Fuchs Edward J, Kiser Jennifer J, Hendrix Craig W, Sulkowski Mark, Radebaugh Christine, Bushman Lane, Ray Michelle L, Andrade Adriana
Department of Medicine, Johns Hopkins University, Baltimore, MD, USA.
Department of Pharmaceutical Sciences, University of Colorado Denver, Aurora, CO, USA.
J Antimicrob Chemother. 2016 Jun;71(6):1597-600. doi: 10.1093/jac/dkw009. Epub 2016 Feb 10.
The objective of this study was to evaluate the effects of abacavir on intracellular ribavirin triphosphate and plasma ribavirin trough concentrations.
Hepatitis C virus-infected subjects who had been cured or failed prior treatment were randomized to 8 weeks of ribavirin alone (N = 14; weight-based dosing) or weight-based ribavirin + abacavir (N = 14; 300 mg orally every 12 h). Ribavirin trough concentrations were measured on days 14, 28, 42 and 56; PBMCs for ribavirin triphosphate determination were sampled on days 28 and 56, pre-dose and at 6 and 12 h post-dose. ClinicalTrials.gov: NCT01052701.
Twenty-six subjects completed the study (24 males, 17 Caucasians, median age 52 years); 2 were excluded for missed pharmacokinetic visits. Fourteen subjects received ribavirin + abacavir and 12 received ribavirin alone. Mean ± SD plasma ribavirin trough concentrations (μg/mL) on days 14, 28, 42 and 56, respectively, were not significantly different with coadministration of abacavir (1.54 ± 0.60, 1.93 ± 0.54, 2.14 ± 0.73 and 2.54 ± 1.05) compared with ribavirin alone (1.48 ± 0.32, 2.08 ± 0.41, 2.32 ± 0.47 and 2.60 ± 0.62) (P > 0.40). Mean ribavirin triphosphate intracellular concentrations (pmol/10(6) cells) on days 28 and 56, respectively, did not differ statistically between abacavir users (11.98 ± 9.86 and 15.87 ± 12.52) and non-users (15.91 ± 15.58 and 15.93 ± 12.69) (P > 0.4). Adverse events were mild or moderate, except for three grade 3 occurrences of transaminitis, cholecystitis and low absolute neutrophil count that resolved and were judged not attributable to study medications.
Abacavir did not significantly alter ribavirin or ribavirin triphosphate concentrations.
本研究的目的是评估阿巴卡韦对细胞内三磷酸利巴韦林及血浆利巴韦林谷浓度的影响。
将之前治疗已治愈或失败的丙型肝炎病毒感染受试者随机分为两组,一组单独使用利巴韦林8周(N = 14;基于体重给药),另一组使用基于体重的利巴韦林+阿巴卡韦(N = 14;每12小时口服300 mg)。在第14、28、42和56天测量利巴韦林谷浓度;在第28和56天,给药前以及给药后6小时和12小时采集外周血单核细胞用于测定三磷酸利巴韦林。ClinicalTrials.gov:NCT01052701。
26名受试者完成了研究(24名男性,17名高加索人,中位年龄52岁);2名受试者因错过药代动力学访视而被排除。14名受试者接受了利巴韦林+阿巴卡韦,12名受试者单独接受了利巴韦林。与单独使用利巴韦林相比,在第14、28、42和56天,阿巴卡韦联合使用时的平均±标准差血浆利巴韦林谷浓度(μg/mL)分别为(1.54±0.60、1.93±0.54、2.14±0.73和2.54±1. (P>0.40)。在第28和56天,阿巴卡韦使用者(11.98±9.86和15.87±12.52)与非使用者(15.91±15.58和15.93±12.69)之间的平均三磷酸利巴韦林细胞内浓度(pmol/10(6)细胞)在统计学上无差异(P>0.4)。不良事件为轻度或中度,除了3例3级转氨酶升高、胆囊炎和绝对中性粒细胞计数降低事件,这些事件均已缓解且判定与研究药物无关。
阿巴卡韦未显著改变利巴韦林或三磷酸利巴韦林的浓度。