Alirocumab as Add-On to Atorvastatin Versus Other Lipid Treatment Strategies: ODYSSEY OPTIONS I Randomized Trial

被引:202
作者
Bays, Harold [1 ]
Gaudet, Daniel [2 ,3 ]
Weiss, Robert [4 ]
Ruiz, Juan Lima [5 ]
Watts, Gerald F. [6 ]
Gouni-Berthold, Ioanna [7 ]
Robinson, Jennifer [8 ]
Zhao, Jian [9 ]
Hanotin, Corinne [10 ]
Donahue, Stephen [9 ]
机构
[1] Louisville Metab & Atherosclerosis Res Ctr, Louisville, KY 40213 USA
[2] Univ Montreal, ECOGENE Clin Trial Ctr 21, Chicoutimi, PQ G7H 5H6, Canada
[3] Univ Montreal, Dept Med, Chicoutimi, PQ G7H 5H6, Canada
[4] Maine Res Associates, Auburn, ME 04210 USA
[5] Univ Hosp Vall dHebron, Lipid & Vasc Res Unit, Barcelona 8035, Spain
[6] Univ Western Australia, Lipid Disorders Clin, Ctr Cardiovasc Med, Royal Perth Hosp,Sch Med & Pharmacol, Perth, WA, Australia
[7] Univ Cologne, Ctr Endocrinol Diabet & Prevent Med, D-50923 Cologne, Germany
[8] Univ Iowa, Iowa City, IA 52242 USA
[9] Regeneron Pharmaceut Inc, Tarrytown, NY 10591 USA
[10] Sanofi, F-75014 Paris, France
关键词
DENSITY-LIPOPROTEIN CHOLESTEROL; MONOCLONAL-ANTIBODY; EFFICACY; HYPERCHOLESTEROLEMIA; EZETIMIBE; SAFETY; ROSUVASTATIN; PCSK9; THERAPY; DYSLIPIDEMIA;
D O I
10.1210/jc.2015-1520
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Context: Despite current standard of care, many patients at high risk of cardiovascular disease (CVD) still have elevated low-density lipoprotein cholesterol (LDL-C) levels. Alirocumab is a fully human monoclonal antibody inhibitor of proprotein convertase subtilisin/kexin type 9. Objective: The objective of the study was to compare the LDL-C-lowering efficacy of adding alirocumab vs other common lipid-lowering strategies. Design, Patients, and Interventions: Patients (n = 355) with very high CVD risk and LDL-C levels of 70 mg/dL or greater or high CVD risk and LDL-C of 100 mg/dL or greater on baseline atorvastatin 20 or 40 mg were randomized to one of the following: 1) add-on alirocumab 75 mg every 2 weeks (Q2W) sc; 2) add-on ezetimibe 10 mg/d; 3) double atorvastatin dose; or 4) for atorvastatin 40 mg regimen only, switch to rosuvastatin 40 mg. For patients not achieving protocol-defined LDL-C goals, the alirocumab dose was increased (blinded) at week 12 to 150 mg Q2W. Main Outcome Measure: The primary end point was percentage change in calculated LDL-C from baseline to 24 weeks (intent to treat). Results: Among atorvastatin 20 and 40 mg regimens, respectively, add-on alirocumab reduced LDL-C levels by 44.1% and 54.0% (P < .001 vs all comparators); add-on ezetimibe, 20.5% and 22.6%; doubling of atorvastatin dose, 5.0% and 4.8%; and switching atorvastatin 40 mg to rosuvastatin 40 mg, 21.4%. Most alirocumab-treated patients (87.2% and 84.6%) achieved their LDL-C goals. Most alirocumab-treated patients (86%) maintained their 75-mg Q2W regimen. Treatment-emergent adverse events occurred in 65.4% of alirocumab patients vs 64.4% ezetimibe and 63.8% double atorvastatin/switch to rosuvastatin (data were pooled). Conclusions: Adding alirocumab to atorvastatin provided significantly greater LDL-C reductions vs adding ezetimibe, doubling atorvastatin dose, or switching to rosuvastatin and enabled greater LDL-C goal achievement.
引用
收藏
页码:3140 / 3148
页数:9
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