Department of Health Policy and Management, Robert Stempel College of Public Health and Social Work, Florida International University, Miami.
Department of Health Policy and Management, Johns Hopkins Bloomberg School of Public Health, Johns Hopkins University, Baltimore, Maryland.
JAMA Cardiol. 2017 Dec 1;2(12):1369-1374. doi: 10.1001/jamacardio.2017.3655.
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.
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.
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.
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.
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.
先前关于前蛋白转化酶枯草溶菌素/克那霉 9 抑制剂(PCSK9i)的成本效益初步分析是基于 PCSK9i 试验中降低低密度脂蛋白胆固醇的获益估计得出的,这些获益在不同的试验中存在差异。最近的进一步心血管结局研究中 PCSK9 抑制剂在高危患者中的应用(FOURIER 试验)提供了关于该药物有效性的更好信息。
利用试验结果来确定与单独使用他汀类药物相比,PCSK9i 和他汀类药物联合治疗策略的成本效益。
设计、环境和参与者:我们从现有文献中获得了一个类似于 FOURIER PCSK9i 试验人群的理论队列的事件、结局、护理成本和医疗保险费用的观察率,并在整个生命周期内创建了一个 Markov 模型。
我们从卫生系统的角度评估了增量成本效益比,从私人支付者的角度评估了投资回报。对于这两个指标,我们假设 PCSK9i 药物的年价格为 14300 美元,在美国专利保护失效后的第 12 年,价格将降低 43%。成本以 2016 年的美元计价。
本研究对 1000 名具有与 FOURIER 试验队列相似特征的假设患者进行了建模。在目前的价格下,他汀类药物加 PCSK9i 治疗的增量成本效益比为每质量调整生命年 337729 美元。我们的概率敏感性分析发现,在通常接受的每质量调整生命年 10 万美元的社会阈值下,他汀类药物加 PCSK9i 治疗策略的成本效益可能性较低(<1%)。此外,私人支付者使用 PCSK9i 的投资回报率为负 86%。在我们的阈值分析中,PCSK9i 的价格需要下降 62%,降至每年 5459 美元,才能达到每质量调整生命年 10 万美元。
在目前的价格下,PCSK9i 联合他汀类药物治疗估计每增加 1 个质量调整生命年需要花费 337729 美元。需要大幅度降价才能达到传统的成本效益标准。