优思明单抗治疗炎症性肠病的安全性:对克罗恩病治疗 5 年和溃疡性结肠炎治疗 4 年的汇总安全性分析。

Subrata Ghosh, Brian G Feagan, Elyssa Ott, Christopher Gasink, Bridget Godwin, Colleen Marano, Ye Miao, Tony Ma, Edward V Loftus, William J Sandborn, Silvio Danese, Maria T Abreu, Bruce E Sands
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引用次数: 0

摘要

背景和目的:此前公布的长期安全性数据显示,乌司替尼治疗炎症性肠病(IBD)具有良好的安全性。我们将汇总乌斯特库单抗治疗克罗恩病(CD)5年和治疗溃疡性结肠炎(UC)4年的IBD 2/3期临床研究的最终累积安全性数据:在3期研究中,患者接受单次静脉注射安慰剂或乌斯特库单抗(130 毫克或约 6 毫克/千克)诱导剂量,然后皮下注射安慰剂或乌斯特库单抗维持剂量(90 毫克 q8w 或 q12w)。分析包括所有接受过一剂研究治疗的患者,也包括生物制剂无效的患者和有生物制剂失败史的患者。安全性结果以每100例患者随访年发生的事件数和相应的95%置信区间进行总结和展示:在这项最终的汇总安全性分析中,2575名患者接受了乌司替尼治疗,随访时间为4826年。包括MACE和恶性肿瘤在内的主要安全事件发生率与安慰剂和乌司替库单抗相似,乌司替库单抗的发生率并不高。在IBD组的关键安全事件发生率方面,无论是生物制剂新药患者还是之前使用生物制剂失败的患者,乌司替库单抗组均不高于安慰剂组。没有淋巴瘤或后遗可逆性脑病综合征(PRES,以前称为可逆性后遗白质脑病综合征[RPLS])病例的报道:与安慰剂相比,乌斯特库单抗在 CD 中 5 年的最终累积安全性数据和在 UC 中 4 年的最终累积安全性数据均显示出良好的安全性,并继续支持其在所有已批准适应症中行之有效的安全性特征。
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Safety of Ustekinumab in Inflammatory Bowel Disease: Pooled Safety Analysis Through 5 Years in Crohn's Disease and 4 Years in Ulcerative Colitis.

Background and aims: Previously published long-term safety data reported a favourable ustekinumab safety profile for the treatment of inflammatory bowel disease [IBD]. We present the final cumulative safety data from pooled ustekinumab IBD phase 2/3 clinical studies through 5 years in Crohn's disease [CD] and 4 years in ulcerative colitis [UC].

Methods: In phase 3 studies, patients received a single intravenous placebo or ustekinumab [130 mg or ~6 mg/kg] induction dose followed by subcutaneous maintenance doses of placebo or ustekinumab [90 mg q8w or q12w]. Analyses included all patients who received one dose of study treatment and included patients who were biologic-naïve and patients with a history of biologic failure. Safety outcomes are summarized and presented using number of events per 100 patient-years of follow-up and corresponding 95% confidence intervals.

Results: In this final pooled safety analysis, 2575 patients were treated with ustekinumab with 4826 patient-years of follow-up. Rates of key safety events, including major adverse cardiac events and malignancies, were similar between placebo and ustekinumab or not higher for ustekinumab. Opportunistic infections, including tuberculosis, and malignancies were reported infrequently. Rates of key safety events in the IBD group were no higher in the ustekinumab group than in the placebo group for both patients who were biologic-naïve or who had a history of biologic failure. No lymphomas or cases of posterior reversible encephalopathy syndrome [formerly known as reversible posterior leukoencephalopathy syndrome] were reported.

Conclusion: The final cumulative ustekinumab safety data through 5 years in CD and 4 years in UC demonstrated favourable safety compared to placebo and continue to support the well-established safety profile across all approved indications.

Clinical trials.gov numbers: NCT00265122, NCT00771667, NCT01369329, NCT01369342, NCT01369355, NCT02407236.

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