Etrolizumab as an induction and maintenance therapy for ulcerative colitis: A systematic review and meta-analysis of randomized controlled trials

IF 1.7 Q3 GASTROENTEROLOGY & HEPATOLOGY
JGH Open Pub Date : 2024-04-02 DOI:10.1002/jgh3.13056
Othman Saleh, Mohamed T. Abuelazm, Islam Mohamed, Alaa Ramadan, Mohammad Assaf, Ahmad Alzoubi, Majd M. AlBarakat, Basel Abdelazeem
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引用次数: 0

Abstract

Background and Aim

Etrolizumab is a gut-targeted anti-β7 integrin monoclonal antibody. However, the evidence of etrolizumab efficacy and safety in ulcerative colitis remains inconclusive. Therefore, we aim to evaluate the safety and efficacy of etrolizumab as an induction and maintenance therapy for active moderate to severe ulcerative colitis.

Methods

We synthesized randomized controlled studies (RCTs) from MEDLINE, Scopus, EMBASE, PubMed, Web of Science, and Cochrane Library until April 2023. The risk ratio (RR) for dichotomous outcomes with the corresponding 95% confidence interval (CI) was used. The study protocol was registered in PROSPERO with ID: CRD42023437040.

Results

Five RCTs with 1849 participants were included. The etrolizumab group had a significant clinical response (RR: 1.28 with 95% CI [1.08, 1.51], P = 0.005), clinical remission rates during the induction phase (RR: 2.47 with 95% CI [1.48, 4.11], P = 0.0005), compared with the placebo group in ulcerative colitis; however, there was no statistically significant difference between the two groups, regarding the corticosteroids-free remission rate (RR: 1.92 with 95% CI [0.94, 3.92], P = 0.07). Moreover, endoscopic improvement, endoscopic remission, and histologic remission rates were observed more in the etrolizumab group during both the induction and maintenance phases. For safety outcomes, etrolizumab was significantly safer, but any adverse event was higher in the etrolizumab group than in the placebo.

Conclusion

Etrolizumab shows its effectiveness as both an induction and maintenance therapy for moderate or severe UC. The findings demonstrate its positive impact on clinical, endoscopic, and histologic remission rates. Regarding safety, other than any side effects, etrolizumab showed a good safety than a placebo.

Abstract Image

依托利珠单抗作为溃疡性结肠炎的诱导和维持疗法:随机对照试验的系统回顾和荟萃分析
背景和目的 依托珠单抗是一种肠道靶向抗β7整合素单克隆抗体。然而,etrolizumab 对溃疡性结肠炎的疗效和安全性仍无定论。因此,我们旨在评估依托利珠单抗作为活动性中重度溃疡性结肠炎诱导和维持疗法的安全性和有效性。 方法 我们综合了截至 2023 年 4 月来自 MEDLINE、Scopus、EMBASE、PubMed、Web of Science 和 Cochrane Library 的随机对照研究(RCT)。采用二分法结果的风险比 (RR) 及相应的 95% 置信区间 (CI)。研究方案已在 PROSPERO 注册,ID:CRD42023437040。 结果 共纳入了 5 项 RCT,1849 名参与者。与安慰剂组相比,依托利珠单抗组有显著的临床应答(RR:1.28,95% CI [1.08,1.51],P = 0.005),诱导期临床缓解率(RR:2.47,95% CI [1.48,4.11],P = 0.然而,与安慰剂组相比,两组在无皮质类固醇缓解率(RR:1.92,95% CI [0.94,3.92],P = 0.07)方面没有显著统计学差异。)此外,在诱导和维持阶段,依托利珠单抗组的内镜改善率、内镜缓解率和组织学缓解率都更高。在安全性方面,依托利珠单抗明显更安全,但依托利珠单抗组的任何不良事件均高于安慰剂组。 结论 依托珠单抗在中度或重度 UC 的诱导和维持治疗中均显示出其有效性。研究结果表明,依托珠单抗对临床、内镜和组织学缓解率均有积极影响。在安全性方面,除副作用外,依托珠单抗比安慰剂更安全。
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来源期刊
JGH Open
JGH Open GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
3.40
自引率
0.00%
发文量
143
审稿时长
7 weeks
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