作者: E. S. A. Araújo , H. Dahari , A. U. Neumann , N. de Paula Cavalheiro , C. E. Melo
DOI: 10.1111/J.1365-2893.2010.01358.X
关键词:
摘要: Summary. The objective of this study was to find very early viral kinetic markers predict nonresponse hepatitis C virus (HCV) therapy in a group human immunodeficiency (HIV)/HCV-coinfected patients. Twenty-six patients (15 HCV genotype-1 and 11 genotype-3) were treated with 48-week regimen peginterferon-alfa-2a (PEG-IFN) (180 μg/week) weight-based ribavirin (11 mg/kg/day). Samples collected at baseline; 4, 8, 12, 18, 24, 30, 36 42 h; days 2, 3, 7, 15, 22, 29, 43 57 then weekly monthly. Five discontinued treatment. Seven (27%) achieved sustained virological response (SVR). Nadir RNA levels observed 1.6 ± 0.3 days after initiation therapy, followed by 0.3- 12.9-fold rebound until the administration second dose PEG-IFN, which not associated SVR or genotype. A decline <1.19 log for <0.97 log genotype-3, 2 days starting had negative predictive value (NPV) 100% SVR. day 2 similar positive as rapid week 4. In addition, second-phase slope (i.e., measured from 29) <0.3 log/week NPV = 100% We conclude that first-phase (<0.3 log/week) are excellent predictors nonresponse. Further studies needed validate these parameters on-treatment prognosticators HIV.