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