TY - JOUR
T1 - Impact of Ticagrelor Monotherapy on Two-Year Clinical Outcomes in Patients with Long Stenting
T2 - A Post Hoc Analysis of the Global Leaders Trial
AU - Takahashi, Kuniaki
AU - Chichareon, Ply
AU - Modolo, Rodrigo
AU - Kogame, Norihiro
AU - Chang, Chun Chin
AU - Tomaniak, Mariusz
AU - Moschovitis, Aris
AU - Curzen, Nick
AU - Haude, Michael
AU - Jung, Werner
AU - Holmvang, Lene
AU - Garg, Scot
AU - Tijssen, Jan G P
AU - Wykrzykowska, Joanna J
AU - de Winter, Robbert J
AU - Hamm, Christian
AU - Steg, Philippe Gabriel
AU - Stoll, Hans-Peter
AU - Onuma, Yoshinobu
AU - Valgimigli, Marco
AU - Vranckx, Pascal
AU - Windecker, Stephan
AU - Serruys, Patrick W
PY - 2020/10/23
Y1 - 2020/10/23
N2 - AIMS: The aim of this study was to evaluate the impact of a novel antiplatelet regimen in patients with increasing total stent length (TSL). METHODS AND RESULTS: This is a post hoc analysis of the GLOBAL LEADERS trial, a prospective, multicentre, open-label, randomised trial, investigating the impact of the experimental strategy (one-month dual antiplatelet therapy [DAPT] followed by 23-month ticagrelor monotherapy) versus the reference regimen (12-month DAPT followed by 12-month aspirin monotherapy) in patients with a Biolimus A9-eluting stent (BES). The primary endpoint was the composite of all-cause death and new Q-wave myocardial infarction (MI), and the secondary endpoint was Bleeding Academic Research Consortium (BARC) type 3 or 5 bleeding at two years. To investigate the association between total stent length and outcomes, groups were compared in quartiles according to TSL; the fourth quartile group was at significantly higher ischaemic risk at two years. In that stratum (TSL ≥46 mm), the experimental strategy significantly reduced the risk of the primary endpoint (hazard ratio [HR] 0.67, 95% confidence interval [CI]: 0.49-0.90; pinteraction=0.043), while demonstrating a similar risk of BARC type 3 or 5 bleeding (HR 0.99, 95% CI: 0.66-1.49; pinteraction=0.975). CONCLUSIONS: Ticagrelor monotherapy could potentially balance ischaemic and bleeding risks, thereby achieving a net clinical benefit in patients with a TSL ≥46 mm with a BES.
AB - AIMS: The aim of this study was to evaluate the impact of a novel antiplatelet regimen in patients with increasing total stent length (TSL). METHODS AND RESULTS: This is a post hoc analysis of the GLOBAL LEADERS trial, a prospective, multicentre, open-label, randomised trial, investigating the impact of the experimental strategy (one-month dual antiplatelet therapy [DAPT] followed by 23-month ticagrelor monotherapy) versus the reference regimen (12-month DAPT followed by 12-month aspirin monotherapy) in patients with a Biolimus A9-eluting stent (BES). The primary endpoint was the composite of all-cause death and new Q-wave myocardial infarction (MI), and the secondary endpoint was Bleeding Academic Research Consortium (BARC) type 3 or 5 bleeding at two years. To investigate the association between total stent length and outcomes, groups were compared in quartiles according to TSL; the fourth quartile group was at significantly higher ischaemic risk at two years. In that stratum (TSL ≥46 mm), the experimental strategy significantly reduced the risk of the primary endpoint (hazard ratio [HR] 0.67, 95% confidence interval [CI]: 0.49-0.90; pinteraction=0.043), while demonstrating a similar risk of BARC type 3 or 5 bleeding (HR 0.99, 95% CI: 0.66-1.49; pinteraction=0.975). CONCLUSIONS: Ticagrelor monotherapy could potentially balance ischaemic and bleeding risks, thereby achieving a net clinical benefit in patients with a TSL ≥46 mm with a BES.
KW - Drug Therapy, Combination
KW - Drug-Eluting Stents
KW - Humans
KW - Percutaneous Coronary Intervention
KW - Platelet Aggregation Inhibitors/therapeutic use
KW - Prospective Studies
KW - Stents
KW - Ticagrelor/therapeutic use
KW - Treatment Outcome
UR - http://www.scopus.com/inward/record.url?scp=85094685012&partnerID=8YFLogxK
U2 - 10.4244/EIJ-D-19-00498
DO - 10.4244/EIJ-D-19-00498
M3 - Journal article
C2 - 31498113
SN - 1774-024X
VL - 16
SP - 634
EP - 644
JO - EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology
JF - EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology
IS - 8
ER -