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Randomized Trial Evaluating the Impact of Ribavirin Mono-Therapy and Double Dosing on Viral Kinetics Ribavirin Pharmacokinetics and Anemia in Hepatitis C Virus Genotype 1 Infection

机译:评估利巴韦林单药和双剂量对丙型肝炎病毒基因型1感染病毒动力学利巴韦林药代动力学和贫血的影响的随机试验。

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摘要

In this pilot study (RibaC), 58 hepatitis C virus (HCV) genotype 1 infected treatment-naïve patients were randomized to (i) 2 weeks ribavirin double dosing concomitant with pegylated interferon-α (pegIFN-α), (ii) 4 weeks ribavirin mono-therapy prior to adding pegIFN-α, or (iii) standard-of-care (SOC) ribavirin dosing concurrent with pegIFN-α. Four weeks of ribavirin mono-therapy resulted in a mean 0.46 log10 IU/mL HCV RNA reduction differentially regulated across IL28B genotypes (0.89 vs. 0.21 log10 IU/mL for CC and CT/TT respectively; P = 0.006), increased likelihood of undetectable HCV RNA week 4 after initiating pegIFN-α and thus shortened treatment duration (P<0.05), and decreased median IP-10 concentration from 550 to 345 pg/mL (P<0.001). Both experimental strategies impacted on ribavirin concentrations, and high levels were achieved after one week of double dosing. However, by day 14, double dosing entailed a greater hemoglobin decline as compared to SOC (2.2 vs. 1.4 g/dL; P = 0.03). Conclusion: Ribavirin down-regulates IP-10, and may have an anti-viral effect differently regulated across IL28B genotypes.Trial RegistrationClinicalTrials.gov
机译:在这项前瞻性研究(RibaC)中,将58位感染了基因型1的未感染丙型肝炎病毒(HCV)的患者随机分为(i)2周联合利巴韦林与聚乙二醇干扰素-α(pegIFN-α)联合给药,(ii)4周利巴韦林单药治疗,然后添加pegIFN-α,或(iii)利巴韦林与pegIFN-α同时给药。利巴韦林单药治疗四周导致IL28B基因型差异平均调节0.46 log10 IU / mL HCV RNA减少(CC和CT / TT分别为0.89对0.21 log10 IU / mL; P = 0.006),无法检测的可能性增加HCV RNA在启动pegIFN-α后第4周,因此缩短了治疗时间(P <0.05),并使IP-10的中位浓度从550 pg / mL降低到345 pg / mL(P <0.001)。两种实验策略均影响利巴韦林的浓度,并且在双剂量一周后达到了高水平。但是,到第14天,与SOC相比,双剂量给药使血红蛋白下降幅度更大(2.2 vs. 1.4 g / dL; P = 0.03)。结论:利巴韦林下调IP-10,并且可能在IL28B基因型之间具有不同的抗病毒作用。

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