Key result
1-month DAPT followed by 23-month ticagrelor monotherapy after bifurcation PCI did not significantly reduce all-cause death or new Q-wave MI compared to standard DAPT (HR 0.74; 95% CI 0.51-1.07).
Why the study?
The impact of ticagrelor monotherapy following 1-month DAPT after PCI for bifurcation lesions was unknown.
Does 1-month DAPT followed by 23-month ticagrelor monotherapy reduce all-cause death or new Q-wave MI in patients undergoing PCI for bifurcation lesions compared to standard 12-month DAPT?
RCT (n=15,845)
randomized
Does 1-month DAPT followed by 23-month ticagrelor monotherapy reduce all-cause death or new Q-wave MI in patients undergoing PCI for bifurcation lesions compared to standard 12-month DAPT?
Hazard Ratio: 0.74 (95% CI 0.51–1.07)
Ticagrelor monotherapy after 1 month of DAPT did not significantly reduce death or Q-wave MI compared to standard 12-month DAPT in patients undergoing PCI for bifurcation lesions, though it reduced stent thrombosis at the cost of increased stroke risk.
No benefit seen with ticagrelor monotherapy post-bifurcation PCI; hypothesis-generating and should not yet change practice.
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.
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Kogame et al. (2019) conducted an RCT in bifurcation lesions requiring percutaneous coronary intervention (n=15,845). 1-month DAPT followed by 23-month ticagrelor monotherapy vs. 12-month DAPT followed by 12-month aspirin monotherapy was evaluated on composite of all-cause death or new Q-wave myocardial infarction (MI) at 2 years (HR 0.74, 95% CI 0.51-1.07). 1-month DAPT followed by 23-month ticagrelor monotherapy after bifurcation PCI did not significantly reduce all-cause death or new Q-wave MI compared to standard DAPT (HR 0.74; 95% CI 0.51-1.07).
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