Long-term efficacy and safety of moderate-intensity statin with ezetimibe combination therapy versus high-intensity statin monotherapy in patients with atherosclerotic cardiovascular disease (RACING): a randomised, open-label, non-inferiority trial

被引:233
作者
Kim, Byeong-Keuk [1 ]
Hong, Sung-Jin [1 ]
Lee, Yong-Joon [1 ]
Hong, Soon Jun [2 ]
Yun, Kyeong Ho [3 ]
Hong, Bum-Kee [4 ]
Heo, Jung Ho [5 ]
Rha, Seung-Woon [6 ]
Cho, Yun-Hyeong [7 ]
Lee, Seung-Jun [1 ]
Ahn, Chul-Min [1 ]
Kim, Jung-Sun [1 ]
Ko, Young-Guk [1 ]
Choi, Donghoon [1 ]
Jang, Yangsoo [8 ]
Hong, Myeong-Ki [1 ]
机构
[1] Yonsei Univ, Severance Hosp, Div Cardiol, Coll Med, Seoul 03722, South Korea
[2] Korea Univ, Coll Med, Seoul, South Korea
[3] Wonkwang Univ Hosp, Iksan, South Korea
[4] Gangnam Severance Hosp, Seoul, South Korea
[5] Kosin Univ, Coll Med, Busan, South Korea
[6] Korea Univ, Guro Hosp, Seoul, South Korea
[7] Myongji Hosp, Goyang, South Korea
[8] CHA Univ, Dept Cardiol, CHA Bundang Med Ctr, Coll Med, Seongnam, South Korea
关键词
CHOLESTEROL-LOWERING TREATMENT; PLAQUE REGRESSION; LDL CHOLESTEROL; END-POINTS; METAANALYSIS; EVENTS; PARTICIPANTS; DEFINITIONS; ABSORPTION;
D O I
10.1016/S0140-6736(22)00916-3
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Drug combinations rather than increasing doses of one drug can achieve greater efficacy and lower risks. Thus, as an alternative to high-intensity statin monotherapy, moderate-intensity statin with ezetimibe combination therapy can lower LDL cholesterol concentrations effectively while reducing adverse effects. However, evidence from randomised trials to compare long-term clinical outcomes is needed. Methods In this randomised, open-label, non-inferiority trial, patients with atherosclerotic cardiovascular disease (ASCVD) at 26 clinical centres in South Korea were randomly assigned (1:1) to receive either moderate-intensity statin with ezetimibe combination therapy (rosuvastatin 10 mg with ezetimibe 10 mg) or high-intensity statin monotherapy (rosuvastatin 20 mg). The primary endpoint was the 3-year composite of cardiovascular death, major cardiovascular events, or non-fatal stroke, in the intention-to-treat population with a non-inferiority margin of 2.0%. This trial is registered with ClinicalTrials.gov, NCT03044665 and is complete. Findings Between Feb 14, 2017, and Dec 18, 2018, 3780 patients were enrolled: 1894 patients to the combination therapy group and 1886 to the high-intensity statin monotherapy group. The primary endpoint occurred in 172 patients (9.1%) in the combination therapy group and 186 patients (9.9%) in the high-intensity statin monotherapy group (absolute difference -0.78%; 90% CI -2.39 to 0.83). LDL cholesterol concentrations of less than 70 mg/dL at 1, 2, and 3 years were observed in 73%, 75%, and 72% of patients in the combination therapy group, and 55%, 60%, and 58% of patients in the high-intensity statin monotherapy group (all p<0.0001). Discontinuation or dose reduction of the study drug by intolerance was observed in 88 patients (4.8%) and 150 patients (8.2%), respectively (p<0.0001). Interpretation Among patients with ASCVD, moderate-intensity statin with ezetimibe combination therapy was non-inferior to high-intensity statin monotherapy for the 3-year composite outcomes with a higher proportion of patients with LDL cholesterol concentrations of less than 70 mg/dL and lower intolerance-related drug discontinuation or dose reduction. Copyright (c) 2022 Elsevier Ltd. All rights reserved.
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收藏
页码:380 / 390
页数:11
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