COMBINATION THERAPY;
VIRUS-INFECTION;
PLUS RIBAVIRIN;
RENAL-FUNCTION;
PHARMACOKINETICS;
PEGINTERFERON;
DOSAGE;
D O I:
10.1111/j.1365-2036.2009.04065.x
中图分类号:
R57 [消化系及腹部疾病];
学科分类号:
摘要:
P>Background The main goal of therapy in hepatitis C virus (HCV) infection is to achieve a sustained virological response (SVR). However, the impact of the pharmacological properties of ribavirin on the SVR has not been fully investigated. Aim To evaluate, through a prospective study, the association between ribavirin plasma level and SVR response in HCV patients treated with pegylated interferon (PEG-IFN) and ribavirin. Patients and methods Patients treated with PEG-IFN and ribavirin had plasmatic ribavirin dosage at weeks 4 and 12. SVR was evaluated 6 months after the end of treatment. Results At week 4, a strong correlation was found between HCV-RNA and C-min of ribavirin plasma level (r = -0.376, P = 0.002) and AUC(0 -> 12h) of ribavirin plasma level (r = -0.277, P = 0.018). At week 12, a strong correlation was found between HCV-RNA and C-min of ribavirin plasma level (r = -0.384, P < 0.0001) and AUC(0 -> 12h) of ribavirin plasma level (r = -0.257, P = 0.002). In genotype 1 patients, AUC(0 -> 12h) ribavirin and C-min were significantly correlated with negative HCV-RNA at week 12 and SVR. In the multiple logistic regression model, the only factor independently associated with SVR in genotype 1 patients was negative HCV-RNA at week 12. Conclusion C-min of ribavirin at weeks 4 and 12 was significantly higher in sustained virological responders compared with relapser or nonresponder patients. However, in genotype 1 patients, plasma ribavirin level at weeks 4 and 2 was not associated with SVR.