Meta-Analysis of Everolimus-Eluting Versus Paclitaxel-Eluting Stents in Coronary Artery Disease

被引:161
作者
Dangas, George D. [1 ,2 ]
Serruys, Patrick W. [3 ]
Kereiakes, Dean J. [4 ]
Hermiller, James [5 ]
Rizvi, Ali [5 ]
Newman, William [6 ]
Sudhir, Krishnankutty [7 ]
Smith, Robert S., Jr. [7 ]
Cao, Sherry [7 ]
Theodoropoulos, Kleanthis [1 ,2 ]
Cutlip, Donald E. [8 ]
Lansky, Alexandra J. [9 ]
Stone, Gregg W. [2 ,10 ]
机构
[1] Mt Sinai Med Ctr, Div Cardiol, New York, NY 10022 USA
[2] Cardiovasc Res Fdn, New York, NY USA
[3] Cardialysis & Thoraxctr, Rotterdam, Netherlands
[4] Christ Hosp Heart & Vasc Ctr, Lindner Res Ctr, Cincinnati, OH USA
[5] Heart Ctr Indiana, Indianapolis, IN USA
[6] Wake Med Ctr, Div Cardiol, Raleigh, NC USA
[7] Abbott Vasc, Santa Clara, CA USA
[8] Harvard Clin Res Inst, Div Cardiol, Boston, MA USA
[9] Yale Univ, Med Ctr, Div Cardiol, New Haven, CT USA
[10] Columbia Univ, Med Ctr, New York Presbyterian Hosp, Div Cardiol, New York, NY USA
关键词
everolimus; paclitaxel; restenosis; RANDOMIZED CONTROLLED-TRIAL; MYOCARDIAL-INFARCTION; FOLLOW-UP; THROMBOSIS; RESTENOSIS; IMPACT;
D O I
10.1016/j.jcin.2013.05.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives This study sought to investigate whether the everolimus-eluting stent (EES) is superior to the paclitaxel-eluting stent (PES) with respect to long-term individual clinical outcomes. Background Individual studies have indicated a clinical advantage of coronary EES compared with PES with respect to restenosis and the composite endpoint of major adverse cardiac events. However, these trials were not powered for superiority in low-frequency event rates and have reported limited data beyond 1-year follow-up. Methods We conducted a meta-analysis of the final 3-year results from the international SPIRIT (Clinical Evaluation of the Xience V Everolimus Eluting Coronary Stent System in the Treatment of Patients With De Novo Native Coronary Artery Lesions) II, III, and IV clinical trials. Individual patient data from 4,989 patients who were prospectively randomized to treatment with EES (n = 3,350) or PES (n = 1,639) were pooled for analysis. Results At 3-year follow-up, EES was superior to PES in reducing the following event rates: target lesion failure (8.9% vs. 12.5%, hazard ratio [HR]: 0.71, 95% confidence interval [CI]: 0.59 to 0.85; p = 0.0002), all-cause mortality (3.2% vs 5.1%, HR: 0.65, 95% CI: 0.49 to 0.86; p = 0.003), myocardial infarction (3.2% vs. 5.1%, HR: 0.64, 95% CI: 0.48 to 0.85; p = 0.002), cardiac death or myocardial infarction (4.4% vs. 6.3%, HR: 0.70, 95% CI: 0.54 to 0.90; p = 0.005), ischemia-driven target lesion revascularization (6.0% vs. 8.2%, HR: 0.72, 95% CI: 0.58 to 0.90; p = 0.004), stent thrombosis (0.7% vs. 1.7%, HR: 0.45, 95% CI: 0.26 to 0.78; p = 0.003), and major adverse cardiac events (9.4% vs. 13.0%, HR: 0.71, 95% CI: 0.60 to 0.85; p = 0.0002). No interaction was present between stent type and the 3-year relative rates of target lesion failure across a broad range of subgroups, with the exception of diabetes and vessel (left anterior descending vs. other). Conclusions In this large dataset with 3-year follow-up, coronary implantation of EES compared with PES resulted in reduced rates of all-cause mortality, myocardial infarction, ischemia-driven target lesion revascularization, stent thrombosis, and target lesion failure. Further research is warranted to characterize possible interactions between stent type, diabetes, and vessel. (C) 2013 by the American College of Cardiology Foundation
引用
收藏
页码:914 / 922
页数:9
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