Clinical relevance of ticagrelor monotherapy following 1-month dual antiplatelet therapy after bifurcation percutaneous coronary intervention: Insight from GLOBAL LEADERS trial.


Journal

Catheterization and cardiovascular interventions : official journal of the Society for Cardiac Angiography & Interventions
ISSN: 1522-726X
Titre abrégé: Catheter Cardiovasc Interv
Pays: United States
ID NLM: 100884139

Informations de publication

Date de publication:
07 2020
Historique:
received: 11 05 2019
revised: 10 07 2019
accepted: 27 07 2019
pubmed: 15 8 2019
medline: 9 2 2021
entrez: 15 8 2019
Statut: ppublish

Résumé

The aim of this study was to investigate the impact of ticagrelor monotherapy following 1-month dual antiplatelet therapy (DAPT) after percutaneous coronary intervention (PCI) for bifurcation lesions. GLOBAL LEADERS was a randomized, superiority, all-comers trial comparing 1-month DAPT with ticagrelor and aspirin followed by 23-month ticagrelor monotherapy (experimental treatment) with standard 12-month DAPT followed by 12-month aspirin monotherapy (reference treatment) in patients treated with a biolimus A9-eluting stent. The primary endpoint was a composite of all-cause death or new Q-wave myocardial infarction (MI) at 2 years. Among the 15,845 patients included in this subgroup analysis, 2,498 patients (15.8%) underwent PCI for at least one bifurcation lesion. The incidence of the primary endpoint was similar between the bifurcation and nonbifurcation groups (4.7 vs. 4.0%, p = .083). The experimental treatment had no significant effect on the primary endpoint according to the presence/absence of a bifurcation lesion (bifurcation: hazard ratio [HR]: 0.74, 95% confidence interval [CI]: 0.51-1.07; nonbifurcation: HR: 0.90, 95% CI: 0.76-1.07, p for interaction = .343), but was associated with significant reduction in definite or probable stent thrombosis (p for interaction = .022) and significant excess of stroke (p for interaction = .018) when compared with the reference treatment. After PCI for bifurcation lesions using 1-month of DAPT followed by ticagrelor monotherapy for 23 months did not demonstrate explicit benefit regarding all-cause death or new Q-wave MI as in the overall trial.

Sections du résumé

BACKGROUND
The aim of this study was to investigate the impact of ticagrelor monotherapy following 1-month dual antiplatelet therapy (DAPT) after percutaneous coronary intervention (PCI) for bifurcation lesions.
METHODS
GLOBAL LEADERS was a randomized, superiority, all-comers trial comparing 1-month DAPT with ticagrelor and aspirin followed by 23-month ticagrelor monotherapy (experimental treatment) with standard 12-month DAPT followed by 12-month aspirin monotherapy (reference treatment) in patients treated with a biolimus A9-eluting stent. The primary endpoint was a composite of all-cause death or new Q-wave myocardial infarction (MI) at 2 years.
RESULTS
Among the 15,845 patients included in this subgroup analysis, 2,498 patients (15.8%) underwent PCI for at least one bifurcation lesion. The incidence of the primary endpoint was similar between the bifurcation and nonbifurcation groups (4.7 vs. 4.0%, p = .083). The experimental treatment had no significant effect on the primary endpoint according to the presence/absence of a bifurcation lesion (bifurcation: hazard ratio [HR]: 0.74, 95% confidence interval [CI]: 0.51-1.07; nonbifurcation: HR: 0.90, 95% CI: 0.76-1.07, p for interaction = .343), but was associated with significant reduction in definite or probable stent thrombosis (p for interaction = .022) and significant excess of stroke (p for interaction = .018) when compared with the reference treatment.
CONCLUSIONS
After PCI for bifurcation lesions using 1-month of DAPT followed by ticagrelor monotherapy for 23 months did not demonstrate explicit benefit regarding all-cause death or new Q-wave MI as in the overall trial.

Identifiants

pubmed: 31410968
doi: 10.1002/ccd.28428
doi:

Substances chimiques

Platelet Aggregation Inhibitors 0
Purinergic P2Y Receptor Antagonists 0
Ticagrelor GLH0314RVC

Types de publication

Comparative Study Equivalence Trial Journal Article Multicenter Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

100-111

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2019 Wiley Periodicals, Inc.

Références

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Auteurs

Norihiro Kogame (N)

Department of Cardiology, Amsterdam University Medical Center, Amsterdam, The Netherlands.
Department of Cardiology, Toho University medical center Ohashi hospital, Tokyo, Japan.

Ply Chichareon (P)

Department of Cardiology, Amsterdam University Medical Center, Amsterdam, The Netherlands.
Faculty of Medicine, Division of Cardiology, Department of Internal Medicine, Prince of Songkla University, Songkhla, Thailand.

Kenneth De Wilder (K)

Heart Centre, Imelda Hospital Bonheiden, Bonheiden, Belgium.

Kuniaki Takahashi (K)

Department of Cardiology, Amsterdam University Medical Center, Amsterdam, The Netherlands.

Rodrigo Modolo (R)

Department of Cardiology, Amsterdam University Medical Center, Amsterdam, The Netherlands.
Cardiology Division, Department of Internal Medicine, University of Campinas (UNICAMP), Campinas, Brazil.

Chun Chin Chang (CC)

Department of Interventional Cardiology, Thoraxcenter, Erasmus Medical Center, Rotterdam, The Netherlands.

Mariusz Tomaniak (M)

Department of Interventional Cardiology, Thoraxcenter, Erasmus Medical Center, Rotterdam, The Netherlands.

Hidenori Komiyama (H)

Department of Cardiology, Amsterdam University Medical Center, Amsterdam, The Netherlands.

Alaide Chieffo (A)

Interventional Cardiology Unit, IRCCS San Raffaele Scientific Institute, Milan, Italy.

Antonio Colombo (A)

Interventional Cardiology Unit, Villa Maria Cecila Hospital GVM, Cotignola (RA), Italy.

Scot Garg (S)

Department of Cardiology, Royal Blackburn Hospital, Blackburn, UK.

Yves Louvard (Y)

Department of Cardiology, Ramsay Générale de Santé, Institut Cardiovasculaire Paris Sud, Hopital Privé Jacques Cartier, Massy, France.

Peter Jüni (P)

Applied Health Research Centre, Li Ka Shing Knowledge Institute of St Michael's Hospital, Toronto, Ontario, Canada.
Department of Medicine and Institute of Health Policy, Management and Evaluation, University of Toronto, Toronto, Ontario, Canada.

Philippe G Steg (P)

French Alliance for Cardiovascular Trials (FACT), Université Paris-Diderot, Paris, France.

Christian Hamm (C)

Kerckhoff Heart and Thorax Center, University of Giessen, Giessen, Germany.

Pascal Vranckx (P)

Faculty of Medicine and Life Sciences, Jessa Ziekenhuis, the Hasselt University, Hasselt, Belgium.

Marco Valgimigli (M)

Department of Cardiology, Inselspital, University of Bern, Bern, Switzerland.

Stephan Windecker (S)

Department of Cardiology, Inselspital, University of Bern, Bern, Switzerland.

Hans-Peter Stoll (HP)

Biosensors Clinical Research, Morges, Switzerland.

Yoshinobu Onuma (Y)

Department of Interventional Cardiology, Thoraxcenter, Erasmus Medical Center, Rotterdam, The Netherlands.

Luc Janssens (L)

Heart Centre, Imelda Hospital Bonheiden, Bonheiden, Belgium.

Patrick W Serruys (PW)

International Centre for Circulatory Health, Imperial College London, London, UK.

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