Cost-effectiveness of IL28Β genotype-guided protease inhibitor triple therapy versus standard of care treatment in patients with hepatitis C genotypes 2 or 3 infection.
Cost-effectiveness of IL28Β genotype-guided protease inhibitor triple therapy versus standard of care treatment in patients with hepatitis C genotypes 2 or 3 infection.
复制标题
IL28α 基因型引导的蛋白酶抑制剂三联疗法与丙型肝炎基因型 2 或 3 感染患者标准护理治疗的成本效益。
DOI:
10.1159/000365939
复制
发表时间:
2014
影响因子:
1.7
通讯作者:
Williams,MarcS
中科院分区:
文献类型:
--
作者:
Bock,JonathanA;Fairley,KimberlyJ;Smith,RobertE;Maeng,DanielD;Pitcavage,JamesM;Inverso,NicholasA;Williams,MarcS
Background/Aims:Triple therapy [adding protease inhibitors to standard of care (SOC)] dramatically increases treatment response in selected patients with hepatitis C virus (HCV). Interleukin 28B(IL28Β)genotyping helps predict responsiveness in these patients; however, the economic implications ofIL28Βgenotyping in HCV genotype 2 or 3 infected patients are unknown. Short- and long-term costs and outcomes of SOC therapy were calculated and used to determine the cost-effectiveness thresholds for using triple therapy in HCV genotype 2 or 3 infected patients.Methods:Costs and outcomes were calculated by conducting cohort simulations on decision trees modeling SOC and triple therapy. Quality-adjusted life expectancies and long-term costs were predicted through Markov modeling.Results:For triple therapy to be cost-effective, sustained virologic response (SVR) rates must improve (depending on age) by 7.91-11.11 and 9.06-12.8% for HCV genotype 2 and 3 cohorts, respectively. When triple therapy is guided by 2IL28Βvariants, a 2.63-3.72% improvement in SVR is needed for cost-effectiveness, and when guided by only one variant, a 1.4-8.91% improvement is needed.Conclusions:Markov modeling revealed that modest increases in SVR rates fromIL28Β-guided triple therapy can lead to both lower costs and better health outcomes than SOC therapy in the long run.