Assessing resistance costs of antiretroviral therapies via measures of future drug options

被引:24
作者
Jiang, HY
Deeks, SG
Kuritzkes, DR
Lallemant, M
Katzenstein, D
Albrecht, M
DeGruttola, V
机构
[1] Harvard Univ, Sch Publ Hlth, Dept Biostat, Stat & Data Anal Ctr, Boston, MA 02115 USA
[2] Inst Rech Dev, Res Unit 054, Paris, France
[3] Stanford Univ, Med Ctr, Stanford, CA 94305 USA
[4] Univ Calif San Francisco, Dept Med, San Francisco, CA USA
[5] San Francisco Gen Hosp, San Francisco, CA 94110 USA
[6] Beth Israel Deaconess Med Ctr, Boston, MA 02215 USA
[7] Harvard Univ, Harvard Med Sch, Div Aids, Boston, MA USA
[8] Harvard Univ, Brigham & Womens Hosp, Harvard Med Ctr, Sect Retroviral Therapeut, Boston, MA 02115 USA
关键词
D O I
10.1086/378355
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The emergence of drug-resistant human immunodeficiency virus (HIV) type 1 in the setting of antiretroviral therapy failure limits the number of drugs available for use in subsequent therapy regimens. To quantify the relative HIV-1-resistance costs associated with various antiretroviral therapy strategies, we developed 2 related measures of future drug options (FDOs) by use of rule-based genotype-interpretation systems. The FDO1 metric assesses the number of drug classes that remain useful; the FDO2 metric assesses the number of drug classes that remain useful and the number of active drugs within each class. Application of these methods is illustrated with data from a randomized study of 3 therapy regimens in nucleoside analog - experienced patients. Each therapy regimen resulted in a unique pattern of drug-resistance ( and cross-resistance) mutations. The regimen with the highest virologic failure rate preserved greater future drug options. Quantification of future drug options as an outcome of antiretroviral therapy trials may complement traditional clinical, virologic, and immunologic end points, thereby providing novel insights.
引用
收藏
页码:1001 / 1008
页数:8
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