5-Year Outcome Following Randomized Treatment of All-Comers With Zotarolimus-Eluting Resolute Integrity and Everolimus-Eluting PROMUS Element Coronary Stents Final Report of the DUTCH PEERS (TWENTE II) Trial

被引:44
|
作者
Zocca, Paolo [1 ]
Kok, Marlies M. [1 ]
Tandjung, Kenneth [1 ]
Danse, Peter W. [2 ]
Jessurun, Gillian A. J. [3 ]
Hautvast, Raymond W. M. [4 ]
van Houwelingen, K. Gert [1 ]
Stoel, Martin G. [1 ]
Schramm, Alexander R. [3 ]
Gin, R. Melvyn Tjon Joe [2 ]
de Man, Frits H. A. F. [1 ]
Hartmann, Marc [1 ]
Louwerenburg, J. W. [1 ]
Linssen, Gerard C. M. [5 ,6 ]
Lowik, Marije M. [1 ]
Doggen, Carine J. M. [7 ]
von Birgelen, Clemens [1 ,7 ]
机构
[1] Med Spectrum Twente, Thoraxctr Twente, Dept Cardiol, Enschede, Netherlands
[2] Rijnstate Hosp, Dept Cardiol, Arnhem, Netherlands
[3] Treant Zorggrp, Dept Cardiol, Location Scheper, Emmen, Netherlands
[4] Med Ctr Alkmaar, Dept Cardiol, Alkmaar, Netherlands
[5] Ziekenhuisgrp Twente, Dept Cardiol, Almelo, Netherlands
[6] Ziekenhuisgrp Twente, Dept Cardiol, Hengelo, Netherlands
[7] Univ Twente, MIRA Inst Biomed Technol & Tech Med, Dept Hlth Technol & Serv Res, Enschede, Netherlands
关键词
DES; long-term outcome; newer-generation drug-eluting stent(s); PCI; percutaneous coronary intervention; PROMUS Element everolimus-eluting stent(s); Resolute Integrity zotarolimus-eluting stent(s); BARE-METAL STENTS; NETWORK METAANALYSIS; THROMBOSIS; EFFICACY; MULTICENTER; SAFETY; SORT; VI;
D O I
10.1016/j.jcin.2017.11.031
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVES The study sought to evaluate for the first time the 5-year outcomes after treating an all-comers population with newer-generation cobalt chromium-based Resolute Integrity zotarolimus-eluting stents (ZES) (Medtronic, Santa Rosa, California) versus platinum chromium-based PROMUS Element everolimus eluting stents (EES) (Boston Scientific, Natick, Massachusetts). BACKGROUND The DUTCH PEERS (TWENTE II) (DUrable polymer-based sTent CHallenge of Promus ElemEnt versus ReSolute integrity: TWENTE II) trial is a randomized, multicenter, single-blinded, investigator-initiated all-comers trial that found at its main analysis similar 1-year safety and efficacy for both drug-eluting stents. It is the first randomized trial ever to investigate the Resolute Integrity ZES and the first trial to compare both devices. METHODS In total, 1,811 patients were 1: 1 randomized to ZES versus EES. We performed a pre-specified assessment of the 5-year clinical outcomes in terms of safety and efficacy. The main endpoint target vessel failure (TVF) is a composite of cardiac death, target vessel-related myocardial infarction, or target vessel revascularization. Secondary endpoints included the individual components of TVF, and stent thrombosis. The study was independently monitored, and adverse clinical events were independently adjudicated. RESULTS Five-year clinical follow-up data was available in 1,798 (99.3%) patients. The ZES and EES groups showed favorable outcomes, with similar 5-year incidence of TVF (13.2% vs. 14.2%; p(log-rank) = 0.62) and its individual components: cardiac death (4.5% vs. 4.9%; p(log-rank) = 0.69), target vessel-related myocardial infarction (3.1% vs. 2.6%; p(log-rank) = 0.47), and target vessel revascularization (7.6% vs. 8.6%; p(log-rank) = 0.46). The 5-year incidence of definite or probable stent thrombosis was similar (1.5% vs. 1.3%; p(log-rank) = 0.83). CONCLUSIONS At 5-year follow-up, the Resolute Integrity ZES and PROMUS Element EES showed similar and sustained results in terms of safety and efficacy for treating a broad population of all-comers. (c) 2018 The authors. Published by Elsevier on behalf of the American College of Cardiology Foundation. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
引用
收藏
页码:462 / 469
页数:8
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