Suppr超能文献

丙型肝炎病毒的早期治疗:从意大利的角度来看,这是一个具有成本效益的选择吗?

Early Treatment in HCV: Is it a Cost-Utility Option from the Italian Perspective?

作者信息

Marcellusi Andrea, Viti Raffaella, Damele Francesco, Cammà Calogero, Taliani Gloria, Mennini Francesco Saverio

机构信息

National Research Council (CNR), Institute for Research on Population and Social Policies (IRPPS), Rome, Italy.

Economic Evaluation and HTA (CEIS-EEHTA)-IGF Department, Faculty of Economics, University of Rome "Tor Vergata", Rome, Italy.

出版信息

Clin Drug Investig. 2016 Aug;36(8):661-72. doi: 10.1007/s40261-016-0414-y.

Abstract

BACKGROUND AND OBJECTIVE

In Italy, the Italian Pharmaceutical Agency (AIFA) criteria used F3-F4 fibrosis stages as the threshold to prioritise the treatment with interferon (IFN)-free regimens, while in genotype 1 chronic hepatitis C (G1 CHC) patients with fibrosis of liver stage 2, an approach with pegylated interferon (PEG-IFN)-based triple therapy with simeprevir was suggested. The key clinical question is whether, in an era of financial constraints, the application of a universal IFN-free strategy in naïve G1 CHC patients is feasible within a short time horizon. The aim of this study is to perform an economic analysis to estimate the cost-utility of the early innovative therapy in Italy for managing hepatitis C virus (HCV)-infected patients.

METHODS

The incremental cost-utility analysis was carried out to quantify the benefits of the early treatment approach in HCV subjects. A Markov simulation model including direct and indirect costs and health outcomes was developed from an Italian National Healthcare Service and societal perspective. A total of 5000 Monte Carlo simulations were performed on two distinct scenarios: standard of care (SoC) which includes 14,000 genotype 1 patients in Italy treated with innovative interferon-free regimens in the fibrosis of liver stages 3 and 4 (F3-F4) versus early-treatment scenario (ETS) where 2000 patients were additionally treated with simeprevir plus PEG-IFN and ribavirin in the fibrosis stage 2 (F2) (based on Italian Medicines Agency AIFA reimbursement criteria). A systematic literature review was carried out to identify epidemiological and economic data, which were subsequently used to inform the model. Furthermore, a one-way probabilistic sensitivity was performed to measure the relationship between the main parameters of the model and the cost-utility results.

RESULTS

The model shows that, in terms of incremental cost-effectiveness ratio (ICER) per quality adjusted life year (QALY) gained, ETS appeared to be the most cost-utility option compared with both perspective societal (ICER = EUR11,396) and NHS (ICER = EUR14,733) over a time period of 10 years. The cost-utility of ETS is more sustainable as it extends the time period analysis [ICER = EUR 6778 per QALY to 20 years and EUR4474 per QALY to 30 years]. From the societal perspective, the ETS represents the dominant option at a time horizon of 30 years. If we consider the sub-group population of treated patients [16,000 patients of which 2000 not treated in the SoC, the ETS scenario was dominant after only 5 years and the cost-utility at 2 years of simulation. The one-way sensitivity analysis on the main variables confirmed the robustness of the model for the early-treatment approach.

CONCLUSION

Our model represents a tool for policy makers and health-care professionals, and provided information on the cost-utility of the early-treatment approach in HCV-infected patients in Italy. Starting innovative treatment regimens earlier keeps HCV-infected patients in better health and reduces the incidence of HCV-related events; generating a gain both in terms of health of the patients and correct resource allocation.

摘要

背景与目的

在意大利,意大利药品管理局(AIFA)的标准将F3 - F4纤维化阶段作为优先使用无干扰素方案进行治疗的阈值,而对于肝纤维化2期的基因1型慢性丙型肝炎(G1 CHC)患者,建议采用基于聚乙二醇干扰素(PEG - IFN)联合simeprevir的三联疗法。关键临床问题是,在财政紧张的时代,对初治G1 CHC患者应用通用的无干扰素策略在短时间内是否可行。本研究的目的是进行一项经济分析,以估计意大利早期创新疗法治疗丙型肝炎病毒(HCV)感染患者的成本效用。

方法

进行增量成本效用分析,以量化HCV患者早期治疗方法的益处。从意大利国家医疗服务体系和社会角度出发,开发了一个包含直接和间接成本以及健康结果的马尔可夫模拟模型。在两种不同情景下共进行了5000次蒙特卡洛模拟:标准治疗(SoC)情景,包括意大利14000例基因1型患者,在肝纤维化3期和4期(F3 - F4)接受创新的无干扰素方案治疗;早期治疗情景(ETS),额外有2000例患者在纤维化2期(F2)接受simeprevir联合PEG - IFN和利巴韦林治疗(基于意大利药品管理局AIFA的报销标准)。进行了系统的文献综述以确定流行病学和经济数据,随后将其用于模型构建。此外,进行了单向概率敏感性分析,以衡量模型主要参数与成本效用结果之间的关系。

结果

模型显示,就每获得一个质量调整生命年(QALY)的增量成本效益比(ICER)而言,在10年期间,与社会视角(ICER = 11396欧元)和国民医疗服务体系(NHS,ICER = 14733欧元)相比,ETS似乎是最具成本效用的选择。ETS的成本效用更具可持续性,因为随着分析时间延长,其ICER在20年时为每QALY 6778欧元,在30年时为每QALY 4474欧元。从社会角度看,在30年的时间范围内,ETS是占优选择。如果考虑治疗患者的亚组人群(共16000例患者,其中2000例在SoC情景中未接受治疗),在模拟2年时,ETS情景在仅5年后就占优,且具有成本效用。对主要变量的单向敏感性分析证实了早期治疗方法模型的稳健性。

结论

我们的模型为政策制定者和医疗保健专业人员提供了一个工具,并提供了关于意大利HCV感染患者早期治疗方法成本效用的信息。更早开始创新治疗方案可使HCV感染患者保持更好的健康状态,并降低HCV相关事件的发生率;在患者健康和正确的资源分配方面都能带来益处。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验