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

机译:通用泛肠道基因型Sofosbuvir / Velpatasvir与基因型依赖性直效抗病毒的成本效益,用于丙型肝炎治疗方法

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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.
机译:背景和AIM治疗印度和其他发展中国家可用的低成本通用直效抗病毒(DAAS)的丙型肝炎病毒(HCV)感染需要测定HCV基因型(“基因型依赖性”方案)。通用VelpataSvir,消除了对基因型测定的需要(“泛基因型”方案),最近变得可用,但是昂贵的。本研究的目的是评估基因型依赖性与印度泛基因型DAA治疗的成本效益。方法采用先前经过先前验证的微仿模型,适用于印度人群,用于比较三种情况的成本和长期结果:无治疗,与基因型依赖的方案治疗,以及泛基因型方案治疗。输入参数来自文献。计算了Payer的透视和终身时间范围,计算了质量调整的寿命年(qalys),总成本和增量成本效益比。还进行了确定性和概率敏感性分析。结果目前的价格(4周持续4周),泛基因型方案与没有治疗相比是节省成本节省的。与基因型依赖的方案相比,Qalys增加了0.92,增加了成本,每107美元,但被认为是成本效益,增量成本效益比率为每股QALY为242美元。概率敏感性分析还支持泛基因型方案的成本效益。在4周的价格下降4周的价格降低,泛基因型方案将变得成本中性与基因型依赖的方案(当前价格:US100持续4周)。结论目前,基于VelpataSvir的Pan-Genotypic方案对于印度的HCV治疗具有成本效益,其中可用的药物。泛基因型方案的价格降低有可能使其使用成本节省成本,同时简化了针对HCV消除的社区级计划的治疗。

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