Key result
Genotype-guided antiplatelet therapy provides more QALYs at ~$4,200 each versus clopidogrel and dominates prasugrel.
Why the study?
Prasugrel is recommended over clopidogrel in poor/intermediate CYP2C19 metabolizers with ACS and planned PCI, but the cost-utility of genotype-guided antiplatelet therapy was not evaluated from the US healthcare provider perspective.
Does genotype-guided antiplatelet therapy improve cost-effectiveness compared to prasugrel or clopidogrel without genotyping in patients with moderate-to-high risk acute coronary syndrome and planned percutaneous coronary intervention?
Does genotype-guided antiplatelet therapy improve cost-effectiveness compared to prasugrel or clopidogrel without genotyping in patients with moderate-to-high risk acute coronary syndrome and planned percutaneous coronary intervention?
Effect estimate: ICUR USD 4,200/QALY
Absolute Event Rate: 10.05% vs 10.03%
Genotype-guided antiplatelet therapy is a cost-effective strategy compared to universal clopidogrel or prasugrel in patients with ACS undergoing planned PCI.
May support cost-effectiveness of genotype-guided antiplatelet therapy in ACS-PCI; leaves open prospective validation before practice change.
BACKGROUND: Prasugrel is recommended over clopidogrel in poor/intermediate CYP2C19 metabolizers with acute coronary syndrome (ACS) and planned percutaneous coronary intervention (PCI), reducing the risk of ischemic events. CYP2C19 genetic testing can guide antiplatelet therapy in ACS patients. OBJECTIVE: The purpose of this study was to evaluate the cost-utility of genotype-guided treatment, compared with prasugrel or generic clopidogrel treatment without genotyping, from the US healthcare provider's perspective. METHODS: A decision model was developed to project lifetime economic and humanistic burden associated with clinical outcomes (myocardial infarction [MI], stroke and major bleeding) for the three strategies in patients with ACS. Probabilities, costs and age-adjusted quality of life were identified through systematic literature review. Incremental cost-utility ratios (ICURs) were calculated for the treatment strategies, with quality-adjusted life years (QALYs) as the primary effectiveness outcome. Relative risk of developing myocardial infarction and stroke between patients with and without variant CYP2C19 when receiving clopidogrel were estimated to be 1.34 and 3.66, respectively. One-way and probabilistic sensitivity analyses were performed. RESULTS: Clopidogrel cost USD19,147 and provided 10.03 QALYs versus prasugrel (USD21,425, 10.04 QALYs) and genotype-guided therapy (USD19,231, 10.05 QALYs). The ICUR of genotype-guided therapy compared with clopidogrel was USD4,200. Genotype-guided therapy provided more QALYs at lower costs compared with prasugrel. Results were sensitive to the cost of clopidogrel and relative risk of myocardial infarction and stroke between CYP2C19 variant vs. non-variant. Net monetary benefit curves showed that genotype-guided therapy had at least 70% likelihood of being the most cost-effective alternative at a willingness-to-pay of USD100,000/QALY. In comparison with clopidogrel, prasugrel therapy was more cost-effective with <21% certainty at willingness-to-pay of >USD170,000/QALY. CONCLUSIONS: Our modeling analyses suggest that genotype-guided therapy is a cost-effective strategy in patients with acute coronary syndrome undergoing planned percutaneous coronary intervention.
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Patel et al. (2014) studied Moderate-to-high risk acute coronary syndrome with planned percutaneous coronary intervention. Genotype-guided antiplatelet therapy vs. Clopidogrel or prasugrel without genotyping was evaluated on Incremental cost-utility ratio (ICUR) per quality-adjusted life year (QALY) gained (ICUR USD 4,200/QALY). Genotype-guided antiplatelet therapy provided more QALYs at an incremental cost of USD 4,200 per QALY gained compared with clopidogrel, and dominated prasugrel therapy.
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