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通用泛基因型索磷布韦/维帕他韦与基于基因型的直接作用抗病毒药物治疗丙型肝炎的成本效益比较。

Cost-effectiveness of generic pan-genotypic sofosbuvir/velpatasvir versus genotype-dependent direct-acting antivirals for hepatitis C treatment.

机构信息

Department of Gastroenterology, Sanjay Gandhi Postgraduate Institute of Medical Sciences, Lucknow, India.

Harold and Inge Marcus Department of Industrial and Manufacturing Engineering, Penn State University, State College, Pennsylvania, USA.

出版信息

J Gastroenterol Hepatol. 2018 Dec;33(12):2029-2036. doi: 10.1111/jgh.14301. Epub 2018 Jun 25.

Abstract

BACKGROUND AND AIM

Treatment of hepatitis C virus (HCV) infection with low-cost generic direct-acting antivirals (DAAs) available in India and other developing countries needs determination of HCV genotype ("genotype-dependent" regimens). Generic velpatasvir, a DAA that obviates the need for genotype determination ("pan-genotypic" regimen), recently became available but is costlier. The aim of this study was to evaluate the cost-effectiveness of genotype-dependent versus pan-genotypic DAA treatments in India.

METHODS

A previously validated microsimulation model, adapted to Indian population, was used to compare the costs and long-term outcomes of three scenarios: no treatment, treatment with genotype-dependent regimens, and treatment with pan-genotypic regimen. Input parameters were derived from literature. Using a payer's perspective and lifetime time horizon, quality-adjusted life-years (QALYs), total costs, and incremental cost-effectiveness ratio were calculated. Both deterministic and probabilistic sensitivity analyses were also conducted.

RESULTS

At the current price ($US223 for 4 weeks), pan-genotypic regimen was cost-saving compared with no treatment. Compared with genotype-dependent regimens, it increased QALYs by 0.92 and increased costs by $US107 but was deemed cost-effective with an incremental cost-effectiveness ratio of $US242 per QALY gained. Probabilistic sensitivity analysis also supported the cost-effectiveness of pan-genotypic regimen. At the reduced price of $US188 for 4 weeks, the pan-genotypic regimen will become cost-neutral to genotype-dependent regimens (current price: $US100 for 4 weeks).

CONCLUSIONS

At current prices, velpatasvir-based pan-genotypic regimen is cost-effective for HCV treatment in India where generic drugs are available. A reduction in the prices of pan-genotypic regimen has the potential to make its use cost-saving while simplifying treatment in community-level programs aimed at HCV elimination.

摘要

背景和目的

在印度和其他发展中国家,使用低成本的通用直接作用抗病毒药物(DAAs)治疗丙型肝炎病毒(HCV)感染需要确定 HCV 基因型(“基因型依赖性”方案)。通用伏拉帕他韦是一种无需确定基因型的 DAAs(“泛基因型”方案),最近已上市,但价格更高。本研究旨在评估印度基因型依赖性与泛基因型 DAA 治疗的成本效益。

方法

使用先前验证的微模拟模型,适用于印度人群,比较三种方案的成本和长期结果:不治疗、基因型依赖性方案治疗和泛基因型方案治疗。输入参数来自文献。采用支付者的观点和终生时间范围,计算了质量调整生命年(QALYs)、总费用和增量成本效益比。还进行了确定性和概率敏感性分析。

结果

在当前价格(4 周 223 美元)下,与不治疗相比,泛基因型方案具有成本效益。与基因型依赖性方案相比,它增加了 0.92 个 QALYs,并增加了 107 美元的成本,但被认为具有成本效益,增量成本效益比为每获得一个 QALY 增加 242 美元。概率敏感性分析也支持泛基因型方案的成本效益。在 4 周 188 美元的降价下,泛基因型方案将与基因型依赖性方案持平(目前价格:4 周 100 美元)。

结论

在当前价格下,基于伏拉帕他韦的泛基因型方案在印度治疗 HCV 具有成本效益,印度有通用药物。降低泛基因型方案的价格有可能使其在简化旨在消除 HCV 的社区级项目中的治疗的同时具有成本效益。

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