Care Delivery, Mayo Clinic, Rochester, Minnesota.
Clin Gastroenterol Hepatol. 2022 Feb;20(2):e74-e88. doi: 10.1016/j.cgh.2021.02.032. Epub 2021 Feb 25.
We conducted a retrospective cohort study comparing the risk of serious infections between patients treated with tumor necrosis factor-a (TNFa) antagonists vs. vedolizumab in patients with inflammatory bowel diseases (IBD).
Using an administrative claims database, we identified patients with IBD who were new-users of either TNFa antagonists or vedolizumab between 2014-2018 and had insurance coverage for at least 1y before and after treatment initiation. We compared the risk of serious infections (infections requiring hospitalization) between patients treated with vedolizumab or TNFa antagonists using marginal structural Cox proportional hazard models adjusted for baseline disease characteristics, healthcare utilization, comorbidities, and time-varying use of corticosteroids, immunomodulators and opiates.
We included 4881 patients treated with TNFa antagonists (age, 41 ± 15y, 60% with Crohn's disease [CD]) of whom 434 developed serious infections over 5786 person-year [PY] follow-up, and 1106 patients treated with vedolizumab (age, 44 ± 16y, 39% with CD) of whom 86 developed serious infections over 1040-PY follow-up. Vedolizumab was associated with 46% lower risk of serious infections as compared with TNFa antagonists in patients with ulcerative colitis (HR,0.54 [95% CI,0.35-0.83), but no significant differences were observed in patients with CD (HR,1.30 [0.80-2.11]). Vedolizumab was associated with lower risk of extra-intestinal serious infections in patients with UC, but higher risk of gastrointestinal serious infections in patients with CD.
In an observational study of patients with IBD, vedolizumab was associated with lower risk of serious infections as compared with TNFa antagonists, in patients with UC, but not in patients with CD.
我们进行了一项回顾性队列研究,比较了在炎症性肠病(IBD)患者中,使用肿瘤坏死因子-α(TNFa)拮抗剂与 vedolizumab 治疗的患者发生严重感染的风险。
我们使用行政索赔数据库,确定了在 2014-2018 年间新使用 TNFa 拮抗剂或 vedolizumab 的 IBD 患者,并且在治疗开始前和开始后至少有 1 年的保险覆盖。我们使用边缘结构 Cox 比例风险模型比较了接受 vedolizumab 或 TNFa 拮抗剂治疗的患者发生严重感染(需要住院治疗的感染)的风险,该模型调整了基线疾病特征、医疗保健利用、合并症以及皮质类固醇、免疫调节剂和阿片类药物的时间变化使用情况。
我们纳入了 4881 例接受 TNFa 拮抗剂治疗的患者(年龄 41 ± 15 岁,60%为克罗恩病[CD]),其中 434 例在 5786 人年[PY]随访中发生了严重感染,1106 例接受 vedolizumab 治疗的患者(年龄 44 ± 16 岁,39%为 CD),其中 86 例在 1040-PY 随访中发生了严重感染。与 TNFa 拮抗剂相比,vedolizumab 可使溃疡性结肠炎患者严重感染的风险降低 46%(HR,0.54[95%CI,0.35-0.83),但在 CD 患者中未见显著差异(HR,1.30[0.80-2.11)。vedolizumab 与 UC 患者的非肠道严重感染风险降低相关,但与 CD 患者的胃肠道严重感染风险升高相关。
在一项 IBD 患者的观察性研究中,与 TNFa 拮抗剂相比,vedolizumab 可降低 UC 患者严重感染的风险,但不能降低 CD 患者严重感染的风险。