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比较 risankizumab 和 ustekinumab 诱导和维持治疗中重度活动期克罗恩病的匹配调整间接比较。

Matching-Adjusted Indirect Comparison Between Risankizumab and Ustekinumab for Induction and Maintenance Treatment of Moderately to Severely Active Crohn's Disease.

机构信息

Department of Pediatrics, Susan and Leonard Feinstein IBD Center, Icahn School of Medicine, Mount Sinai, New York, NY, USA.

Division of Gastroenterology & Hepatology, Departments of Medicine & Community Health Sciences, University of Calgary, Calgary, AB, Canada.

出版信息

Adv Ther. 2023 Sep;40(9):3896-3911. doi: 10.1007/s12325-023-02546-6. Epub 2023 Jun 27.

Abstract

INTRODUCTION

Risankizumab (RZB) and ustekinumab (UST), interleukin (IL)-23 and IL-12/23 inhibitors, respectively, are approved treatments for moderately to severely active Crohn's disease (CD); direct comparison between the two is ongoing. We indirectly compared efficacy of RZB versus UST using data from phase 3 trials (RZB: NCT03104413; NCT03105128; NCT03105102; UST: NCT01369329; NCT01369342; NCT01369355).

METHODS

Matching-adjusted indirect comparison was conducted using individual patient-level data from RZB trials and published aggregated data from UST trials. During induction, patients received RZB 600 mg intravenous (IV) at weeks 0, 4, and 8 or a single dose of UST 6 mg/kg IV at week 0. During maintenance, patients received RZB 180 or 360 mg subcutaneous (SC) or UST 90 mg SC every 8 or 12 weeks to 52 weeks. Outcomes included proportion of patients achieving Crohn's Disease Activity Index (CDAI) response (decrease of ≥ 100 points or total score < 150) or remission (CDAI ≤ 150) and endoscopic improvement (measured by the Simple Endoscopic Score in CD [SES-CD]; response, ≥ 50% reduction from baseline; remission, SES-CD ≤ 2) following induction/baseline.

RESULTS

Higher proportions of patients achieved clinical and endoscopic outcomes with RZB vs. UST induction treatment, resulting in significantly (p ≤ 0.05) greater percent differences (95% confidence intervals) between groups for CDAI remission (15% [5%, 25%]) and endoscopic response (26% [13%, 40%]) and remission (9% [0%, 19%]). Following maintenance, rates of CDAI remission were similar (range - 0.3% to - 5.0%) for RZB vs. UST. Differences for endoscopic response and remission ranged from 9.3% to 27.7% and 11.6% to 12.5%, respectively; differences were significant (p < 0.05) for endoscopic response for both doses of RZB compared to UST 12-week dosing.

CONCLUSIONS

This indirect comparison demonstrated higher rates of clinical and endoscopic outcomes during induction for RZB compared to UST; CDAI remission following maintenance was comparable. Direct comparisons of RZB and UST are warranted to validate these findings.

摘要

简介

利纳西普(RZB)和乌司奴单抗(UST)分别是白细胞介素(IL)-23 和 IL-12/23 抑制剂,适用于中重度活动期克罗恩病(CD)的治疗;目前正在对两者进行直接比较。我们使用来自 3 期试验的个体患者水平数据(RZB:NCT03104413;NCT03105128;NCT03105102;UST:NCT01369329;NCT01369342;NCT01369355),对 RZB 与 UST 的疗效进行了间接比较。

方法

使用 RZB 试验的个体患者水平数据和 UST 试验的已发表汇总数据进行匹配调整间接比较。诱导期时,患者接受 RZB 600mg 静脉注射(IV),分别在第 0、4 和 8 周,或单次给予 UST 6mg/kg IV,在第 0 周。维持期时,患者接受 RZB 180 或 360mg 皮下(SC)或 UST 90mg SC,每 8 或 12 周给药一次,共 52 周。结局包括达到克罗恩病活动指数(CDAI)缓解(下降≥100 分或总分<150)或缓解(CDAI≤150)和内镜改善(采用 CD 简单内镜评分[SES-CD]衡量;缓解,基线降低≥50%;缓解,SES-CD≤2)的患者比例。

结果

与 UST 诱导治疗相比,RZB 诱导治疗有更高比例的患者达到临床和内镜结局,导致 CDAI 缓解(15%[5%,25%])和内镜缓解(26%[13%,40%])和缓解(9%[0%,19%])的组间差异有统计学意义(p≤0.05)。维持治疗后,RZB 与 UST 的 CDAI 缓解率相似(范围-0.3%至-5.0%)。内镜缓解和缓解率的差异范围为 9.3%至 27.7%和 11.6%至 12.5%;与 UST 12 周剂量相比,RZB 两种剂量的内镜缓解差异均有统计学意义(p<0.05)。

结论

这项间接比较表明,与 UST 相比,RZB 在诱导期有更高的临床和内镜结局;维持治疗后的 CDAI 缓解率相当。需要对 RZB 和 UST 进行直接比较,以验证这些发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1f27/10427520/1b02a78b6e95/12325_2023_2546_Fig1_HTML.jpg

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