Comparative efficacy and safety of vedolizumab and antitumor necrosis factor alfa in patients with inflammatory bowel diseases: A meta‑analysis.

IF 1.4 4区 医学 Q3 PHARMACOLOGY & PHARMACY Acta Pharmaceutica Pub Date : 2025-04-10 Print Date: 2025-03-01 DOI:10.2478/acph-2025-0004
Yafang Li, Jin Ding, Chong Lu, Yiping Hong, Qunying Wang
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Abstract

This meta-analysis directly compares the efficacy and safety of vedolizumab and tumor necrosis factor-α (TNF-α) inhibitors for patients with inflammatory bowel disease (IBD), contrary to the previous one which provided an indirect comparison. In this meta-analysis, only the studies that directly compared two treatments (vedolizumab and TNF-α inhibitors) to each other (head-to-head approach) were considered. A comprehensive literature search was conducted using the following databases: PubMed, Embase, the Cochrane Library, and Web of Science. The pooled estimates of efficacies and safety were calculated as relative risk (RR) and 95 % confidence interval (CI). The presence of bias in the published material was evaluated using Begg's test. Sensitivity analysis was used to evaluate the pooled results' robustness. In total, 32 eligible studies were finally included. Results showed that the efficacy of vedolizumab was superior to TNF-α inhibitors in clinical remission [1.26, 95 % CI: 1.15-1.39]. Moreover, the vedolizumab group showed a reduced incidence of severe adverse events (RR = 0.63, 95 % CI: 0.42-0.94) compared to TNF-α inhibitors. Our results revealed superior efficacy and safety of vedolizumab compared to TNF-α inhibitors, which provided direct evidence for the use of vedolizumab in IBD treatment. Future studies are needed to confirm our findings.

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vedolizumab和抗肿瘤坏死因子在炎症性肠病患者中的比较疗效和安全性:一项荟萃分析
这项荟萃分析直接比较了vedolizumab和肿瘤坏死因子-α (TNF-α)抑制剂治疗炎症性肠病(IBD)患者的疗效和安全性,而不是之前提供的间接比较。在本荟萃分析中,仅考虑了直接比较两种治疗(vedolizumab和TNF-α抑制剂)的研究(头对头方法)。使用以下数据库进行了全面的文献检索:PubMed、Embase、Cochrane图书馆和Web of Science。用相对危险度(RR)和95%置信区间(CI)计算疗效和安全性的综合估计。使用贝格检验评估已发表材料中存在的偏倚。采用敏感性分析评价合并结果的稳健性。最终共纳入32项符合条件的研究。结果显示,vedolizumab在临床缓解方面的疗效优于TNF-α抑制剂[1.26,95% CI: 1.15-1.39]。此外,与TNF-α抑制剂相比,vedolizumab组显示严重不良事件发生率降低(RR = 0.63, 95% CI: 0.42-0.94)。我们的研究结果显示,与TNF-α抑制剂相比,vedolizumab具有更好的疗效和安全性,这为使用vedolizumab治疗IBD提供了直接证据。需要进一步的研究来证实我们的发现。
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来源期刊
Acta Pharmaceutica
Acta Pharmaceutica PHARMACOLOGY & PHARMACY-
CiteScore
5.20
自引率
3.60%
发文量
20
审稿时长
>12 weeks
期刊介绍: AP is an international, multidisciplinary journal devoted to pharmaceutical and allied sciences and contains articles predominantly on core biomedical and health subjects. The aim of AP is to increase the impact of pharmaceutical research in academia, industry and laboratories. With strong emphasis on quality and originality, AP publishes reports from the discovery of a drug up to clinical practice. Topics covered are: analytics, biochemistry, biopharmaceutics, biotechnology, cell biology, cell cultures, clinical pharmacy, drug design, drug delivery, drug disposition, drug stability, gene technology, medicine (including diagnostics and therapy), medicinal chemistry, metabolism, molecular modeling, pharmacology (clinical and animal), peptide and protein chemistry, pharmacognosy, pharmacoepidemiology, pharmacoeconomics, pharmacodynamics and pharmacokinetics, protein design, radiopharmaceuticals, and toxicology.
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