Evolocumab for Early Reduction of LDL Cholesterol Levels in Patients With Acute Coronary Syndromes (EVOPACS)

被引:231
作者
Koskinas, Konstantinos C. [1 ]
Windecker, Stephan [1 ]
Pedrazzini, Giovanni [2 ]
Mueller, Christian [3 ]
Cook, Stephane [4 ]
Matter, Christian M. [5 ]
Mueller, Olivier [6 ]
Haner, Jonas [1 ]
Gencer, Baris [7 ]
Crljenica, Carmela [2 ]
Amini, Poorya [8 ]
Deckarm, Olga [1 ]
Iglesias, Juan F. [7 ]
Raber, Lorenz [1 ]
Heg, Dik [8 ]
Mach, Francois [7 ]
机构
[1] Univ Bern, Inselspital, Bern Univ Hosp, Dept Cardiol, CH-3010 Bern, Switzerland
[2] Cardiocentro, Lugano, Switzerland
[3] Univ Hosp Basel, Dept Cardiol, Basel, Switzerland
[4] Fribourg Hosp & Univ, Dept Cardiol, Fribourg, Switzerland
[5] Univ Hosp Zurich, Univ Heart Ctr, Dept Cardiol, Zurich, Switzerland
[6] Lausanne Univ Hosp, Serv Cardiol, Lausanne, Switzerland
[7] Geneva Univ Hosp, Dept Cardiol, Geneva, Switzerland
[8] Univ Bern, CTU Bern, Bern, Switzerland
关键词
acute coronary syndrome; evolocumab; LDL-C; PCSK9; inhibitor; DOUBLE-BLIND; AMG; 145; EFFICACY; STATIN; SAFETY; ATORVASTATIN; GUIDELINES; ANTIBODY; EVENTS;
D O I
10.1016/j.jacc.2019.08.010
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND Although guidelines recommend in-hospital initiation of high-intensity statin therapy in patients with acute coronary syndromes (ACS), low-density lipoprotein cholesterol (LDL-C) target levels are frequently not attained. Evolocumab, a rapidly acting, potent LDL-C-lowering drug, has not been studied in the acute phase of ACS. OBJECTIVES The purpose of this study was to assess the feasibility, safety, and LDL-C-lowering efficacy of evolocumab initiated during the in-hospital phase of ACS. METHODS The authors conducted an investigator-initiated, randomized, double-blind, placebo-controlled trial involving 308 patients hospitalized for ACS with elevated LDL-C levels ($1.8 mmol/l on high-intensity statin for at least 4 weeks; $2.3 mmol/l on low- or moderate-intensity statin; or $3.2 mmol/l on no stable dose of statin). Patients were randomly assigned 1:1 to receive subcutaneous evolocumab 420 mg or matching placebo, administered in-hospital and after 4 weeks, on top of atorvastatin 40 mg. The primary endpoint was percentage change in calculated LDL-C from baseline to 8 weeks. RESULTS Most patients (78.2%) had not been on previous statin treatment. Mean LDL-C levels decreased from 3.61 to 0.79 mmol/l at week 8 in the evolocumab group, and from 3.42 to 2.06 mmol/l in the placebo group; the difference in mean percentage change from baseline was similar to 40.7% (95% confidence interval: similar to 45.2 to similar to 36.2; p < 0.001). LDL-C levels <1.8 mmol/l were achieved at week 8 by 95.7% of patients in the evolocumab group versus 37.6% in the placebo group. Adverse events and centrally adjudicated cardiovascular events were similar in both groups. CONCLUSIONS In this first randomized trial assessing a PCSK9 antibody in the very high-risk setting of ACS, evolocumab added to high-intensity statin therapy was well tolerated and resulted in substantial reduction in LDL-C levels, rendering >95% of patients within currently recommended target levels. (EVOlocumab for Early Reduction of LDL-cholesterol Levels in Patients With Acute Coronary Syndromes [EVOPACS]; NCT03287609) (J Am Coll Cardiol 2019;74:2452-62) (c) 2019 by the American College of Cardiology Foundation.
引用
收藏
页码:2452 / 2462
页数:11
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