Dalhousie University, Halifax, NS, Canada Probity Medical Research, Waterloo, ON, Canada Tufts Medical Centre, Boston, MA, USA University of Utah Health Sciences Centre, Salt Lake City, UT, USA Northwestern University, Evanston, IL, USA Abbott Laboratories, Abbott Park, IL, USA University of Connecticut School of Medicine, Farmington, CT, USA.
J Eur Acad Dermatol Venereol. 2013 Oct;27(10):1252-61. doi: 10.1111/j.1468-3083.2012.04705.x. Epub 2012 Nov 16.
Anti-interleukin-12/23 treatment (anti-IL-12/23) has recently demonstrated significant efficacy for moderate to severe psoriasis, yet potential safety signals warrant further investigation.
Expand safety findings for the anti-IL-12/23, briakinumab, beyond individual phase II and III clinical trials.
Safety data pooled from five phase II and III clinical trials (parent studies) and an open-label extension study (OLE), through 22 October 2010; patients with ≥ 1 dose of briakinumab in a parent study or the OLE are included. All parent study briakinumab treatment groups were combined with the OLE population, which received 100-mg briakinumab every 4 weeks. Adverse events (AEs) were collected from the first dose of briakinumab, whether in a parent study or the OLE, through 45 days post-last dose.
Two thousand five hundred and twenty patients (4704 patient-years drug exposure) received ≥ 1 dose of briakinumab during the interim period: 5.6% withdrew due to AEs. Serious infections occurred in 1.3% and malignancies in 2.6% (including 1.0% basal cell carcinoma, 0.8% squamous cell carcinoma). Twenty-seven major adverse cardiovascular events (MACE) occurred, seven in one parent study and 20 in the OLE (incidence = 0.57 events/100 PY). Four cardiovascular risk factors were retrospectively found to be significant predictors for MACE during briakinumab exposure: history of cardiovascular disease, diabetes, body mass index (≥ 30) and baseline blood pressure (systolic ≥ 140 or diastolic ≥ 90).
Pooled briakinumab safety results from five parent studies and an OLE suggest increased rates of infections, malignancies and MACE, and that patients receiving anti-IL-12/23 treatment for moderate to severe psoriasis should be monitored for these potential safety signals.
抗白细胞介素-12/23 治疗(抗 IL-12/23)最近对中重度银屑病显示出显著疗效,但潜在的安全信号需要进一步研究。
扩大抗白细胞介素-12/23、布利akinumab 的安全性发现,超出个别二期和三期临床试验。
通过 2010 年 10 月 22 日,对五项二期和三期临床试验(母研究)和一项开放标签扩展研究(OLE)的安全性数据进行了汇总;包括在母研究或 OLE 中接受过≥1 剂布利akinumab 的患者。所有母研究布利akinumab 治疗组均与接受每 4 周 100mg 布利akinumab 的 OLE 人群相结合。从布利akinumab 的首剂开始收集不良事件(AE),无论在母研究还是 OLE 中,直至末次剂量后 45 天。
2520 名患者(4704 患者年药物暴露)在中间期间接受了≥1 剂布利akinumab:5.6%因 AE 而停药。发生严重感染 1.3%,发生恶性肿瘤 2.6%(包括 1.0%基底细胞癌,0.8%鳞状细胞癌)。发生 27 例重大不良心血管事件(MACE),7 例发生在一个母研究中,20 例发生在 OLE 中(发生率=0.57/100PY)。在布利akinumab 暴露期间,回顾性发现四项心血管危险因素是 MACE 的显著预测因素:心血管疾病史、糖尿病、体重指数(≥30)和基线血压(收缩压≥140 或舒张压≥90)。
五项母研究和一项 OLE 的布利akinumab 安全性汇总结果表明,感染、恶性肿瘤和 MACE 的发生率增加,接受中重度银屑病抗白细胞介素-12/23 治疗的患者应监测这些潜在的安全信号。