Department of Ophthalmology, Ankang Hospital of Traditional Chinese Medicine, No. 47 Bashan East Rd., Hanbin Dist, Ankang City, 725000, China.
Wenzhou Medical University, Wenzhou, China.
BMC Ophthalmol. 2023 May 29;23(1):240. doi: 10.1186/s12886-023-02987-1.
To compare the efficacy and safety of infliximab with that of adalimumab in the treatment of non-infectious uveitis (NIU).
We searched for relevant studies in the PubMed, Embase, ClinicalTrials.gov, Cochrane Library databases, Grey Matters, Grey Literature Report, OpenGrey, China National Knowledge Infrastructure (CNKI), and Wan Fang databases up to September 2022. The incidences of complete remission of inflammation, response to therapy, adverse events and corticosteroid-sparing effect were evaluated.
Eleven clinical trials covering 1459 NIU patients were included. Complete remission of inflammation after therapy was achieved in 161 (37.5%) patients in the infliximab group and 151 (39.6%) patients in the adalimumab group. These two groups were not significantly different (P = 0.37). Four studies reported response to anti-TNF therapy involving 449 patients, of whom 241/272 (88.6%) treated with infliximab and 153/177 (86.4%) treated with adalimumab achieved partial or complete remission of inflammation. No significant difference was observed between the two cohorts in terms of response to therapy (P = 0.86). There was no significant difference between infliximab and adalimumab with regard to corticosteroid-sparing effect (P = 0.58). The pooled effect size (P = 0.001) showed a statistically significant difference, with the incidence of adverse events being 17.91% for infliximab and 12.12% for adalimumab.
Our systematic review and meta-analysis of 11 studies suggests that infliximab and adalimumab have similar therapeutic efficacy and corticosteroid-sparing effect in patients with NIU. However, adalimumab has a marginal advantage over infliximab in terms of adverse events. Large-scale RCTs with a longer follow-up are required to further evaluate these two anti-TNF-α agents in patients with NIU.
比较英夫利昔单抗与阿达木单抗治疗非感染性葡萄膜炎(NIU)的疗效和安全性。
我们检索了 PubMed、Embase、ClinicalTrials.gov、Cochrane 图书馆、Grey Matters、Grey Literature Report、OpenGrey、中国知网(CNKI)和万方数据库,检索时间截至 2022 年 9 月。评估炎症完全缓解率、治疗反应、不良反应和皮质类固醇节省效应。
纳入了 11 项临床试验,共纳入 1459 例 NIU 患者。英夫利昔单抗组 161 例(37.5%)和阿达木单抗组 151 例(39.6%)患者治疗后炎症完全缓解,两组差异无统计学意义(P=0.37)。4 项研究报告了抗 TNF 治疗反应,涉及 449 例患者,其中英夫利昔单抗治疗组 241/272(88.6%)和阿达木单抗治疗组 153/177(86.4%)患者炎症部分或完全缓解,两组治疗反应差异无统计学意义(P=0.86)。英夫利昔单抗和阿达木单抗在皮质类固醇节省效应方面无差异(P=0.58)。汇总效应量(P=0.001)显示有统计学意义的差异,英夫利昔单抗组不良反应发生率为 17.91%,阿达木单抗组为 12.12%。
本系统评价和荟萃分析纳入 11 项研究,结果表明,英夫利昔单抗和阿达木单抗治疗 NIU 患者的疗效和皮质类固醇节省效应相似,但阿达木单抗在不良反应方面略优于英夫利昔单抗。需要开展更大规模的 RCT 并进行更长时间的随访,以进一步评估这两种抗 TNF-α 药物在 NIU 患者中的应用。