2-Year Clinical Follow-Up From the Randomized Comparison of Biolimus-Eluting Stents With Biodegradable Polymer and Sirolimus-Eluting Stents With Durable Polymer in Routine Clinical Practice

被引:29
作者
Klauss, Volker [2 ]
Serruys, Patrick W. [5 ]
Pilgrim, Thomas [1 ]
Buszman, Pawel [11 ]
Linke, Axel [4 ]
Ischinger, Thomas [3 ]
Eberli, Franz [9 ]
Corti, Roberto [10 ]
Wijns, William [12 ]
Morice, Marie-Claude [13 ]
di Mario, Carlo [14 ]
van Geuns, Robert Jan [5 ]
van Es, Gerrit-Anne [6 ]
Kalesan, Bindu [1 ,7 ]
Wenaweser, Peter [1 ]
Jueni, Peter [7 ,8 ]
Windecker, Stephan [1 ,8 ]
机构
[1] Univ Hosp Bern, Dept Cardiol, CH-3010 Bern, Switzerland
[2] Univ Hosp Munich Innenstadt, Dept Cardiol, Munich, Germany
[3] Hosp Bogenhausen, Dept Cardiol, Munich, Germany
[4] Herzzentrum Leipzig, Leipzig, Germany
[5] Erasmus Univ, Thoraxctr, NL-3000 DR Rotterdam, Netherlands
[6] Cardialysis, Rotterdam, Netherlands
[7] Univ Bern, Inst Social & Prevent Med, Bern, Switzerland
[8] Univ Hosp Bern, Clin Trials Unit Bern, CH-3010 Bern, Switzerland
[9] Triemli Spiral, Dept Cardiol, Zurich, Switzerland
[10] Univ Hosp, Dept Cardiol, Zurich, Switzerland
[11] Med Univ Silesia, Dept Cardiol, Katowice, Poland
[12] Onze Lieve Vrouw Hosp, Dept Cardiol, Aalst, Belgium
[13] Inst Cardiovasc Paris Sud, Dept Cardiol, Paris, France
[14] Royal Brompton Hosp, Dept Cardiol, London SW3 6LY, England
关键词
restenosis; stems; thrombosis; CORONARY-ARTERY-DISEASE; BARE-METAL STENTS; OFF-LABEL; CLOPIDOGREL USE; DRUG; THROMBOSIS; OUTCOMES; IMPLANTATION; TRIAL; REVASCULARIZATION;
D O I
10.1016/j.jcin.2011.03.017
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives This study sought to investigate safety and efficacy of biolimus-eluting stents (BES) with biodegradable polymer as compared with sirolimus-eluting stents (SES) with durable polymer through 2 years of follow-up. Background BES with a biodegradable polymer provide similar efficacy and safety as SES with a durable polymer at 9 months. Clinical outcomes beyond the period of biodegradation of the polymer used for drug release and after discontinuation of dual antiplatelet therapy are of particular interest. Methods A total of 1,707 patients were randomized to unrestricted use of BES (n = 857) or SES (n = 850) in an all-comers patient population. Results At 2 years, BES remained noninferior compared with SES for the primary endpoint, which was a composite of cardiac death, myocardial infarction, or clinically indicated target vessel revascularization (BES 12.8% vs. SES 15.2%, hazard ratio [HR]: 0.84, 95% confidence interval [CI]: 0.65 to 1.08, P(noninferiority) < 0.0001, p(superiority =) 0.18). Rates of cardiac death (3.2% vs. 3.9%, HR: 0.81, 95% CI: 0.49 to 1.35, p = 0.42), myocardial infarction (6.3% vs. 5.6%, HR: 1.12, 95% CI: 0.76 to 1.65, p = 0.56), and clinically indicated target vessel revascularization (7.5% vs. 8.6%, HR: 0.86, 95% CI: 0.62 to 1.20, p = 0.38) were similar for BES and SES. The rate of definite stent thrombosis through 2 years was 2.2% for BES and 2.5% for SES (p = 0.73). For the period between 1 and 2 years, event rates for definite stent thrombosis were 0.2% for BES and 0.5% for SES (p = 0.42). After discontinuation of dual antiplatelet therapy, no very late definite stent thrombosis occurred in the BES group. Conclusions At 2 years of follow-up, the unrestricted use of BES with a biodegradable polymer maintained a similar safety and efficacy profile as SES with a durable polymer. (Limus Eluted From a Durable Versus Erodable Stent Coating [LEADERS]; NCT00389220) (J Am Coll Cardiol Intv 2011;4: 887-95) (C) 2011 by the American College of Cardiology Foundation
引用
收藏
页码:887 / 895
页数:9
相关论文
共 27 条
  • [1] Outcomes and complications associated with off-label and untested use of drug-eluting stents
    Beohar, Nirat
    Davidson, Charles J.
    Kip, Kevin E.
    Goodreau, Lynne
    Aslanidou Vlachos, Helen
    Meyers, Sheridan N.
    Benzuly, Keith H.
    Flaherty, James D.
    Ricciardi, Mark J.
    Bennett, Charles L.
    Williams, David O.
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2007, 297 (18): : 1992 - 2000
  • [2] Stent thrombosis late after implantation of first-generation drug-eluting stents - A cause for concern
    Camenzind, Edoardo
    Steg, P. Gabriel
    Wijns, William
    [J]. CIRCULATION, 2007, 115 (11) : 1440 - 1455
  • [3] Correlation of Intravascular Ultrasound Findings With Histopathological Analysis of Thrombus Aspirates in Patients With Very Late Drug-Eluting Stent Thrombosis
    Cook, Stephane
    Ladich, Elena
    Nakazawa, Gaku
    Eshtehardi, Parham
    Neidhart, Michel
    Vogel, Rolf
    Togni, Mario
    Wenaweser, Peter
    Billinger, Michael
    Seiler, Christian
    Gay, Steffen
    Meier, Bernhard
    Pichler, Werner J.
    Jueni, Peter
    Virmani, Renu
    Windecker, Stephan
    [J]. CIRCULATION, 2009, 120 (05) : 391 - 399
  • [4] Clinical end points in coronary stent trials - A case for standardized definitions
    Cutlip, Donald E.
    Windecker, Stephan
    Mehran, Roxana
    Boam, Ashley
    Cohen, David J.
    van Es, Gerrit-Anne
    Steg, P. Gabriel
    Morel, Marie-angele
    Mauri, Laura
    Vranckx, Pascal
    McFadden, Eugene
    Lansky, Alexandra
    Hamon, Martial
    Krucoff, Mitchell W.
    Serruys, Patrick W.
    [J]. CIRCULATION, 2007, 115 (17) : 2344 - 2351
  • [5] Clopidogrel use and long-term clinical outcomes after drug-eluting stent implantation
    Eisenstein, Eric L.
    Anstrom, Kevin J.
    Kong, David F.
    Shaw, Linda K.
    Tuttle, Robert H.
    Mark, Daniel B.
    Kramer, Judith M.
    Harrington, Robert A.
    Matchar, David B.
    Kandzari, David E.
    Peterson, Eric D.
    Schulman, Kevin A.
    Califf, Robert M.
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2007, 297 (02): : 159 - 168
  • [6] BioMatrix® Biolimus A9®-eluting coronary stent:: a next-generation drug-eluting stent for coronary artery disease
    Grube, Eberhard
    Buellesfeld, Lutz
    [J]. EXPERT REVIEW OF MEDICAL DEVICES, 2006, 3 (06) : 731 - 741
  • [7] Incremental cost-effectiveness of drug-eluting stents compared with a third-generation bare-metal stent in a real-world setting: randomised Basel Stent Kosten Effektivitats Trial (BASKET)
    Kaiser, C
    Brunner-LaRocca, HP
    Buser, PT
    Bonetti, PO
    Osswald, S
    Linka, A
    Bernheim, A
    Zutter, A
    Zellweger, M
    Grize, L
    Pfisterer, ME
    [J]. LANCET, 2005, 366 (9489) : 921 - 929
  • [8] Second-generation everolimus-eluting and paclitaxel-eluting stents in real-life practice (COMPARE): a randomised trial
    Kedhi, Elvin
    Joesoef, Kaiyum Sheik
    McFadden, Eugene
    Wassing, Jochem
    van Mieghem, Carlos
    Goedhart, Dick
    Smits, Pieter Cornelis
    [J]. LANCET, 2010, 375 (9710) : 201 - 209
  • [9] Long-term outcomes with drug-eluting stents versus bare-metal stents in Sweden
    Lagerqvist, Bo
    James, Stefan K.
    Stenestrand, Ulf
    Lindback, Johan
    Nilsson, Tage
    Wallentin, Lars
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2007, 356 (10) : 1009 - 1019
  • [10] A Randomized Comparison of the Endeavor Zotarolimus-Eluting Stent Versus the TAXUS Paclitaxel-Eluting Stent in De Novo Native Coronary Lesions 12-Month Outcomes From the ENDEAVOR IV Trial
    Leon, Martin B.
    Mauri, Laura
    Popma, Jeffrey J.
    Cutlip, Donald E.
    Nikolsky, Eugenia
    O'Shaughnessy, Charles
    Overlie, Paul A.
    McLaurin, Brent T.
    Solomon, Stuart L.
    Douglas, John S., Jr.
    Ball, Michael W.
    Caputo, Ronald P.
    Jain, Ash
    Tolleson, Thaddeus R.
    Reen, Bernard M., III
    Kirtane, Ajay J.
    Fitzgerald, Peter J.
    Thompson, Kweli
    Kandzari, David E.
    [J]. JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2010, 55 (06) : 543 - 554