TALOS AMI Trial 2021

 Patients having PCI for acute MI who had completed one month of DAPT with aspirin and ticagrelor without ischemic or bleeding events were randomly assigned to either continue that regimen or switch to aspirin plus clopidogrel for the next 11 months in this study.



According to the findings of this trial, among patients undergoing PCI for AMI who had completed 1 month of DAPT with aspirin and ticagrelor without incident, switching to aspirin + clopidogrel for the next 11 months met criteria for noninferiority and superiority compared to continuing with aspirin + ticagrelor.


This was mostly due to a decrease in significant bleeding, although ischemia episodes were also reduced quantitatively with a de-escalation technique.


De-escalation was carried out without the need for genotype testing or reload.


These are intriguing findings that are both therapeutically meaningful and cost-effective. The only limitation is that this trial only involved East Asian patients, therefore its applicability in the United States is unknown.


In the last few years, we've seen a number of intriguing studies in the DAPT space.


The TWILIGHT trial has indicated that it may be possible to continue ticagrelor monotherapy and discontinue aspirin after 3 months with no reduction in ischemic outcomes and a reduction in bleeding outcomes in patients having PCI.


Similarly, STOPDAPT-2 suggested that in patients receiving PCI for stable ischemic heart disease and ACS, clopidogrel monotherapy might be continued after 1 month.


Switching to prasugrel 5 mg daily after 1 month was preferable to continuing with prasugrel 10 mg daily in HOST-REDUCE-POLYTECH-ACS. As a result, more complete revascularization, even of lesions that appear angiographically severe but do not cause ischemia per se, may be beneficial.

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