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Published on: August 28, 2018
Coronary Artery Calcium to Improve the Efficiency of Randomized Controlled Trials in Primary Cardiovascular
Miguel Cainzos-Achirica1, Marcio Sommer Bittencourt2, Albert D Osei3
1Division of Cardiovascular Prevention and Wellness, Department of Cardiology, Houston Methodist DeBakey Heart & Vascular Center, Houston, Texas, USA; Center for Outcomes Research, Houston Methodist, Houston, Texas, USA; Johns Hopkins Ciccarone Center for the Prevention of Cardiovascular Disease, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.
Insights
Coronary artery calcium (CAC) scoring effectively identifies high-risk individuals for atherosclerotic cardiovascular disease (ASCVD) primary prevention trials. Using CAC >400 significantly reduces sample size and costs for randomized controlled trials (RCTs).
Area of Science:
- Cardiology
- Preventive Medicine
- Clinical Trial Design
Background:
- Randomized controlled trials (RCTs) for primary prevention of atherosclerotic cardiovascular disease (ASCVD) face challenges in sample size and cost, particularly for novel add-on therapies.
- High-risk individuals treated with statins are a key population for these trials.
Purpose of the Study:
- To evaluate the utility of coronary artery calcium (CAC) scoring in enriching primary prevention RCT populations with individuals at high absolute risk of ASCVD events.
- To assess the impact of CAC scoring on sample size and cost-efficiency in clinical trials.
Main Methods:
- 3,075 statin-naive participants from the Multi-Ethnic Study of Atherosclerosis (MESA) with an estimated 10-year ASCVD risk of ≥7.5% were analyzed.
- Coronary artery calcium (CAC) scores (>100, >400) and other biomarkers were assessed as enrichment criteria.
- Projected 5-year cardiovascular disease (CVD) incidence, sample sizes, and costs for hypothetical RCTs were computed based on assumed relative risk reductions.
Main Results:
- A CAC score >400 identified subgroups with the highest 5-year incident events, reducing projected sample size by 33%–58% compared to risk estimation alone.
- Using CAC >400 resulted in the lowest projected RCT costs, with savings of at least $40 million.
- A CAC score >100 demonstrated the second-best performance in most scenarios.
Conclusions:
- High CAC scores serve as effective entry criteria for primary prevention RCTs.
- Implementing CAC scoring enhances the efficiency and feasibility of trials evaluating novel add-on therapies for ASCVD prevention.
Objectives:
This study sought to assess the value, in terms of sample size and cost, of using the coronary artery calcium (CAC) score to enrich the study population of primary prevention randomized controlled trials (RCTs) with participants at high absolute risk of atherosclerotic cardiovascular disease (ASCVD) events.
Background:
The feasibility of RCTs assessing the efficacy of novel add-on therapies for primary prevention among high-risk individuals treated with statins may be limited by sample size and cost.
Methods:
We evaluated 3,075 statin-naive participants from the MESA (Multi-Ethnic Study of Atherosclerosis) with estimated 10-year ASCVD risk of ≥7.5%. CAC of >100, CAC of >400, high sensitivity C-reactive protein levels of >2 and >3 mg/l, ankle-brachial index of <0.9, and triglyceride levels of >175 mg/dl were each evaluated as enrichment criteria on top of estimated ASCVD risk of ≥7.5%, ≥10%, ≥15% and ≥20%. For each criterion, using the observed 5-year incidence of CVD, we projected the incidence of CVD assuming a 28% relative risk reduction with high-intensity statin therapy and after addition of novel therapy with additive relative risk reductions of 15% and 25%. Sample size and cost of a hypothetical primary prevention 5-year RCT of a novel therapy on top of statins versus statins alone were then computed by using the projected incidences. Yearly costs per included participant of $6,000 to $9,000 and of $500/$600 per screened nonparticipant were assumed.
Results:
CAC of >400, present in 15% to 23% participants, consistently identified the subgroups with highest 5-year incident events and outperformed the other features yielding the smallest projected sample size, ranging 33% to 58% lower than using risk estimations alone for participant selection. CAC of >400 also yielded the lowest projected RCT costs, at least $40 million lower than using risk estimations alone. CAC of >100 showed the second-best performance in most scenarios.
Conclusions:
High CAC scores used as study entry criteria can improve the efficiency and feasibility of primary prevention RCTs evaluating the incremental efficacy of novel add-on therapies.
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