Long-Term Safety and Efficacy of Platinum Chromium Everolimus-Eluting Stents in Coronary Artery Disease 5-Year Results From the PLATINUM Trial

被引:20
|
作者
Kelly, Christopher R. [1 ,2 ]
Teirstein, Paul S. [3 ]
Meredith, Ian T. [4 ]
Farah, Bruno [5 ]
Dubois, Christophe L. [6 ]
Feldman, Robert L. [7 ]
Dens, Joseph [8 ]
Hagiwara, Nobuhisa [9 ]
Rabinowitz, Abram [10 ]
Carrie, Didier [11 ]
Pompili, Vincent [12 ]
Bouchard, Alain [13 ]
Saito, Shigeru [14 ]
Allocco, Dominic J. [15 ]
Dawkins, Keith D. [15 ]
Stone, Gregg W. [1 ,2 ]
机构
[1] Columbia Univ, Med Ctr, New York Presbyterian Hosp, New York, NY 10019 USA
[2] Cardiovasc Res Fdn, New York, NY USA
[3] Scripps Clin, La Jolla, CA USA
[4] Monash Med Ctr, Southern Hlth, MonashHEART, Clayton, Vic, Australia
[5] Clin Pasteur Toulouse, Toulouse, France
[6] Univ Hosp Leuven, Leuven, Belgium
[7] Mediquest Res Munroe Reg Med Ctr, Ocala, FL USA
[8] Ziekenhuis Oost Limburg, Dept Cardiol, Genk, Belgium
[9] Tokyo Womens Med Univ Hosp, Shinjuku Ku, Tokyo, Japan
[10] TexSan Heart Hosp, San Antonio, TX USA
[11] Univ Paul Sabatier, CHU Rangueil, Toulouse, France
[12] Univ Nebraska Med Ctr, Omaha, NE USA
[13] Baptist Med Center Princeton, Birmingham, AL USA
[14] Shonan Kamakura Gen Hosp, Kanagawa, Japan
[15] Boston Sci Corp, Marlborough, MA USA
关键词
coronary artery disease; drug-eluting stent(s); percutaneous coronary intervention; stent design; RANDOMIZED-TRIAL; PROMUS ELEMENT; III TRIAL; MULTICENTER; LESIONS; SYSTEM; INTERVENTION; METAANALYSIS; THROMBOSIS; OUTCOMES;
D O I
10.1016/j.jcin.2017.06.070
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES The authors sought to evaluate the final 5-year safety and effectiveness of the platinum-chromium everolimus-eluting stent (PtCr-EES) in the randomized trial, as well as in 2 single-arm substudies that evaluated PtCr-EES in small vessels (diameter < 2.5 mm; n =94) and long lesions (24 to 34 mm; n = 102). BACKGROUND In the multicenter, randomized PLATINUM (PLATINUM Clinical Trial to Assess the PROMUS Element Stent System for Treatment of De Novo Coronary Artery Lesions), the PtCr-EES was noninferior to the cobalt-chromium everolimus-eluting stent (CoCr-EES) at 1 year in 1,530 patients undergoing percutaneous coronary intervention. METHODS Patients with 1 or 2 de novo coronary artery lesions (reference vessel diameter 2.50 to 4.25 mm, length # 24 mm) were randomized 1: 1 to PtCr-EES versus CoCr-EES. All patients in the substudies received PtCr-EES. The primary endpoint was target lesion failure (TLF), a composite of target vessel-related cardiac death, target vesselrelated myocardial infarction, or ischemia-driven target lesion revascularization. RESULTS In the randomized trial, the 5-year TLF rate was 9.1% for PtCr-EES and 9.3% for CoCr-EES (hazard ratio [HR]: 0.97; p = 0.87). Landmark analysis demonstrated similar TLF rates from discharge to 1 year (HR: 1.12; p = 0.70) and from 1 to 5 years (HR: 0.90; p = 0.63). There were no significant differences in the rates of cardiac death, myocardial infarction, target lesion or vessel revascularization, or stent thrombosis. PtCr-EES had 5-year TLF rates of 7.0% in small vessels and 13.6% in long lesions. CONCLUSIONS PtCr-EES demonstrated comparable safety and effectiveness to CoCr-EES through 5 years of follow-up, with low rates of stent thrombosis and other adverse events. The 5-year event rates were also acceptable in patients with small vessels and long lesions treated with PtCr-EES. (C) 2017 by the American College of Cardiology Foundation.
引用
收藏
页码:2392 / 2400
页数:9
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