Final 5-Year Report of the Randomized BIO-RESORT Trial Comparing 3 Contemporary Drug-Eluting Stents in All-Comers

被引:24
作者
Ploumen, Eline H. [1 ,2 ]
Pinxterhuis, Tineke H. [1 ,2 ]
Buiten, Rosaly A. [1 ]
Zocca, Paolo [1 ]
Danse, Peter W. [3 ]
Schotborgh, Carl E. [4 ]
Scholte, Martijn [5 ]
Gin, R. Melvyn Tjon Joe [3 ]
Somi, Samer [4 ]
van Houwelingen, K. Gert [1 ]
Stoel, Martin G. [1 ]
de Man, H. A. F. [1 ]
Hartmann, Marc [1 ]
Linssen, Gerard C. M. [6 ]
van der Heijden, Liefke C. [1 ]
Kok, Marlies M. [1 ]
Doggen, Carine J. M. [2 ]
von Birgelen, Clemens [1 ,2 ]
机构
[1] Med Spectrum Twente, Thoraxctr Twente, Dept Cardiol, Koningspl 1, NL-7512 KZ Enschede, Netherlands
[2] Univ Twente, Tech Med Ctr, Dept Hlth Technol & Serv Res, Fac BMS, Enschede, Netherlands
[3] Rijnstate Hosp, Dept Cardiol, Arnhem, Netherlands
[4] Haga Hosp, Dept Cardiol, The Hague, Netherlands
[5] Albert Schweitzer Hosp, Dept Cardiol, Dordrecht, Netherlands
[6] Hosp Grp Twente, Dept Cardiol, Almelo, Hengelo, Netherlands
来源
JOURNAL OF THE AMERICAN HEART ASSOCIATION | 2022年 / 11卷 / 22期
关键词
biodegradable polymer; drug-eluting stent; durable polymer; percutaneous coronary intervention; randomized clinical trial; DURABLE-POLYMER; BIODEGRADABLE-POLYMER; THIN-STRUT; OUTCOMES; IMPLANTATION;
D O I
10.1161/JAHA.122.026041
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
BACKGROUND: In a previous trial, higher 5-year mortality was observed following treatment with biodegradable polymer Orsiro sirolimus-eluting stents (SES). We assessed 5-year safety and efficacy of all-comers as well as patients with diabetes treated with SES or Synergy everolimus-eluting stents (EES) versus durable polymer Resolute Integrity zotarolimus-eluting stents (ZES). METHODS AND RESULTS: The randomized BIO-RESORT (Comparison of Biodegradable Polymer and Durable Polymer DrugEluting Stents in an All Comers Population) trial enrolled 3514 all-comer patients at 4 Dutch cardiac centers. Patients aged >= 18years who required percutaneous coronary intervention were eligible. Participants were stratified for diabetes and randomized to treatment with SES, EES, or ZES (1:1:1). The main end point was target vessel failure (cardiac mortality, target vessel myocardial infarction, or target vessel revascularization). Five-year follow-up was available in 3183 of 3514 (90.6%) patients. The main end point target vessel failure occurred in 142 of 1169 (12.7%) patients treated with SES, 130 of 1172 (11.6%) treated with EES, versus 157 of 1173 (14.1%) treated with ZES (hazard ratio [HR], 0.89 [95% CI, 0.71-1.12], Plog-rank=0.31; and HR, 0.82 [95% CI, 0.65-1.04], Plog-rank=0.10, respectively). Individual components of target vessel failure showed no significant between-stent difference. Very late definite stent thrombosis rates were low and similar (SES, 1.1%; EES, 0.6%; ZES, 0.9%). In patients with diabetes, target vessel failure did not differ significantly between stent-groups (SES, 19.8%; EES, 19.2%; versus ZES, 21.1% [Plog-rank=0.69 and Plog-rank= 0.63]). CONCLUSIONS: Orsiro SES, Synergy EES, and Resolute Integrity ZES showed similar 5-year outcomes of safety and efficacy, including mortality. A prespecified stent comparison in patients with diabetes also revealed no significant differences in 5-year clinical outcomes.
引用
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页数:23
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