Cost-effectiveness of CYP2B6 genotyping to optimize efavirenz dosing in HIV clinical practice

被引:16
作者
Schackman, Bruce R. [1 ]
Haas, David W. [2 ]
Park, Sanghee S. [3 ]
Li, X. Cynthia [3 ]
Freedberg, Kenneth A. [3 ,4 ,5 ]
机构
[1] Weill Cornell Med Coll, Dept Healthcare Policy & Res, New York, NY 10065 USA
[2] Vanderbilt Univ, Sch Med, Dept Med, Div Infect Dis, Nashville, TN 37212 USA
[3] Massachusetts Gen Hosp, Med Practice Evaluat Ctr, Div Gen Internal Med, Boston, MA 02114 USA
[4] Massachusetts Gen Hosp, Div Infect Dis, Boston, MA 02114 USA
[5] Harvard TH Chan Sch Publ Hlth, Dept Hlth Policy & Management, Boston, MA USA
关键词
antiretroviral therapy; cost-effectiveness; dose optimization; genotyping; HIV; INITIAL ANTIRETROVIRAL THERAPY; PLASMA-CONCENTRATIONS; DOSE REDUCTION; DOUBLE-BLIND; REGIMENS; PHARMACOKINETICS; POLYMORPHISMS; COMBINATION; METABOLISM; INFECTION;
D O I
10.2217/pgs.15.142
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
To assess the cost-effectiveness of CYP2B6 genotyping to guide efavirenz dosing for initial HIV therapy in the USA. Methods: We used the Cost-Effectiveness of Preventing AIDS Complications (CEPAC) microsimulation model to project quality-adjusted life expectancy and lifetime costs (2014 US dollars) for efavirenz-based HIV therapy with or without CYP2B6 genotyping. We assumed that with genotyping 60% of patients would be eligible to receive lower doses. Results: Current care without CYP2B6 genotyping has an incremental cost-effectiveness ratio >$100,000/QALY compared with genotype-guided dosing, even if lower dosing reduces efficacy. When we assumed generic efavirenz availability, conclusions were similar unless lower dosing reduces efficacy by 6% or more. Conclusion: CYP2B6 genotyping can inform efavirenz dosing and decrease HIV therapy cost.
引用
收藏
页码:2007 / 2018
页数:12
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