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Rationale and design of the effect of evolocumab in patients at high cardiovascular risk without prior myocardial infarction or stroke (VESALIUS-CV) trial

医学 Evolocumab公司 内科学 冲程(发动机) 心肌梗塞 心脏病学 临床终点 人口 PCSK9 随机对照试验 载脂蛋白B 胆固醇 脂蛋白 载脂蛋白A1 工程类 环境卫生 机械工程 低密度脂蛋白受体
作者
Erin A. Bohula,Nicholas Marston,Andrea Ruzza,Sabina A. Murphy,Gaetano Maria De Ferrari,Rafael Díaz,Lawrence A. Leiter,Mary Elliott‐Davey,Huei Wang,Ajay Bhatia,Robert P. Giugliano,Marc S. Sabatine
出处
期刊:American Heart Journal [Elsevier BV]
卷期号:269: 179-190 被引量:30
标识
DOI:10.1016/j.ahj.2023.12.004
摘要

The reduction of low-density lipoprotein cholesterol (LDL-C) with evolocumab, a fully human monoclonal antibody inhibitor of proprotein convertase subtilisin/kexin type 9 (PCSK9i), reduces the risk of major adverse cardiovascular events in patients with established atherosclerotic cardiovascular disease (ASCVD) with a prior MI, prior stroke, or symptomatic peripheral artery disease, with no offsetting safety concerns. The effect of evolocumab on CV outcomes in lower risk patients without a history of MI or stroke has not been explored.VESALIUS-CV is a randomized, double-blind, placebo-controlled, global clinical trial designed to evaluate the effect of evolocumab on the risk of major cardiovascular events in patients at high cardiovascular risk but without a prior ischemic event. The study population consists of 12,301 patients with atherosclerosis or high-risk diabetes mellitus without a prior MI or stroke; an LDL-C ≥90 mg/dL, or non-high-density lipoprotein cholesterol (non-HDL-C) ≥120 mg/dL, or apolipoprotein B ≥80 mg/dL; and treated with optimized lipid-lowering therapy. Patients were randomized in a 1:1 ratio to evolocumab 140mg subcutaneously every 2 weeks or matching placebo. The primary efficacy objective is to assess whether evolocumab reduces the risk of the dual primary composite endpoints of coronary heart disease (CHD) death, myocardial infarction (MI), or ischemic stroke (triple primary endpoint) and of CHD death, MI, ischemic stroke or ischemia-driven arterial revascularization (quadruple primary endpoint). Recruitment began in June 2019 and completed in November 2021. The trial is planned to continue until at least 751 patients experience an adjudicated triple endpoint, at least 1254 experience an adjudicated quadruple endpoint, and the median follow-up is ≥ 4.5 years.VESALIUS-CV will determine whether the addition of evolocumab to optimized lipid lowering therapy reduces cardiovascular events in patients at high cardiovascular risk without a prior MI or stroke.
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