The purpose of this study is to determine whether Fractional flow reserve (FFR, (coronary pressure wire-based index for assessing the ischemic potential of a coronary lesion)-guided percutaneous coronary intervention (PCI) in patients with multivessel coronary artery disease (CAD) will result in similar outcomes to coronary artery bypass graft surgery (CABG).
The FAME 3 trial is a multicenter, international, randomized, controlled noninferiority trial. All patients with multivessel CAD (not involving the left main) will be screened by the site's Heart Team (including but not limited to an interventional cardiologist, cardiac surgeon and research coordinator). If all agree that the patient can be treated either with FFR-guided PCI or CABG, and all inclusion criteria are met and no exclusion criteria are met, then the patient will be randomized. Baseline clinical, functional, laboratory and electrocardiographic data will be obtained. Patients will receive treatment within 4 weeks of randomization. Patients randomized to CABG will receive state of the art therapy at the discretion of the local surgeon with a strong emphasis on arterial revascularization. Patients undergoing PCI will have FFR measured with a St. Jude Medical coronary pressure wire across all lesions. If the FFR is ≤0.80, then PCI will be performed with the Medtronic Resolute Integrity drug-eluting stent (DES) as per usual routine. If the FFR is \>0.80 then PCI will be deferred. All patients will receive medical therapy as per published guidelines. Patients will follow-up at 1 and 6 months, and 1 and 3 years with an evaluation of clinical status, functional status, medications and events. Follow-up may be extended to 5 years, if funding allows. Core lab analyses will include formal quantitative coronary angiography (QCA) of the baseline angiograms with calculation of the Synergy between Percutaneous Coronary Intervention with Taxus and Cardiac Surgery (SYNTAX) score and Functional SYNTAX Score.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
1,500
Coronary Artery Bypass Graft Surgery (CABG)
Durable polymer zotarolimus-eluting stent
Durable polymer zotarolimus-eluting stent
Palo Alto VA
Palo Alto, California, United States
Stanford University
Stanford, California, United States
Atlanta VA Medical Center
Decatur, Georgia, United States
Jesse Brown VA Medical Center
Chicago, Illinois, United States
University of Kansas Medical Center
Lawrence, Kansas, United States
MACCE
Death, MI, stroke and any repeat revascularization (MACCE) will be evaluated at 1 year, where subjects contribute data from time of randomization until the occurrence of MACCE or one year follow-up, whichever occurs first. Subjects who die or are lost to follow up before 1 year will be censored at their last recorded activity.
Time frame: 1 year
Key Secondary Outcome: Composite of Death From Any Cause, Myocardial Infarction, or Stroke
Death, MI, or stroke at 3-year follow-up
Time frame: 3 years
Number of Participants Experiencing Death, MI, or Stroke
Subjects who died or are lost to follow up before this time were censored at their last recorded activity.
Time frame: 1 year
Death
Death evaluated excluding patients lost to follow-up from each arm
Time frame: 1 year
Number of Participants Experiencing Myocardial Infarction
MI evaluated excluding patients lost to follow-up from each arm
Time frame: 1 year
Number of Participants Experiencing Stroke
Stroke evaluated excluding patients lost to follow-up from each arm.
Time frame: 1 year
Number of Participants Requiring Repeat Revascularization
Any repeat revascularization evaluated excluding patients lost to follow-up from each arm
Time frame: 1 year
Number of Participants Experiencing BARC Type 3-5 Bleeding
Bleeding Academic Research Consortium (BARC) type 3-5 indicates severe bleeding.
Time frame: 1 year
Number of Participants Experiencing Acute Kidney Injury
Time frame: 1 year
Number of Participants Experiencing Atrial Fibrillation or Clinically Significant Arrhythmia
Time frame: 1 year
Number of Participants Experiencing Definite Stent Thrombosis
Time frame: 1 year
Number of Participants Experiencing Definite Symptomatic Graft Occlusion
Time frame: 1 year
Number of Participants Requiring Rehospitalization Within 30 Days
Time frame: 30 days
MACCE
Death, MI, stroke and any repeat revascularization (MACCE) rate at 2 years, 3 years and 5 years
Time frame: 2 years, 3 years, 5 years
Death, MI, or Stroke at 5 Years
Death, MI, or stroke at 5 years
Time frame: 5 years
Individual Components of Primary Outcome
Individual components of primary outcome: number of participants experiencing death, myocardial infarction, and stroke
Time frame: At year 3
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Lexinton VA
Lexington, Kentucky, United States
University of Kentucky Medical Center
Lexington, Kentucky, United States
Baystate Medical Center
Springfield, Massachusetts, United States
HealthEast St. Joseph's Hospital
Saint Paul, Minnesota, United States
Penn Presbyterian Medical Center
Philadelphia, Pennsylvania, United States
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