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

  • Volker Klauss
  • , Patrick W. Serruys
  • , Thomas Pilgrim
  • , Pawel Buszman
  • , Axel Linke
  • , Thomas Ischinger
  • , Franz Eberli
  • , Roberto Corti
  • , William Wijns
  • , Marie Claude Morice
  • , Carlo Di Mario
  • , Robert Jan Van Geuns
  • , Gerrit Anne Van Es
  • , Bindu Kalesan
  • , Peter Wenaweser
  • , Peter Jni
  • , Stephan Windecker

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

30 Citations (Scopus)

Abstract

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)

Original languageEnglish
Pages (from-to)887-895
Number of pages9
JournalJACC: Cardiovascular Interventions
Volume4
Issue number8
DOIs
Publication statusPublished - Aug 2011
Externally publishedYes

Keywords

  • restenosis
  • stents
  • thrombosis

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