Gao Boyang, Shentu Haojie, Sha Suyong, Wang Dongying, Chen Xi, Huang Zhenwei, Dong Nan, Lai Haijia, Xu Jianying, Zhou Xiaoshuai
Wenzhou Medical University, Wenzhou, Zhejiang, China.
The Medical Imaging College, Hangzhou Medical College, Hangzhou, Zhejiang, China.
Cent Eur J Immunol. 2023;48(4):301-310. doi: 10.5114/ceji.2023.134257. Epub 2024 Jan 9.
A growing number of randomized controlled trials (RCTs) have demonstrated the effectiveness of interleukin (IL)-23 and IL-12/23 inhibitors in treating Crohn's disease (CD). This study evaluated the efficacy of IL-23 and IL-12/23 inhibitors in the induction phase for the treatment of CD.
We searched the following databases from inception until December, 2022: Medline, Embase, Web of Science and the Cochrane Library. The primary outcome was the proportion of CD patients who achieved clinical remission at the end of the induction therapy period. Secondary outcomes included clinical response, endoscopic remission, endoscopic response and normalized C-reactive protein (CRP).
After screening, 7 RCTs were included in our study. The meta-analysis showed that, in the induction period, more patients treated with IL-23 inhibitors and IL-12/23 inhibitors achieved clinical remission than patients with placebo therapy (RR = 2.11, 95% CI: 1.83-2.44; RR = 1.94, 95% CI: 1.64-2.29; respectively). The IL-23 inhibitor group and the IL-12/23 inhibitor group showed higher clinical response rates than the placebo group (RR = 1.92, 95% CI: 1.74-2,11; RR = 1.83, 95% CI: 1.61-2.09; respectively). In addition, the IL-23 inhibitor group had a higher endoscopic remission rate and endoscopic response rate than the placebo group; the corresponding pooled RRs were 3.40 (95% CI: 2.57-4.50) and 2.65 (95% CI: 2.65-3.12), respectively.
IL-23 and IL-12/23 inhibitors were efficient methods in the induction treatment of CD.
越来越多的随机对照试验(RCT)已证明白细胞介素(IL)-23和IL-12/23抑制剂在治疗克罗恩病(CD)方面的有效性。本研究评估了IL-23和IL-12/23抑制剂在CD诱导期治疗中的疗效。
我们检索了从数据库建立至2022年12月的以下数据库:Medline、Embase、科学网和考克兰图书馆。主要结局是在诱导治疗期结束时实现临床缓解的CD患者比例。次要结局包括临床反应、内镜缓解、内镜反应和C反应蛋白(CRP)正常化。
筛选后,本研究纳入了7项RCT。荟萃分析表明,在诱导期,接受IL-23抑制剂和IL-12/23抑制剂治疗的患者比接受安慰剂治疗的患者实现临床缓解的更多(RR = 2.11,95% CI:1.83 - 2.44;RR = 1.94,95% CI:1.64 - 2.29;分别)。IL-23抑制剂组和IL-12/23抑制剂组的临床反应率高于安慰剂组(RR = 1.92,95% CI:1.74 - 2.11;RR = 1.83,95% CI:1.61 - 2.09;分别)。此外,IL-23抑制剂组的内镜缓解率和内镜反应率高于安慰剂组;相应的合并RR分别为3.40(95% CI:2.57 - 4.50)和2.65(95% CI:2.65 - 3.12)。
IL-23和IL-12/23抑制剂是CD诱导治疗中的有效方法。