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网络荟萃分析:溃疡性结肠炎中高级治疗的组织学和组织内镜改善及缓解情况。

Network Meta-Analysis: Histologic and Histo-Endoscopic Improvement and Remission With Advanced Therapy in Ulcerative Colitis.

机构信息

Department of Gastroenterology, Unidade Local de Saúde Gaia Espinho, Vila Nova de Gaia, Portugal.

Department of Biomedicine, Unit of Pharmacology and Therapeutics, Faculty of Medicine, University of Porto, Porto, Portugal.

出版信息

Aliment Pharmacol Ther. 2024 Nov;60(10):1276-1292. doi: 10.1111/apt.18315. Epub 2024 Oct 5.

Abstract

BACKGROUND

Histology has prognostic value in ulcerative colitis (UC). However, direct comparisons of histological endpoints are lacking.

AIM

To perform a network meta-analysis (NMA) to compare histological endpoints with biologics and small molecules.

METHODS

We searched four databases up until July 2024 for randomised controlled trials (RCTs) on advanced therapies for moderate-to-severe UC reporting histological endpoints. Outcomes included histological improvement or remission, and histo-endoscopic improvement after induction or during maintenance. We used a random-effects frequentist model and have reported outcomes as relative risk and 95% confidence interval. We estimated relative drug efficacy with the P-score. We conducted subgroup analysis by trial phase and evaluated risk of bias and evidence certainty.

RESULTS

We included 24 RCTs (15 therapies, 8874 patients). Nineteen provided data on induction and 10 on maintenance; outcome definitions were similar. Etrasimod 2 mg/day ranked highest in achieving histologic improvement (P-score 0.98) and remission (P-score 0.90) following induction. Globally, guselkumab 200-400 mg ranked first for histo-endoscopic improvement, while etrasimod 2 mg/day and upadacitinib 45 mg/day were superior in the subgroup analysis. During maintenance, upadacitinib 30 mg/day was superior in achieving histologic improvement and remission (P-score 0.88 for both) and histo-endoscopic improvement (P-score 0.94). Etrasimod 2 mg/day ranked second for histologic remission (P-score 0.70) and histo-endoscopic improvement (P-score 0.73), while mirikizumab 200 mg/month ranked second for histologic improvement.

CONCLUSION

These results support the ability of small molecules to achieve stringent endpoints in moderate-to-severe UC. Histological outcome data for biologics was sparser, particularly during maintenance. Head-to-head RCTs are imperative to better inform clinical practice.

摘要

背景

组织学在溃疡性结肠炎(UC)中具有预后价值。然而,缺乏对组织学终点的直接比较。

目的

进行网络荟萃分析(NMA)以比较生物制剂和小分子的组织学终点。

方法

我们在截至 2024 年 7 月的时间内,在四个数据库中搜索了关于中重度 UC 的高级治疗的随机对照试验(RCT),报告了组织学终点。结果包括诱导后和维持期的组织学改善或缓解,以及组织内镜改善。我们使用随机效应似然比法和报告了相对风险和 95%置信区间。我们使用 P 评分估计相对药物疗效。我们进行了试验阶段的亚组分析,并评估了偏倚风险和证据确定性。

结果

我们纳入了 24 项 RCT(15 种疗法,8874 名患者)。19 项提供了诱导后的数据,10 项提供了维持期的数据;结果定义相似。依特司单抗 2mg/天在诱导后实现组织学改善(P 评分 0.98)和缓解(P 评分 0.90)方面排名最高。总体而言,古塞库单抗 200-400mg 在组织内镜改善方面排名第一,而依特司单抗 2mg/天和乌帕达昔单抗 45mg/天在亚组分析中更优。在维持期,乌帕达昔单抗 30mg/天在实现组织学改善和缓解(P 评分分别为 0.88 和 0.88)和组织内镜改善(P 评分 0.94)方面更优。依特司单抗 2mg/天在组织学缓解(P 评分 0.70)和组织内镜改善(P 评分 0.73)方面排名第二,而米库木单抗 200mg/月在组织学改善方面排名第二。

结论

这些结果支持小分子在中重度 UC 中达到严格终点的能力。生物制剂的组织学结果数据更为稀少,特别是在维持期。头对头 RCT 对于更好地指导临床实践至关重要。

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