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炎症性肠病的高级治疗中匹配的 2 期和 3 期试验的治疗效果大小比较:系统评价和荟萃分析。

A Comparison of Treatment Effect Sizes in Matched Phase 2 and Phase 3 Trials of Advanced Therapeutics in Inflammatory Bowel Disease: Systematic Review and Meta-Analysis.

机构信息

Department of Gastroenterology and Hepatology, University Medical Center Ljubljana, Ljubljana, Slovenia.

Alimentiv Inc, London, Ontario, Canada.

出版信息

Clin Transl Gastroenterol. 2023 Nov 1;14(11):e00629. doi: 10.14309/ctg.0000000000000629.

Abstract

INTRODUCTION

Phase 2 trials are fundamental to the rational and efficient design of phase 3 trials. We aimed to determine the relationship of treatment effect size estimates from phase 2 and phase 3 clinical trials on advanced therapeutics in inflammatory bowel disease.

METHODS

MEDLINE, EMBASE, CENTRAL, and the Cochrane library were searched from inception to December 19, 2022, to identify paired phase 2 and 3 placebo-controlled induction studies of advanced therapeutics for Crohn's disease (CD) and ulcerative colitis (UC). Treatment effect sizes were expressed as a risk ratio (RR) between the active arm and placebo arm. For the same therapeutics, RRs from phase 2 trials were divided by the RR from phase 3 trial to quantify the relationship of effect sizes between phases.

RESULTS

Twenty-two studies (9 phase 2 trials, 13 phase 3 trials) were included for CD and 30 studies (12 phase 2 trials, 18 phase 3 trials) for UC. In UC (pooled RR 0.72; 95% confidence interval: 0.58-0.86; RR <1 indicates smaller treatment effect sizes in phase 2 trials), but not CD (pooled RR 1.01; 95% confidence interval: 0.84-1.18), phase 2 trials systematically underestimated treatment effect sizes for the primary endpoint compared with phase 3 trials. The underestimation was observed for clinical, but not endoscopic, endpoints in UC.

DISCUSSION

Treatment effect sizes for the primary and clinical endpoints were similar across clinical trial phases in CD, but not UC, where only endoscopic endpoints were comparable. This will help inform clinical development plans and future trial design.

摘要

简介

二期临床试验对于三期临床试验的合理和高效设计至关重要。我们旨在确定炎症性肠病(IBD)中高级治疗药物的二期和三期临床试验的治疗效果估计值之间的关系。

方法

从 1975 年 1 月至 2022 年 12 月 19 日,我们在 MEDLINE、EMBASE、CENTRAL 和 Cochrane 图书馆中搜索了配对的二期和三期安慰剂对照诱导研究,以确定克罗恩病(CD)和溃疡性结肠炎(UC)高级治疗药物的二期和三期临床试验。治疗效果大小表示为活性臂与安慰剂臂之间的风险比(RR)。对于相同的治疗药物,将二期试验的 RR 除以三期试验的 RR,以量化两期之间的效果大小关系。

结果

纳入了 22 项研究(9 项二期试验,13 项三期试验)用于 CD,30 项研究(12 项二期试验,18 项三期试验)用于 UC。在 UC(汇总 RR0.72;95%置信区间:0.58-0.86;RR<1 表示二期试验中治疗效果较小),但不是 CD(汇总 RR1.01;95%置信区间:0.84-1.18)中,二期试验系统地低估了主要终点的治疗效果与三期试验相比。在 UC 中观察到临床终点,而不是内镜终点的低估。

讨论

在 CD 中,主要和临床终点的治疗效果在临床试验阶段相似,但在 UC 中并非如此,只有内镜终点可以比较。这将有助于为临床开发计划和未来的试验设计提供信息。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1ae8/10684248/618c4db1eb84/ct9-14-e00629-g001.jpg

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