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用于治疗杂合子家族性高胆固醇血症或有临床动脉粥样硬化性心血管疾病的成年患者的 PCSK9 抑制剂的预算影响分析。

Budget Impact Analysis of PCSK9 Inhibitors for the Management of Adult Patients with Heterozygous Familial Hypercholesterolemia or Clinical Atherosclerotic Cardiovascular Disease.

机构信息

Sanofi US, Bridgewater, NJ, USA.

Regeneron Pharmaceuticals, Inc., Tarrytown, NY, USA.

出版信息

Pharmacoeconomics. 2018 Jan;36(1):115-126. doi: 10.1007/s40273-017-0590-5.

Abstract

OBJECTIVE

The aim of this study was to assess the budget impact of introducing the proprotein convertase subtilisin/kexin type 9 inhibitors (PCSK9i) alirocumab and evolocumab to market for the treatment of adults with heterozygous familial hypercholesterolemia or clinical atherosclerotic cardiovascular (CV) disease requiring additional lowering of low-density lipoprotein cholesterol (LDL-C).

METHODS

A 3-year model estimated the costs of lipid-modifying therapy (LMT) and CV events to a hypothetical US health plan of 1 million members, comparing two scenarios-with and without the availability of PCSK9i as add-on therapy to statins. Proportions of patients with uncontrolled LDL-C despite receiving statins, and at risk of CV events, were estimated from real-world data. Total undiscounted annual LMT costs (2017 prices, including PCSK9i costs of $14,563.50), dispensing and healthcare costs, including the costs of CV events, were estimated for all prevalent patients in the target population, based on baseline risk factors. Maximum PCSK9i utilization of 1-5% over 3 years according to risk group (following the same pattern as current ezetimibe use), and 5-10% as a secondary scenario, were assumed.

RESULTS

Total healthcare budget impacts per target patient (and per member) per month for years 1, 2 and 3 were $3.62($0.10), $7.22($0.20) and $10.79($0.30), respectively, assuming 1-5% maximum PCSK9i utilization, and $15.81($0.44), $31.52($0.88) and $47.12($1.31), respectively, assuming 5-10% utilization. Results were sensitive to changes in model timeframe, years to maximum PCSK9i utilization and PCSK9i costs.

CONCLUSIONS

The budget impact of PCSK9i as add-on therapy to statins for patients with hypercholesterolemia is relatively low compared with published estimates for other specialty biologics. Drug cost rebates and discounts are likely to further reduce budget impact.

摘要

目的

本研究旨在评估将前蛋白转化酶枯草溶菌素/克那霉 9 抑制剂(PCSK9i)阿利罗库单抗和依洛尤单抗引入市场用于治疗杂合子家族性高胆固醇血症或需要进一步降低低密度脂蛋白胆固醇(LDL-C)的临床动脉粥样硬化性心血管(CV)疾病的成年患者的预算影响。

方法

一个为期 3 年的模型估计了一个拥有 100 万成员的美国健康计划中调脂治疗(LMT)和 CV 事件的成本,比较了两种情况:是否有 PCSK9i 作为他汀类药物的附加治疗。从真实世界的数据中估计了尽管接受他汀类药物治疗但 LDL-C 仍不受控制且有发生 CV 事件风险的患者比例。根据基线风险因素,对目标人群中所有现患患者的未贴现年度 LMT 总成本(2017 年价格,包括 PCSK9i 费用 14563.50 美元)、配药和医疗保健费用(包括 CV 事件成本)进行了估计。假设在 3 年内根据风险组(遵循与当前依泽替米贝相同的模式)最大利用 1-5%的 PCSK9i,以及作为次要方案利用 5-10%的 PCSK9i。

结果

假设最大利用 1-5%的 PCSK9i,每年 1、2 和 3 个月每位目标患者(每位成员)的总医疗保健预算影响分别为 3.62 美元(0.10 美元)、7.22 美元(0.20 美元)和 10.79 美元(0.30 美元);假设最大利用 5-10%的 PCSK9i,每年 1、2 和 3 个月每位目标患者(每位成员)的总医疗保健预算影响分别为 15.81 美元(0.44 美元)、31.52 美元(0.88 美元)和 47.12 美元(1.31 美元)。结果对模型时间范围、达到 PCSK9i 最大利用的时间和 PCSK9i 成本的变化敏感。

结论

与其他专科生物制剂的已发表估计相比,PCSK9i 作为他汀类药物的附加治疗用于治疗高胆固醇血症患者的预算影响相对较低。药物回扣和折扣可能会进一步降低预算影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dd71/5775395/7727d5a7d9f4/40273_2017_590_Fig1_HTML.jpg

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