Cost-effectiveness of PCSK9 inhibition in addition to standard lipid-lowering therapy in patients at high risk for vascular disease. (15th February 2018)

• Record Type: Journal Article
• Authors: Stam-Slob, Manon C.; van der Graaf, Yolanda; de Boer, Anthonius; Greving, Jacoba P.; Visseren, Frank L.J.
• Is Part Of: International journal of cardiology. Volume 253(2018)
• Page Start: 148
• Page End: 154
• Publication Date: 2018-02-15
• Subjects: Cost-effectiveness -- PCSK9 inhibition -- Lifetime benefit -- (Quality-adjusted) life years -- Vascular disease; Cardiology -- Periodicals; Electronic journals; 616.12
• DOI: 10.1016/j.ijcard.2017.10.080
• Languages: English
• ISSNs: 0167-5273

Abstract

Abstract: Background: As proprotein convertase subtilisin-kexin type 9 (PCSK9) monoclonal antibodies are entering the market, we assessed the cost-effectiveness of PCSK9 inhibition added to standard lipid-lowering therapy in patient groups at high risk for major adverse cardiovascular events (MACE). Methods: A lifetime Markov Model was designed to estimate healthcare costs, quality-adjusted life years (QALYs) and incremental cost-effectiveness ratios (ICERs) for PCSK9 inhibition added to standard therapy in patients with Familial Hypercholesterolemia (FH), patients with vascular disease at high MACE recurrence risk, and patients with vascular disease with diabetes mellitus. The balance between costs and health outcomes was established for a broad range of potential relative risk reductions and drug costs. Results: The expected QALY gain per patient and ICER in the main scenario were 1.4 QALYs for €78, 485/QALY gained in patients with FH, 0.22 QALYs for €176, 735/QALY gained in those with vascular disease and a predicted risk of MACE ≥ 30% in 10 years, and 0.22 QALYs for €295, 543/QALY gained in those with vascular disease and diabetes. Results were sensitive to assumptions on PCSK9 inhibitor treatment efficacy, and vascular event risks. Conclusion: The costs and effects of PCSK9 inhibition added to standard lipid-lowering treatment in patient groups at high risk for MACE can be estimated and adapted to a specific clinical setting. PCSK9 inhibition could be cost-effective in patients with FH. In patients with vascular disease PCSK9 inhibition is less cost-effective, however, a price development may change clinical practice. This model may aid treatment and reimbursement decisions regarding PCSK9 inhibitors.