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Design and rationale for a randomised comparison of everolimus-eluting stents and coronary artery bypass graft surgery in selected patients with left main coronary artery disease: The EXCEL trial

  • Arie Pieter Kappetein
  • , Patrick W. Serruys
  • , Joseph F. Sabik
  • , Martin B. Leon
  • , David P. Taggart
  • , Marie Claude Morice
  • , Bernard J. Gersh
  • , Stuart J. Pocock
  • , David J. Cohen
  • , Lars Wallentin
  • , Ori Ben-Yehuda
  • , Gerrit Anne Van Es
  • , Charles A. Simonton
  • , Gregg W. Stone
  • Erasmus MC
  • Imperial College London
  • Cleveland Clinic Foundation
  • Columbia University Medical Center
  • John Radcliffe Hospital
  • Institut Hospitalier Jacques Cartier
  • Mayo Clinic College of Medicine and Science
  • London School of Hygiene and Tropical Medicine
  • Saint Luke's Mid America Heart Institute
  • Uppsala University
  • Cardialysis BV
  • Abbott Vascular

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

74 Citations (Scopus)

Abstract

Aims: Coronary artery bypass graft (CABG) surgery is the standard of care for revascularisation of patients with left main coronary artery disease (LMCAD). Recent studies have suggested that percutaneous coronary intervention (PCI) with drug-eluting stents (DES) may provide comparable outcomes in selected patients with LMCAD without extensive CAD. We therefore designed a trial to investigate whether PCI with XIENCE cobalt-chromium everolimus-eluting stents (CoCr-EES) would result in non-inferior or superior clinical outcomes to CABG in selected patients with LMCAD. Methods and results: The Evaluation of XIENCE versus Coronary Artery Bypass Surgery for Effectiveness of Left Main Revascularization (EXCEL) trial is a prospective, open-label, multicentre, international study of 1,900 randomised subjects. Patients with significant LMCAD with a SYNTAX score ≤32 and local Heart Team consensus that the subject is appropriate for revascularisation by both PCI and CABG are consented and randomised 1:1 to undergo PCI using CoCr-EES or CABG. All patients undergo follow-up for five years. The primary endpoint is the three-year composite rate of death, stroke or myocardial infarction, assessed at a median follow-up of at least three years (with at least two-year follow-up in all patients), powered for sequential non-inferiority and superiority testing. Conclusions: The EXCEL study will define the contemporary roles of CABG and PCI using XIENCE CoCr-EES in patients with LMCAD disease with low and intermediate SYNTAX scores.

Original languageEnglish
Pages (from-to)861-872
Number of pages12
JournalEuroIntervention
Volume12
Issue number7
DOIs
Publication statusPublished - Sep 2016
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Coronary bypass surgery
  • Drug-eluting stents
  • Left main disease
  • Randomised trial

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