Antithrombotic Strategy for AF Patients With High Risk CAD

Not Applicable

Not yet recruiting

• Conditions: Atrial Fibrillation; Coronary Artery Disease
• Interventions: Drug: Anticoagulation Monotherapy; Drug: Combination therapy

• Registration Number: NCT06866665
• Lead Sponsor: Yonsei University

Brief Summary

Anticoagulation therapy is recommended for patients with atrial fibrillation (AF) in order to prevent ischemic stroke and systemic embolism. Meanwhile, lifelong antiplatelet therapy is highly recommended to prevent stent thrombosis and further ischemic adverse events after percutaneous coronary intervention (PCI) with drug-eluting stent (DES) implantation. In this context, in patients with AF undergoing DES implantation, anticoagulation and antiplatelet therapies perform their own unique roles. However, the current guidelines recommend to discontinue this antiplatelet agent beyond 1 year due to an excessive bleeding risk derived from DAT.

The Atrial Fibrillation and Ischemic Events with Rivaroxaban in Patients with Stable Coronary Artery Disease (AFIRE) emphasized that bleeding risk derived from rivaroxaban-based DAT may outweigh ischemic risk derived from antiplatelet discontinuation in patients with AF and stable coronary artery disease. Furthermore, the recent Edoxaban versus Edoxaban with Antiplatelet Agent in Patients with Atrial Fibrillation and Chronic Stable Coronary Artery Disease (EPIC-CAD) trial also demonstrated that edoxaban monotherapy led to a lower net adverse event compared to than edoxaban-based DAT.

Although these studies strongly supported the benefit of antiplatelet discontinuation in AF patients with stable coronary artery disease, many physicians still hesitate to discontinue antiplatelet agents even 1 year after DES implantation because of concerns regarding stent thrombosis or subsequent myocardial infarction (MI). This concern is exacerbated in patients with an excessive ischemic risk, such as those who received complex PCI or those with polyvascular disease. To address this disparity between clinical practice and recommendations based on the guidelines, the Adequate Antiplatelet and Anticoagulation Therapy in Atrial Fibrillation Patients with Focus on Ischemic Risk Management (ADAPT AFFIRM) trial is designed to elucidate the efficacy and safety of apixaban monotherapy versus apixaban plus clopidogrel combination therapy as a chronic maintenance strategy in AF patients with stable coronary artery disease and excessive ischemic risk.

Detailed Description

Investigators will recruit 1400 patients with atrial fibrillation (AF) and coronary artery disease (CAD) with high ischemic risk. High ischemic risk is defined as acute myocardial infarction, complex percutaneous coronary intervention (PCI), untreated significant coronary stenosis, or polyvascular disease. Paticipants will be randomly assigned to either anticoagulation monotherapy group or combination therapy group. Participants assigned to the anticoagulation monotherapy group wil receive apixaban 5 mg twice daily (or reduced dose as judged by investigators) and those assigned to the combination therapy group will receive additional clopidogrel 75 mg daily on top of apixaban. Net adverse clinical events comprising all-cause death, myocardial infarction, stroke, systemic embolism, or ISTH major or clinically relevant non-major bleeding events will be evaluated at 12 months after randomization. Included participant will be followed up until the last participant will be followed up for at lease 12 months.

Study Timeline

• Study First Submitted: 2025-02-23
• Status Verified: 2025-03
• Study Start: 2025-03
• Study First Submitted QC: 2025-03-06
• Study First Posted: 2025-03-10
• Last Update Submitted: 2025-03-11
• Last Update Posted: 2025-03-14
• Primary Completion: 2030-12
• Study Completion: 2030-12

Recruitment & Eligibility

• Status: NOT_YET_RECRUITING
• Sex: All
• Target Recruitment: 1400

Inclusion Criteria

1. ≥ 19 years old
2. Presence of AF with CHA2DS2-VASc score ≥ 2
3. Patients with stable CAD - a history of percutaneous coronary intervention (PCI) or coronary artery bypass graft surgery (CABG) before 6 months (chronic coronary syndrome) or 12 months (acute coronary syndrome); anatomically confirmed CAD on coronary angiography or computed tomography scan
4. Presence of an excessive ischemic risk i. A history of myocardial infarction (MI) ii. Complex PCI iii. Untreated lesion with >50% stenosis at major epicardial vessel after coronary revascularization iv. Untreated multivessel CAD (>50% stenosis of >1 major epicardial vessel or left main stem) v. Peripheral artery disease vi. Cerebrovascular disease

Exclusion Criteria

1. >85 years old.
2. Patients who received PCI or CABG within 6 months.
3. Patients with a history of acute coronary syndrome within 12 months.
4. Patients who require anticoagulation with warfarin due to a mechanical prosthetic valve, or ≥ moderate mitral stenosis.
5. Patients with a comorbidity requiring anticoagulation other than AF.
6. Patients who is not able to receive apixaban or clopidogrel due to previous adverse reaction.
7. Patients who have coagulopathy or have a history of recurrent bleeding.
8. Intracranial or gastrointestinal bleeding within 3 months.
9. Gastrointestinal tumor requiring treatment.
10. Patients who are pregnant or those who report potential pregnancy.
11. Life expectancy < 1 year due to malignancy.
12. Refuse or enable to understand the written informed consent.
13. Patiens who are not able to discontinue a drug related to CYP3A4 inhibition.

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
Anticoagulation Monotherapy	Anticoagulation Monotherapy	Participants receiving anticoagulation monotherapy
Combination therapy	Combination therapy	Particiapnts receiving anticoagulation therapy with additional clopidogrel

Primary Outcome Measures

Name	Time	Method
Net adverse clinical event (NACE)	12 months after the last enrollment	NACE is defined as a composite of all-cause death, MI, stroke, systemic embolism, and major or clinically relevant non-major (CRNM) bleeding as defined by International Society on Thrombosis and Hemostasis (ISTH) criteria.

Secondary Outcome Measures

Name	Time	Method
Composite bleeding event	12 months after the last enrollment	Composite bleeding event: a composite of ISTH major or CRNM bleeding
Major adverse cardiac event	12 months after the last enrollment	Major adverse cardiac event (MACE): a composite of cardiovascular death, MI, or any coronary revascularization
Key ischemic event	12 months after the last enrollment	Key ischemic event: a composite of cardiovascular death, MI, ischemic stroke, or systemic embolism
Each components of NACE	12 months after the last enrollment	MI
Cardiovascular death	12 months after the last enrollment
Non-cardiovascular death	12 months after the last enrollment
Ischemic stroke	12 months after the last enrollment
Hemorrhagic stroke	12 months after the last enrollment
Any coronary revascularization	12 months after the last enrollment	PCI (Percutaneous Coronary Intervention), CABG(Coronary Artery Bypass Graft)
Acute limb ischemia	12 months after the last enrollment
Any limb revascularization or amputation	12 months after the last enrollment	1. Endovascular revascularization; 2. Surgical revascularization; 3. Amputation
Any intracranial revascularization	12 months after the last enrollment	1. Endovascular revascularization; 2. Surgical revascularization
A composite of cardiovascular death, MI, acute limb ischemic, or any limb revascularization or amputation	12 months after the last enrollment
A composite of cardiovascular death, MI, acute limb ischemia, or ischemic stroke	12 months after the last enrollment