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Adding evolocumab to existing lipid-lowering therapies significantly reduced first MACE risk, highlighting its efficacy in reducing cardiovascular mortality.
Adding evolocumab, a proprotein convertase subtilisin-kexin type 9 (PCSK9) inhibitor, to existing high-intensity cholesterol-lowering therapy reduces the risk of a first major cardiovascular event (MACE) among patients with atherosclerotic cardiovascular disease (ASCVD) or diabetes, according to data from the VESALIUS-CV trial.1
This late-breaking science presentation was given at the American Heart Association’s Scientific Sessions 2025 in New Orleans, Louisiana, by Erin Bohula, MD, assistant professor of medicine, Harvard Medical School, Brigham & Women’s Hospital, and colleagues. It encapsulated the topline results from VESALIUS-CV, an international, double-blind, randomized, placebo-controlled trial.1,2
“The results from the VESALIUS-CV trial represent the first demonstration of improved cardiovascular outcomes with a PCSK9 inhibitor, or any non-statin for that matter, in patients without a previous heart attack or stroke who are already being treated with a high-intensity lipid-lowering regimen,” Bohula said in a statement.1
VESALIUS-CV was conducted at 774 sites in 33 countries, including patients who were either 50-79 years (in men) or 55-79 years (in women) with an LDL cholesterol level of ≥90 mg/dL, a non-high-density lipoprotein (non-HDL) cholesterol level of ≥120 mg/dL, or an apolipoprotein B (ApoB) level of ≥80 mg/dL. Additionally, patients were required to have been receiving stable, optimized lipid-lowering therapy for ≥2 weeks prior to enrollment. Patients were excluded if they exhibited a history of myocardial infarction or stroke.2
In addition to these criteria, patients had to meet trial criteria for coronary artery disease, atherosclerotic cerebrovascular disease, peripheral artery disease, or high-risk diabetes. These patients had to have ≥1 additional criterion placing them at higher risk for cardiovascular disease, such as an age of ≥65 years, active smoking, severely elevated lipid levels, or concomitant ASCVD and diabetes.2
Bohula and colleagues randomly assigned patients in a 1:1 ratio to receive either subcutaneous evolocumab 140 mg every 2 weeks or matching placebo. The 2 primary efficacy endpoints of the study were a composite of death from coronary heart disease, myocardial infarction, or ischemic stroke (3-point MACE) and a composite of death from coronary heart disease, myocardial infarction, ischemic stroke, or ischemia-driven arterial revascularization (4-point MACE).2
Ultimately, a total of 12,257 patients were enrolled and randomized, with characteristics consistent between the 2 trial groups. Median age was 66 years (interquartile range, 60-71), and roughly 2/3 of patients met criteria for qualifying atherosclerosis, including 45% with coronary artery disease, 17% with peripheral artery disease, and 10% with cerebrovascular disease.2
Investigators found that evolocumab therapy led to substantially lower risks of both primary efficacy endpoints when compared to placebo. A 3-point MACE event occurred in 336 patients in the evolocumab group and 443 in the placebo arm (HR, 0.75; 95% CI, 0.65-0.86; P <.001), which corresponded to a 25% lower risk. A 4-point MACE event occurred in 747 patients in the evolocumab arm and 907 in the placebo arm (HR, 0.81; 95% CI, 0.73-0.89; P <.001), which translated to a 19% lower risk. Additionally, there was no evidence recorded of a between-group difference in adverse event incidence leading to discontinuation.2
“Together with data from genetic studies of PCSK9 variants and other PCSK9 inhibitor outcomes studies, our findings suggest that long-term lowering with PCSK9 inhibitors can help to improve cardiovascular morbidity and potentially mortality over time,” Bohula said. “The findings also support the use of intensive LDL-C lowering to achieve targets of around 40 mg/dL to help prevent a first major cardiovascular event.”1
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