Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2017 Dec 1;2(12):1369-1374.
doi: 10.1001/jamacardio.2017.3655.

Updated Cost-effectiveness Assessments of PCSK9 Inhibitors From the Perspectives of the Health System and Private Payers: Insights Derived From the FOURIER Trial

Affiliations

Updated Cost-effectiveness Assessments of PCSK9 Inhibitors From the Perspectives of the Health System and Private Payers: Insights Derived From the FOURIER Trial

Alejandro Arrieta et al. JAMA Cardiol. .

Abstract

Importance: Preliminary cost-effectiveness analyses of proprotein convertase subtilisin/kexin type 9 inhibitor (PCSK9i) were based on benefits estimated from reductions in low-density lipoprotein cholesterol that occurred in PCSK9i trials with variable results. The recent Further Cardiovascular Outcomes Research with PCSK9 Inhibition in Subjects with Elevated Risk (FOURIER) trial provides better information about the effectiveness of the drug.

Objective: To use the trial results to determine the cost-effectiveness of a PCSK9i and statin treatment strategy compared with a statin alone strategy.

Design, setting, and participants: We derived observed rates of events, outcomes, cost of care, and health insurance from existing literature for a theoretical cohort of patients designed to resemble the FOURIER PCSK9i trial population and created a Markov model during the time horizon of a full lifetime.

Main outcomes and measures: We evaluated the incremental cost-effectiveness ratio from a health system perspective, and the return on investment from a private payer perspective. For both measures, we assumed an annual PCSK9i drug price of $14 300, with a lapse in US patent protection that would reduce the price by 43% in year 12. Costs were reported in 2016 US dollars.

Results: This study modeled 1000 hypothetical patients with attributes similar to those of the FOURIER trial cohort. At the current price, the incremental cost-effectiveness ratio of statin plus PCSK9i therapy was $337 729 per quality-adjusted life-year. Our probabilistic sensitivity analysis found that a statin plus PCSK9i strategy had a low probability (<1%) of being cost effective at the commonly accepted societal threshold of $100 000 per quality-adjusted life-year. Furthermore, PCSK9i produced a negative return on investment of 86% for private payers. In our threshold analysis, the price of PCSK9i would need to drop 62%, to $5459 per year, to reach $100 000 per quality-adjusted life year.

Conclusions and relevance: At current prices, the addition of PCSK9i to statin therapy is estimated to provide an additional quality-adjusted life year for $337 729 . Significant discounts are necessary to meet conventional cost-effectiveness standards.

PubMed Disclaimer

Conflict of interest statement

Conflict of Interest Disclosures: All authors have completed and submitted the ICMJE Form for Disclosure of Potential Conflicts of Interest. Dr Nasir is on the advisory board for Quest Diagnostic and is a consultant for Regeneron. Dr Arrieta has received research support or honoraria from the American Medical Association and the Pan American Health Organization. Dr Virani reported serving on the steering committee (with no financial remuneration) for the Patient and Provider Assessment of Lipid Management (PALM) Registry at the Duke Clinical Research Institute. Dr Virani has received research support or honoraria from the American Diabetes Association, the American Heart Association, World Heart Federation, the Veterans Affairs Health Services Research and Development Service, and the American College of Cardiology. Dr Krumholz has research agreements with Medtronic and Johnson & Johnson through his institution; is a member of the scientific advisory board for UnitedHealth; is a founder of Hugo; and is on advisory boards of IBM Watson and Element Science. All other authors have no relationships to disclose. No other disclosures were reported.

Figures

Figure.
Figure.. Cost-effectiveness Acceptability Curves at Different PCSK9i Prices With Permanent or Limited Patent Protection
Dotted lines signify permanent patent protection of proprotein convertase subtilisin/kexin type 9 inhibitor (PCSK9i) drugs, while solid lines signify patent protection that lapses after 12 years, leading to a 43% reduction in price.

Comment in

Similar articles

Cited by

References

    1. Sabatine MS, Giugliano RP, Keech AC, et al. ; FOURIER Steering Committee and Investigators . Evolocumab and clinical outcomes in patients with cardiovascular disease. N Engl J Med. 2017;376(18):1713-1722. - PubMed
    1. Kazi DS, Moran AE, Coxson PG, et al. . Cost-effectiveness of PCSK9 inhibitor therapy in patients with heterozygous familial hypercholesterolemia or atherosclerotic cardiovascular disease. JAMA. 2016;316(7):743-753. - PubMed
    1. Arrieta A, Page TF, Veledar E, Nasir K. Economic evaluation of PCSK9 inhibitors in reducing cardiovascular risk from health system and private payer perspectives. PLoS One. 2017;12(1):e0169761. - PMC - PubMed
    1. Fonarow GC, Keech AC, Pedersen TR, et al. . Cost-effectiveness of evolocumab therapy for reducing cardiovascular events in patients with atherosclerotic cardiovascular disease [published online August 23, 2017]. JAMA Cardiol. doi:10.1001/jamacardio.2017.2762 - DOI - PMC - PubMed
    1. Kazi DS, Penko J, Coxson PG, et al. . Updated cost-effectiveness analysis of PCSK9 inhibitors based on the results of the fourier trial. JAMA. 2017;318(8):748-750. - PMC - PubMed

MeSH terms

Substances