Comparison of clinical outcomes following percutaneous coronary intervention versus optimal medical therapy based on gray-zone fractional flow reserve in stable angina patients with intermediate coronary artery stenosis (COMFORTABLE prospective study): Study protocol for a multicenter randomized controlled trial
Even in the current drug-eluting stent era, revascularization for coronary stenosis with fractional flow reserve (FFR) between 0.75 and 0.80, the so-called “gray zone,” is a matter of debate. Previous studies have reported conflicting results regarding outcomes of revascularization versus deferral for coronary stenosis when FFR values are in the gray zone, but these studies have had differing designs and populations. We therefore will investigate whether medical therapy plus percutaneous coronary intervention (PCI) is superior to medical therapy alone in reducing major cardiovascular events in patients presenting with coronary stenosis with gray zone FFR values.
This is a prospective, multicenter, open-label, parallel group, randomized, controlled, superiority study. A total of 410 eligible participants will be recruited and randomized to either the medical therapy plus PCI group or the medical therapy alone group. The primary endpoint is 1-year major adverse cardiac events (MACEs), defined as a combined endpoint of all-cause death, nonfatal myocardial infarction (MI), or unplanned target vessel revascularization (TVR). Secondary endpoints include MACE at 2 and 5 years. Moreover, each individual component of the primary endpoint, cardiovascular death, target vessel-related and non-target vessel-related MI, all MI, clinically driven TVR or non-TVR, all revascularization, stent thrombosis, and angina symptom status will be evaluated at 1, 2, and 5 years.
This is the first prospective, multicenter, randomized, controlled study to investigate the superiority of medical therapy plus PCI over medical therapy by itself in reducing major cardiovascular events in patients presenting with coronary stenosis with “gray zone” FFR values. The results will help interventional cardiologists in making revascularization decisions regarding coronary stenosis with gray zone FFR values.
University Hospital Medical Information Network Clinical Trials Registry, UMIN000031526. Registered on 1 March 2018.
KeywordsCoronary physiology Fractional flow reserve Medical therapy Percutaneous coronary intervention
Coronary artery bypass grafting
Consolidated Standards of Reporting Trials
Fractional flow reserve
Left main coronary artery
Major adverse cardiac event
Percutaneous coronary intervention
Standard Protocol Items: Recommendations for Interventional Trials
Target vessel revascularization
Coronary physiological assessment can more effectively guide management decisions on intermediate coronary stenotic lesions than coronary anatomical assessment. This allows determination of whether the patient would benefit from revascularization or medical therapy.
Fractional flow reserve (FFR) is an established invasive index for determination of the functional severity of a coronary stenosis. FFR values < 0.75 were shown to be associated with inducible myocardial ischemia with > 99% positive predictive value . The DEFER study (Deferral versus performance of percutaneous coronary intervention (PCI) of functionally non-significant coronary stenosis) has since demonstrated that PCI can be safely deferred in coronary stenosis with FFR ≥ 0.75 . In addition, at 15-year follow-up, it was reported that the rate of myocardial infarction (MI) was significantly lower in the deferred group than in the revascularization group (2.2% versus 10%) . On the contrary, PCI for coronary stenosis with FFR ≤ 0.80, compared with medical therapy by itself, is associated with improved clinical outcomes [4, 5, 6, 7, 8]. Nonetheless, revascularization for coronary stenosis with FFR between 0.75 and 0.80, the so-called gray zone, is still an unresolved issue. Owing to differing study designs and populations, previous studies have reported conflicting results regarding outcomes of revascularization versus deferral for coronary stenosis with gray zone FFR values [9, 10, 11, 12, 13, 14, 15, 16, 17].
We therefore will conduct a prospective, multicenter, randomized, controlled trial to investigate whether medical therapy plus PCI is superior to medical therapy alone in reducing major cardiovascular events in patients presenting with coronary stenosis with gray zone FFR values.
The Comparison of clinical outcomes following percutaneous coronary intervention versus optimal medical therapy based on gray zone fractional flow reserve in stable angina patients with intermediate coronary artery stenosis (COMFORTABLE) study is designed as a prospective, multicenter, open-label, parallel group, randomized, controlled, superiority study. This study is being conducted across 11 hospitals in Wakayama Prefecture and Tokyo, Japan. A total of 410 eligible participants will be recruited and randomized into either the performed PCI group or the deferred PCI group, with an allocation ratio of 1:1. Recruitment will begin soon.
The aim of this study is to determine whether medical therapy plus PCI is superior to medical therapy by itself in reducing major cardiovascular events in patients presenting coronary stenosis with “gray zone” FFR values.
Participants will be eligible for registration in this study if they meet all of the inclusion criteria and none of the exclusion criteria listed in the subsections below.
Intermediate coronary stenosis presenting with an FFR between 0.75 and 0.80
Aged ≥ 20 years
Able to provide written informed consent prior to any study-specific procedures
Culprit vessel in acute coronary syndrome
Untreated significant lesions (percentage of diameter stenosis > 70% and/or FFR < 0.75) in coronary arteries other than the target vessel
Previous coronary artery bypass grafting (CABG)
Allergy to antiplatelet therapy, anticoagulants, or contrast medium
Intracranial and/or gastrointestinal bleeding
Planned surgical procedure within 12 months
Life expectancy < 1 year
Severe valvular heart disease
Participation in clinical trials of other devices or drugs
Left main coronary artery (LMCA) disease (percentage of diameter stenosis > 50%) or planned PCI for LMCA disease
Chronic total occlusions
Heavily calcified or tortuous vessels, meaning inability to cross the lesion with a pressure wire is expected
Diffuse diseases, heavily calcified lesions, small vessels, and/or aneurysmal lesions, meaning PCI is thought to be unsuitable by operators
Eligible participants will be allocated to one of the two groups (medical therapy plus PCI group or medical therapy alone group) by the online randomization system. Balanced randomization based on critical variables (diabetes, age, sex, and institution) will be performed automatically by the randomization algorithm. Knowledge of the treatment allocation is open to the investigators and participants.
Sample size calculation
On the basis of event rates of previous studies that evaluated deferred versus performed revascularization in patients presenting coronary stenosis with gray zone FFR values, we predicted that the event rates at 1 year would be 6.4% in the revascularization group and 16% in the deferred group . Under the above event rates and the hypothesis that the crossover rate from the medical therapy alone arm to the PCI arm is 5%, we calculated that a sample size of 368 patients (184 per arm) would provide the trial with 80% power to detect the superiority of medical therapy plus PCI over medical therapy by itself, at a two-sided alpha level of 5%. Assuming a dropout rate of 10% (patients lost to follow-up or patients unsuitable for analysis), the target sample size was set at 410 patients (205 per arm).
The primary endpoint is 1-year major adverse cardiac events (MACE), defined as a combined endpoint of all-cause death, nonfatal MI, or unplanned target vessel revascularization (TVR). Secondary endpoints will include MACE at 2 and 5 years. Each individual component of the primary endpoint, cardiovascular death, target vessel-related and non-target vessel-related MI, all MI, clinically driven TVR or non-TVR, all revascularization, stent thrombosis, and angina symptom status will also be evaluated at 1-, 2-, and 5-year follow-up. All-cause death is defined as death of any cause, cardiovascular as well as noncardiovascular. MI is defined as a clinical episode of typical chest pain with development of new Q waves in at least two contiguous leads on an electrocardiogram or elevation of the creatine kinase myocardial band fraction (spontaneous, above the upper reference limit; periprocedural, more than three times the upper reference limit). Unplanned revascularization is defined as any unexpected coronary revascularization (PCI or CABG) during the follow-up period after the index procedure. TVR is defined as any repeat revascularization of any segment of the target vessel by either PCI (additional stent or angioplasty) or CABG. TVR will be considered to be ischemia-driven if revascularization is performed on a patient who has ischemic signs confirmed by noninvasive tests or FFR reassessment (with an inducible ischemia cutoff set at < 0.75), despite the presence or absence of ischemic symptoms. TVR will be considered to be clinically driven if revascularization is performed on a patient who has ischemic signs confirmed by noninvasive tests or FFR reassessment and clinical symptoms, such as chest pain that increases in frequency, intensity, or duration. Stent thrombosis is defined according to Academic Research Consortium definition . Anginal status is assessed by Canadian Cardiovascular Society functional classification of angina. Clinical events are adjudicated by an independent and blinded clinical event committee.
Coronary angiography will be performed in the standard manner via a transradial or transfemoral approach in each center. Intracoronary (IC) isosorbide dinitrate or nitroglycerin is administered in all cases preceding coronary angiography. A coronary angiogram is obtained from a standard series of six to eight projections for the left coronary artery and two or three projections for the right coronary artery. All images are stored on a CD-ROM for offline analysis. Diameter stenosis, minimum lumen diameter, lesion length, and reference lumen diameter will be measured by using dedicated software for quantitative coronary angiography (CASS-5; Pie Medical, Maastricht, The Netherlands). Quantitative coronary angiographic analysis is conducted at the Core Laboratory of Wakayama Medical University, Wakayama, Japan.
IC pressure will be measured using a pressure wire system (PressureWire, Abbot Vascular, Santa Clara, CA, USA; Smartwire, Philips Volcano, San Diego, CA, USA; Comet, Boston Scientific, Marlborough, MA, USA; or OptoWire, Zeon Medical, Tokyo, Japan). FFR measurement will be done as reported previously . In brief, following pressure zero-calibration and equalization, the pressure wire will be placed in the distal part of the target coronary artery. IC nitroglycerin is administered prior to FFR measurement. FFR is calculated as the mean distal coronary pressure, measured by the pressure wire, divided by the mean aortic pressure, simultaneously measured by the guiding catheter during maximal hyperemia. Maximal hyperemia will be induced by intravenous continuous infusion of adenosine 5′-triphosphate (ATP), given at 180 μg/kg/min via the forearm or femoral vein. If maximal hyperemia is suspicious, additional IC papaverine (12 mg for left coronary artery or 8 mg for right coronary artery), IC nicorandil (2 mg for both coronary arteries), or IC ATP (50 μg for left coronary artery or 25 μg for right coronary artery) administration will be recommended. In case of contraindication to ATP, IC papaverine or IC nicorandil should be administered alternatively. After distal pressure measurement is done, the pressure sensor is pulled back to the ostium of the guiding catheter during maximal hyperemia, and both pressures are checked to exclude any transducer drift. Where drift is evident (Pd/Pa < 0.98 or > 1.02 measured at the level of the catheter tip), measurements should be repeated. Because caffeine attenuates ATP-induced hyperemia by blocking activation of adenosine A2a receptor in vascular smooth muscles, patients should refrain from consuming products containing caffeine 24 h (at least 12 h) before FFR measurement [19, 20].
In the medical therapy plus PCI group, PCI will be performed in the standard manner according to clinical guidelines at the time of the procedure by using currently available second-generation or third-generation drug-eluting stents (DES). The choice of approach site (transradial or transfemoral) is at the operator’s discretion. Also, the type of DES and the use of intravascular imaging are at the discretion of the operator. Patients who underwent PCI will be treated with aspirin (100 mg/day) and thienopyridines (clopidogrel 75 mg/day or prasugrel 3.75 mg/day) for at least 6 months, followed by aspirin indefinitely.
Guideline-directed optimal medical therapy will be applied to all participants, regardless of the treatment arm.
Data collection and follow-up
The data will be collected using a web-based dedicated case report form. All data management and analysis will be performed centrally at the Department of Cardiovascular Medicine at the coordinating center (Wakayama Medical University, Wakayama, Japan). Members of the coordinating Center monitor and verify the data in the participating hospitals. Clinical follow-up will be performed during hospitalization; at discharge; and at 1 year, 2 years, and 5 years after allocation. The patient’s clinical status, medications, and adverse events will be evaluated and recorded during office visits or by qualified personnel via telephone contacts if office visits are impractical or impossible.
Safety is observed throughout the study. During the study period, all participants will be monitored and evaluated for clinical events and any other adverse events by the data and safety monitoring committee.
Continuous variables will be summarized as mean ± SD or median (IQR) for skewed data, and comparisons will be made using an unpaired Student’s t test or Mann-Whitney’ U test as appropriate. Categorical variables will be summarized as number (%), and comparisons will be made using the chi-square test or Fisher’s exact test as appropriate. Kaplan-Meier survival analysis curves will be used to assess clinical event timelines and will be compared with the log-rank test. Also, in time-to-event analyses, the treatment groups will be compared using a Cox proportional hazards model, and the results will be expressed as an HR with 95% CI. Values of p < 0.05 will be considered statistically significant. All statistical analyses will be conducted using JMP Pro version 14 software (SAS Institute, Cary, NC, USA).
Even in the current DES era, revascularization for coronary stenosis with FFR between 0.75 and 0.80 is a matter of debate. Some studies, including our retrospective studies [12, 17], have reported that PCI compared with medical therapy alone is associated with better clinical outcomes in patients with gray zone FFR values [9, 11, 14, 15]. Conversely, other studies have shown that deferred revascularization could be the preferred initial treatment strategy for coronary stenosis with gray zone FFR values [10, 13, 16]. Thus, revascularization versus deferral decision-making for coronary stenosis presenting with gray zone FFR is controversial. However, currently available evidence is limited to registries, retrospective analyses, and single-center experiences. For FFR values between 0.75 and 0.80, the clinical decision for PCI or medical therapy has been left entirely to the operator’s discretion.
The COMFORTABLE prospective study will be the first prospective, multicenter, randomized, controlled study to prove the superiority of medical therapy plus PCI over medical therapy alone in reducing major cardiovascular events in patients presenting with coronary stenosis with gray zone FFR values. The results of the COMFORTABLE prospective study will help interventional cardiologists guide revascularization decisions for coronary stenosis with gray zone FFR values.
This study has several limitations, the most important being its open-label nature. We cannot entirely exclude the possibility that the treatment strategy will be modified, because the arm of treatment to which the patient has been allocated will be known. Second, an FFR value is limited by its reliance on the achievement of maximal hyperemia. Failure to achieve peak hyperemia, by not achieving maximal reduction in microvascular resistance, may result in overestimation of FFR and lead to wrong decision-making, especially in coronary stenosis with an FFR value in and around the “gray zone” . For these reasons, in this study, we will use intravenous ATP administration to induce steady-state maximal hyperemia, and additional IC papaverine, nicorandil, or ATP should be administered if maximal hyperemia is suspicious.
The Wakayama Medical University Institutional Review Board approved the final version of the protocol prior to the start of the study (approval number 2234). The study is registered with the University Hospital Medical Information Network Clinical Trials Registry (UMIN000031526). The trial will open for recruitment soon.
We acknowledge proofreading by Benjamin Phillis at the Clinical Study Support Center, Wakayama Medical University.
This study is supported by the Japan Research Foundation for Healthy Aging. This funding body is only providing financial support and has no role in the design of the study protocol, the writing of the manuscript, the analysis and interpretation of the data, or the decision to submit the report for publication.
Availability of data and materials
HK, TK, and YS designed the study protocol and drafted the manuscript. TA further aided in assessment and revision of the protocol and revised the manuscript. The COMFORTABLE study group members, including KS, YI, TT, YH, KK, HS, KK, MG, TH, MO, KM, and JY, contributed to the initial conception of the study design. YS provided the statistical analysis. All authors carefully read and approved the final version of the manuscript.
Ethics approval and consent to participate
The study is conducted in accordance with the Declaration of Helsinki. Wakayama Medical University Institutional Review Board approved the final version of the protocol (version 1.1) prior to the start of the study (approval number: 2234). This study was registered on the University Hospital Medical Information Network Clinical Trials Registry (UMIN000031526). Written informed consent will be obtained from all participants in the study.
Consent for publication
The authors declare that they have no competing interests.
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