Division of Gastroenterology, Department of Medicine, Schulich School of Medicine, Western University, London, Ontario, Canada.
Lawson Health Research Institute, Western University, London, Ontario, Canada.
Clin Gastroenterol Hepatol. 2024 Jun;22(6):1190-1199.e15. doi: 10.1016/j.cgh.2023.12.023. Epub 2024 Jan 6.
BACKGROUND & AIMS: We conducted a network meta-analysis to compare the efficacy of advanced therapies for achieving endoscopic outcomes in patients with moderate-to-severely active Crohn's disease.
MEDLINE, Embase, and Cochrane CENTRAL databases were searched from inception to August 2, 2023 to identify phase II and III randomized controlled trials (RCTs) in adults (≥18 years) with moderate-to-severe Crohn's disease treated with tumor necrosis factor (TNF) antagonists, etrolizumab, vedolizumab, anti-interleukin (IL)12/23p40, anti-IL23p19, or Janus kinase-1 (JAK1) inhibitors, compared with placebo/active comparator, for induction and/or maintenance of remission and reported endoscopic outcomes. Primary outcome was endoscopic response after induction therapy, and endoscopic remission after maintenance therapy. We performed a random-effects network meta-analysis using a frequentist approach, and estimated relative risk (RRs), 95% confidence interval (CI) values, and P score for ranking agents. We used GRADE to ascertain certainty of evidence.
A total of 20 RCTs (19 placebo-controlled and 1 head-to-head trial; 5592 patients) were included out of which 12 RCTs reported endoscopic outcomes for the induction phase, 5 reported for the maintenance phase, and 3 reported for both induction and maintenance phases. JAK1 inhibitors (RR, 3·49 [95% CI, 1·48-8·26]) and anti-IL23p19 (RR, 2·30 [95% CI, 1·02-5·18]) agents were more efficacious than etrolizumab (moderate certainty of evidence), and JAK1 inhibitors (RR, 2·34 [95% CI, 1·14-4·80]) were more efficacious than anti-IL12/23p40 agents for inducing endoscopic response (moderate certainty of evidence). JAK1 inhibitors and anti-IL23p19 ranked highest for induction of endoscopic response. There was paucity of RCTs of TNF antagonists reporting endoscopic outcomes with induction therapy. On network meta-analysis of 6 RCTs, all agents except vedolizumab (RR, 1.89 [95% CI, 0.61-5.92]) were effective in maintaining endoscopic remission compared with placebo. TNF antagonists, IL12/23p40, and JAK1 inhibitors were ranked highest.
On network meta-analysis, JAK1 inhibitors and anti-IL23p19 agents may be the most effective among non-TNF-targeting advanced therapies for inducing endoscopic response. Future head-to-head trials will further inform positioning of different therapies for the management of Crohn's disease.
我们进行了一项网络荟萃分析,以比较中重度克罗恩病患者接受高级治疗后内镜结局的疗效。
从建库至 2023 年 8 月 2 日,我们检索了 MEDLINE、Embase 和 Cochrane CENTRAL 数据库,以确定纳入了中重度克罗恩病成人(≥18 岁)的 II 期和 III 期随机对照试验(RCT),这些患者接受肿瘤坏死因子(TNF)拮抗剂、依特罗珠单抗、维得利珠单抗、抗白细胞介素(IL)12/23p40、抗 IL23p19、或 Janus 激酶-1(JAK1)抑制剂治疗,与安慰剂/活性对照相比,用于诱导和/或维持缓解并报告内镜结局。主要结局是诱导治疗后的内镜反应,维持治疗后的内镜缓解。我们使用贝叶斯方法进行了随机效应网络荟萃分析,并估计了相对风险(RR)、95%置信区间(CI)值和用于排名代理的 P 分数。我们使用 GRADE 来确定证据的确定性。
共纳入 20 项 RCT(19 项安慰剂对照和 1 项头对头试验;5592 例患者),其中 12 项 RCT 报告了诱导期的内镜结局,5 项报告了维持期的内镜结局,3 项报告了诱导和维持期的内镜结局。JAK1 抑制剂(RR,3.49 [95%CI,1.48-8.26])和抗 IL23p19(RR,2.30 [95%CI,1.02-5.18])药物比依特罗珠单抗更有效(证据确定性为中度),JAK1 抑制剂(RR,2.34 [95%CI,1.14-4.80])比抗 IL12/23p40 药物更有效诱导内镜反应(证据确定性为中度)。JAK1 抑制剂和抗 IL23p19 在诱导内镜反应方面排名最高。TNF 拮抗剂报告诱导治疗内镜结局的 RCT 较少。在对 6 项 RCT 的网络荟萃分析中,与安慰剂相比,除维得利珠单抗(RR,1.89 [95%CI,0.61-5.92])外,所有药物均能有效维持内镜缓解。TNF 拮抗剂、IL12/23p40 和 JAK1 抑制剂排名最高。
在网络荟萃分析中,JAK1 抑制剂和抗 IL23p19 药物可能是中重度克罗恩病患者非 TNF 靶向高级治疗中诱导内镜反应最有效的药物。未来的头对头试验将进一步为不同治疗方法在克罗恩病管理中的定位提供信息。