Feng Haihuan, Zhao Ying, Kuang Weihong, Dai Yanping, Cen Xiaobo, Qin Feng
State Key Laboratory of Biotherapy, Collaborative Innovation Center for Biotherapy, National Chengdu Center for Safety Evaluation of Drugs, West China Hospital, Sichuan University, Chengdu, China.
Medical Insurance Office, West China Hospital, Sichuan University, Chengdu, China.
Front Pharmacol. 2023 Feb 13;14:1084614. doi: 10.3389/fphar.2023.1084614. eCollection 2023.
Tumor necrosis factor alpha inhibitors (TNFi) have shown substantial efficacy in alleviating and treating ankylosing spondylitis (AS). However, the heightened interest is accompanied by concerns over adverse events. In this meta-analysis, we analyzed both serious and common adverse events in patients treated with tumor necrosis factor alpha inhibitors compared with those in the placebo group. We searched for clinical trials in PubMed, Embase, Cochrane Library, China National Knowledge Infrastructure, Wanfang Data, and VIP Data. Studies were selected based on strict inclusion and exclusion criteria. Only randomized, placebo-controlled trials were included in the final analysis. RevMan 5.4 software was used for performing meta-analyses. A total of 18 randomized controlled trials recruiting 3,564 patients with ankylosing spondylitis were included, with overall moderate to high methodological quality. Compared with the placebo group, the incidences showed no difference and were only slightly increased numerically for serious adverse events, serious infections, upper respiratory tract infection, and malignancies in patients treated with tumor necrosis factor alpha inhibitors. However, tumor necrosis factor alpha inhibitor treatment significantly increased the incidence of overall adverse events, nasopharyngitis, headache, and injection-site reactions in ankylosing spondylitis patients when compared with placebo. The available data indicated that ankylosing spondylitis patients who received tumor necrosis factor alpha inhibitors had no significantly increased risks of serious adverse events when compared with the placebo group. However, tumor necrosis factor alpha inhibitors significantly increased the incidence rate of common adverse events, including nasopharyngitis, headache, and injection-site reactions. Large-scale and long-term follow-up clinical trials are still necessary to further investigate the safety of tumor necrosis factor alpha inhibitors in ankylosing spondylitis treatment.
肿瘤坏死因子α抑制剂(TNFi)在缓解和治疗强直性脊柱炎(AS)方面已显示出显著疗效。然而,人们在对此兴趣大增的同时,也对不良事件有所担忧。在这项荟萃分析中,我们分析了接受肿瘤坏死因子α抑制剂治疗的患者与安慰剂组患者的严重不良事件和常见不良事件。我们在PubMed、Embase、Cochrane图书馆、中国知网、万方数据和维普数据中检索临床试验。研究根据严格的纳入和排除标准进行筛选。最终分析仅纳入随机、安慰剂对照试验。使用RevMan 5.4软件进行荟萃分析。共纳入18项招募了3564例强直性脊柱炎患者的随机对照试验,总体方法学质量为中度至高。与安慰剂组相比,接受肿瘤坏死因子α抑制剂治疗的患者在严重不良事件、严重感染、上呼吸道感染和恶性肿瘤方面的发生率无差异,仅在数值上略有增加。然而,与安慰剂相比,肿瘤坏死因子α抑制剂治疗显著增加了强直性脊柱炎患者总体不良事件、鼻咽炎、头痛和注射部位反应的发生率。现有数据表明,与安慰剂组相比,接受肿瘤坏死因子α抑制剂治疗的强直性脊柱炎患者发生严重不良事件的风险没有显著增加。然而,肿瘤坏死因子α抑制剂显著增加了包括鼻咽炎、头痛和注射部位反应在内的常见不良事件的发生率。仍有必要进行大规模、长期随访的临床试验,以进一步研究肿瘤坏死因子α抑制剂在强直性脊柱炎治疗中的安全性。