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EuroPCR 2024 – One-month DAPT followed by 5-month Ticagrelor monotherapy in acute coronary syndromes with DCB - results from REC-CAGEFREE II

2024-05-15
(Press-News.org) Paris, France, 14-17 May 2024. The Course Directors have selected 3 major Late Breaking Trials (LBTs) that will be presented for the first time during the 2024 edition of EuroPCR. These trials were selected on account of their design, outcomes and potential to influence daily clinical practice. Among them is the REC-CAGEFREE II trial. 

Background and methods  The REC-CAGEFREE II trial is an open-label, investigator-initiated, non-inferiority, multicentre randomised trial comparing stepwise de-escalation of dual antiplatelet therapy (DAPT) with standard DAPT in patients with acute coronary syndrome (ACS) treated with paclitaxel-coated balloons (PCB). Eligible patients were randomly assigned to stepwise DAPT de-escalation − consisting of aspirin plus ticagrelor for 1 month, followed by 5 months of ticagrelor monotherapy, and then 6 months of aspirin monotherapy − compared to standard DAPT (aspirin plus ticagrelor for 12 months). The primary efficacy endpoint was net adverse clinical events (a composite of all-cause death, stroke, myocardial infarction [MI], revascularisation, and Bleeding Academic Research Consortium [BARC] type 3 or 5 bleeding) at 1 year.

Results  A total of 1,948 patients were enrolled and randomised to stepwise DAPT de-escalation (n=975) or standard DAPT (n=973). The study shows that stepwise DAPT de-escalation was non-inferior to standard 12-month DAPT for the primary endpoint in patients with ACS treated exclusively with PCB (87 [9.0%] vs 84 [8.7%]; difference: 0.3%, upper boundary of the one-sided 95% confidence interval [CI]: 2.4%; p non-inferiority=0.01). The rates of BARC type 3 or 5 bleeding were 0.4% and 1.7% (difference: −1.24%, 95 % CI: −2.14 to −0.33), and the rates of the composite of all-cause death, stroke, MI, and revascularisation were 8.8% and 7.6% (difference: 1.03%, 95 CI%: −1.40 to 3.47) in the stepwise de-escalation and standard groups, respectively. 

Key learnings  The major strength of this study is that it provides the first randomised evidence regarding antiplatelet therapy strategy in drug-coated balloon (DCB) percutaneous coronary intervention (PCI). One of the potential advantages of using DCB is the need for shorter duration DAPT, given the lack of stent struts requiring endothelialisation. However, patients with ACS have higher ischaemic risk, and current guidelines still recommend DAPT for 12 months in patients without high bleeding risk.

The present study supports the value of de-escalation therapy with ticagrelor in ACS patients treated with DCB. However, some important considerations remain. First, evidence for the use of DCB in the context of de novo lesions (particularly in patients with ACS) is quite limited, with no randomised data to demonstrate adequate results in this context. Second, only around 40% of subjects underwent PCI for ST-elevation myocardial infarction (STEMI) or non-STEMI (NSTEMI), while the rest had unstable angina. Application of the results to higher-risk patients with STEMI or NSTEMI is therefore debatable.  Third, only 9% of all eligible patients were enrolled, indicating a very selected population. The main reason for exclusion was use of a drug-eluting stent (DES) in another vessel, raising concerns about the feasibility of a PCB-only strategy in patients with ACS, who often have multivessel disease, and the external validity of the data.  Fourth, with regard to the procedure, only PCB were used, and 60% of the lesions treated were in small vessels (mean PCB diameter: 2.7 mm). In most patients, only one lesion was treated, again suggesting a very selected, low-risk population. Finally, several types of PCB were used, mostly without robust clinical evidence for their use in de novo lesions.  There is no class effect for these devices, whose efficacy is influenced by multiple factors such as dose, formulation and release kinetics.  

Conclusions and PCR recommendations  REC-CAGEFREE II is a pioneering study that provides the first randomised data concerning the use of antiplatelet therapy in the context of DCB. The results, however, are probably only applicable to low-risk populations (mainly those with unstable angina with single small vessel disease). Using DCB in the context of ACS poses theoretical advantages, including recovery of endothelial function and the lack of delayed endothelialisation and late acquired malapposition. These potential benefits require testing in adequately designed trials comparing the use of DCB in de novo lesions in ACS patients to DES (the current standard of care).

 

NOTES TO EDITORS

Key information 

Session: Hotline/Late-Breaking Trials: Major Late-Breaking Trials from EuroPCR 2024  Presentation: One-month DAPT followed by 5-month Ticagrelor monotherapy in acute coronary syndromes with DCB  Presenter: Ling Tao  Palais des Congrès Porte Maillot – Paris, France  Wednesday 15 May 2024 – presentation time 08:30 CEST (session time 08:30-10:00) – Theatre Bleu  About EuroPCR 2024   The World-Leading Course in interventional cardiovascular medicine and the official annual meeting of the European Association of Percutaneous Cardiovascular Interventions (EAPCI) will take place from 14 to 17 May 2024, onsite at the Palais des Congrès, Paris, France. A digital package is also available for those unable to join in person.  

The detailed Course Programme is available on: https://www.pcronline.com/Courses/EuroPCR/Programme   

About PCR   The mission of PCR is to serve the needs of each individual patient by helping the global cardiovascular community to share knowledge, experience and practice. PCR offers a large range of many other educational meetings and resources for the continuing education of the interventional cardiovascular community. These include major annual courses across the globe, e-learning with high-profile PCR Webinars, courses specifically dedicated to valvular heart disease, tailor-made PCR Seminars on specific topics, online resources and medical publications such as EuroIntervention, the official journal of the EAPCI.  

Gateways to all PCR activities are available on www.pcronline.com

For further information, please contact Sally Collingridge: scollingridge@europa-group.com  

About the EAPCI    The European Association of Percutaneous Cardiovascular Interventions (EAPCI) is a branch of the European Society of Cardiology. Its mission is to reduce the burden of cardiovascular disease through percutaneous cardiovascular interventions. This dynamic association represents a large community of over 8K EAPCI associates and over 1K full EAPCI members by helping them remain up to date in the constantly evolving field of PCI by publishing research and providing educational, training and certification programmes. The EAPCI also advocates for the best possible access to life saving treatments for patients through data-based advocacy at a European level.   

HELP FOR JOURNALISTS TO COVER EUROPCR 2024  

Register and attend EuroPCR 2024 as a journalist  

Open to accredited journalists, free of charge. Journalists must hold a valid press card and/or provide a letter of assignment from a recognised publication. To register as press, go to  
https://www.pcronline.com/Courses/EuroPCR/Press  

EuroPCR press releases can be found at  
https://www.pcronline.com/News/PCR-Press-Releases

For any press-related enquiries, please contact  
EuroPCR Press Coordinator, Isabelle Uzielli: iuzielli@europcr.com  

 

END


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[Press-News.org] EuroPCR 2024 – One-month DAPT followed by 5-month Ticagrelor monotherapy in acute coronary syndromes with DCB - results from REC-CAGEFREE II