Corticosteroid-sparing effects of risankizumab efficacy and safety in patients with moderately to severely active ulcerative colitis.

Walter Reinisch, Edward V Loftus, Stefan Schreiber, David T Rubin, Edouard Louis, Patrick M Hecht, Elena Marced Barrachina, Jasmina Kalabic, Ramona Vladea, Dolly Sharma, Weijiang Rachel Duan, Yafei Zhang, Remo Panaccione
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Abstract

Background and aims: This post hoc analysis evaluated the corticosteroid-sparing effects of risankizumab (RZB) therapy in patients with moderate-to-severe ulcerative colitis in the phase 3 induction and maintenance studies, INSPIRE and COMMAND.

Methods: Patients were randomized (2:1) to 12 weeks of intravenous RZB or placebo (PBO) induction therapy; responders to intravenous RZB were randomized (1:1:1) to receive subcutaneous RZB 180 mg, 360 mg, or PBO (RZB withdrawal) maintenance therapy. Baseline corticosteroid doses were maintained during induction, with a mandatory taper beginning at maintenance week 0. Efficacy outcomes were evaluated by baseline corticosteroid use at induction week 12, while corticosteroid-free clinical and endoscopic outcomes were assessed at maintenance week 52 among the overall population and among patients on corticosteroids at baseline. Safety was also assessed.

Results: At baseline, 35.7% (348/975) of patients were taking corticosteroids. At induction week 12, greater rates were observed for clinical, endoscopic, and patient-reported outcomes in RZB 1200 mg-treated patients compared with PBO, regardless of baseline corticosteroid use. RZB 180 mg and 360 mg treatment resulted in higher corticosteroid discontinuation rates (RZB 180 mg 64.9% [48/74]; RZB 360 mg 54.2% [32/59]; PBO [withdrawal] 36.8% [25/68], P ≤ .01) and corticosteroid-free clinical, endoscopic, and patient-reported outcomes at week 52, compared with PBO (withdrawal). The rates of treatment-emergent adverse events were similar regardless of baseline corticosteroid use during induction and maintenance.

Conclusions: The efficacy of RZB induction therapy was independent of corticosteroid use, with high rates of corticosteroid-free outcomes observed in the overall population and among patients with baseline corticosteroid use, reaffirming the potential of RZB to serve as a corticosteroid-sparing therapy for patients with ulcerative colitis.

Clinicaltrial.gov numbers: NCT03398148 and NCT03398135.

中度至重度活动性溃疡性结肠炎患者的利桑单抗疗效和安全性对皮质类固醇的影响。
背景和目的:在INSPIRE和COMMAND的3期诱导和维持研究中,本事后分析评估了risankizumab (RZB)治疗中重度溃疡性结肠炎患者的皮质激素节约效果。方法:患者随机(2:1)至12周静脉注射RZB或安慰剂(PBO)诱导治疗;静脉注射RZB应答者随机(1:1:1)接受皮下RZB 180 mg、360 mg或PBO (RZB戒断)维持治疗。诱导期间维持基线皮质类固醇剂量,从维持第0周开始强制逐渐减少。在诱导治疗第12周时,通过基线皮质类固醇使用来评估疗效结果,而在维持治疗第52周时,对总体人群和基线使用皮质类固醇的患者进行无皮质类固醇临床和内窥镜结果评估。安全性也进行了评估。结果:基线时,35.7%(348/975)的患者服用皮质类固醇。在诱导第12周,与PBO相比,rzb1200mg治疗的患者在临床、内窥镜和患者报告的结果中观察到更高的发生率,无论基线皮质类固醇使用情况如何。RZB 180 mg和360 mg治疗导致更高的皮质类固醇停药率(RZB 180 mg 64.9% [48/74];RZB 360 mg 54.2% [32/59];与PBO(停药)相比,PBO[停药]36.8% [25/68],P≤0.01)和52周无皮质类固醇的临床、内镜和患者报告结果。无论诱导和维持期间基线皮质类固醇使用情况如何,治疗后出现的不良事件发生率相似。结论:RZB诱导治疗的疗效与皮质类固醇的使用无关,在总体人群和基线使用皮质类固醇的患者中观察到高比例的无皮质类固醇结果,重申了RZB作为溃疡性结肠炎患者保留皮质类固醇治疗的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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