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评估依曲珠单抗在中度至重度活动性溃疡性结肠炎患者中与疾病相关的治疗性蛋白质药物相互作用

Assessment of Disease-Related Therapeutic Protein Drug-Drug Interaction for Etrolizumab in Patients With Moderately to Severely Active Ulcerative Colitis.

作者信息

Wei Xiaohui, Kenny Jane R, Dickmann Leslie, Maciuca Romeo, Looney Caroline, Tang Meina T

机构信息

Clinical Pharmacology, Genentech, Inc, South San Francisco, CA, USA.

Drug Metabolism and Pharmacokinetics, Genentech, Inc, South San Francisco, CA, USA.

出版信息

J Clin Pharmacol. 2016 Jun;56(6):693-704. doi: 10.1002/jcph.649. Epub 2016 Jan 11.

Abstract

The efficacy and safety of etrolizumab, a humanized IgG1 mAb, were evaluated in patients with ulcerative colitis (UC) in a phase 2 study (EUCALYPTUS). The current study assessed the risk of therapeutic protein drug-drug interaction (TP-DDI) of etrolizumab on CYP3A activity in patients with UC. Literature review was performed to compare serum proinflammatory cytokine levels and pharmacokinetic (PK) parameters of CYP3A substrate drugs between patients with inflammatory bowel disease (IBD) and healthy subjects. Treatment effect of etrolizumab on CYP3A activity was evaluated by measuring colonic CYP3A4 mRNA expression and serum C-reactive protein (CRP) in EUCALYPTUS patients. Literature data suggested similar levels between IBD patients and healthy subjects for serum proinflammatory cytokines and PK parameters of CYP3A substrate drugs. Additionally, treatment with etrolizumab did not change colonic CYP3A4 mRNA expression or serum CRP levels in UC patients. In conclusion, our results indicate a low TP-DDI risk for etrolizumab in UC patients, particularly on medications metabolized by CYP3A.

摘要

在一项2期研究(EUCALYPTUS)中,对人源化IgG1单克隆抗体etrolizumab在溃疡性结肠炎(UC)患者中的疗效和安全性进行了评估。当前研究评估了etrolizumab在UC患者中对CYP3A活性的治疗性蛋白质药物-药物相互作用(TP-DDI)风险。进行文献综述以比较炎症性肠病(IBD)患者和健康受试者之间血清促炎细胞因子水平以及CYP3A底物药物的药代动力学(PK)参数。通过测量EUCALYPTUS患者的结肠CYP3A4 mRNA表达和血清C反应蛋白(CRP)来评估etrolizumab对CYP3A活性的治疗效果。文献数据表明,IBD患者和健康受试者之间血清促炎细胞因子水平以及CYP3A底物药物的PK参数相似。此外,etrolizumab治疗并未改变UC患者的结肠CYP3A4 mRNA表达或血清CRP水平。总之,我们的结果表明etrolizumab在UC患者中发生TP-DDI的风险较低,尤其是对由CYP3A代谢的药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/afa9/5066705/ad401eb920d7/JCPH-56-693-g001.jpg

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