Key result
Ticagrelor monotherapy after <1 month of DAPT was noninferior and superior to 12-month DAPT for death, MI, stent thrombosis, stroke, and major bleeding (HR 0.54; 95% CI 0.37-0.80; P=0.002).
Why the study?
Stopping aspirin within 1 month after drug-eluting stent implantation for ticagrelor monotherapy had not been exclusively evaluated in patients with acute coronary syndrome.
Does ticagrelor monotherapy after <1 month of DAPT improve net clinical benefit compared to 12 months of ticagrelor-based DAPT in patients with acute coronary syndrome undergoing drug-eluting stent implantation?
RCT (n=2,850)
Open-label
1:1
Yes
Does ticagrelor monotherapy after <1 month of DAPT improve net clinical benefit compared to 12 months of ticagrelor-based DAPT in patients with acute coronary syndrome undergoing drug-eluting stent implantation?
Hazard Ratio: 0.54 (95% CI 0.37–0.8)
Absolute Event Rate: 2.8% vs 5.2%
p-value: p=<0.001 for noninferiority; P=0.002 for superiority
Supports ticagrelor monotherapy after brief DAPT in ACS post-DES; extends randomized evidence for abbreviated dual therapy.
BACKGROUND: Stopping aspirin within 1 month after implantation of a drug-eluting stent for ticagrelor monotherapy has not been exclusively evaluated for patients with acute coronary syndrome. The aim of this study was to investigate whether ticagrelor monotherapy after <1 month of dual antiplatelet therapy (DAPT) is noninferior to 12 months of ticagrelor-based DAPT for adverse cardiovascular and bleeding events in patients with acute coronary syndrome. METHODS: In this randomized, open-label, noninferiority trial, 2850 patients with acute coronary syndrome who underwent drug-eluting stent implantation at 24 centers in South Korea were randomly assigned (1:1) to receive either ticagrelor monotherapy (90 mg twice daily) after <1 month of DAPT (n=1426) or 12 months of ticagrelor-based DAPT (n=1424) between April 24, 2019, and May 31, 2022. The primary end point was the net clinical benefit as a composite of all-cause death, myocardial infarction, definite or probable stent thrombosis, stroke, and major bleeding at 1 year after the index procedure in the intention-to-treat population. Key secondary end points were the individual components of the primary end point. RESULTS: Among 2850 patients who were randomized (mean age, 61 years; 40% ST-segment–elevation myocardial infarction), 2823 (99.0%) completed the trial. Aspirin was discontinued at a median of 16 days (interquartile range, 12–25 days) in the group receiving ticagrelor monotherapy after <1 month of DAPT. The primary end point occurred in 40 patients (2.8%) in the group receiving ticagrelor monotherapy after <1-month DAPT, and in 73 patients (5.2%) in the ticagrelor-based 12-month DAPT group (hazard ratio, 0.54 [95% CI, 0.37–0.80]; P <0.001 for noninferiority; P =0.002 for superiority). This finding was consistent in the per-protocol population as a sensitivity analysis. The occurrence of major bleeding was significantly lower in the ticagrelor monotherapy after <1-month DAPT group compared with the 12-month DAPT group (1.2% versus 3.4%; hazard ratio, 0.35 [95% CI, 0.20–0.61]; P <0.001). CONCLUSIONS: This study provides evidence that stopping aspirin within 1 month for ticagrelor monotherapy is both noninferior and superior to 12-month DAPT for the 1-year composite outcome of death, myocardial infarction, stent thrombosis, stroke, and major bleeding, primarily because of a significant reduction in major bleeding, among patients with acute coronary syndrome receiving drug-eluting stent implantation. Low event rates, which may suggest enrollment of relatively non–high-risk patients, should be considered in interpreting the trial. REGISTRATION: URL: https://www.clinicaltrials.gov ; Unique identifier: NCT03797651.
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Hong et al. (2023) conducted an RCT in Acute coronary syndrome (n=2,850). Ticagrelor monotherapy after <1 month of DAPT vs. 12 months of ticagrelor-based DAPT was evaluated on Net clinical benefit as a composite of all-cause death, myocardial infarction, definite or probable stent thrombosis, stroke, and major bleeding at 1 year (HR 0.54, 95% CI 0.37-0.80, p=<0.001 for noninferiority; P=0.002 for superiority). Ticagrelor monotherapy after <1 month of DAPT was noninferior and superior to 12-month DAPT for death, MI, stent thrombosis, stroke, and major bleeding (HR 0.54; 95% CI 0.37-0.80; P=0.002).
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