Amorosa Valerianna K, Slim Jihad, Mounzer Karam, Bruno Christopher, Hoffman-Terry Margaret, Dorey-Stein Zachariah, Ferrara Thomas, Kostman Jay R, Lo Re Vincent
Division of Infectious Diseases, Department of Medicine, University of Pennsylvania School of Medicine, Philadelphia, PA, USA.
Antivir Ther. 2010;15(1):91-9. doi: 10.3851/IMP1492.
It remains unclear if certain antiretroviral medications, particularly abacavir, compromise response to HCV therapy. Such data could inform the selection of appropriate antiretrovirals in HIV/HCV-coinfected patients. The aim of this study was to determine if use of abacavir, as well as other antiretrovirals, was associated with reduced response to pegylated interferon (PEG-IFN) plus ribavirin.
A cohort study was performed among antiretroviral-treated HIV/HCV-coinfected patients initiating PEG-IFN plus ribavirin between January 2001 and June 2007 at six sites in the United States. Abacavir and other antiretrovirals represented exposures of interest. Study outcomes included an early virological response (> or =2 log IU/ml decrease in HCV viral load at 12 weeks) and sustained virological response (undetectable HCV viral load 24 weeks after treatment discontinuation).
Among 212 patients, 74 (35%) received abacavir. For patients infected with HCV genotype 1 or 4, no differences were observed between abacavir users and non-users in early virological response (26 [40%] versus 53 [44%]; adjusted odds ratio [OR] 1.00; 95% confidence interval [CI] 0.50-2.00) or sustained virological response (8 [13%] versus 13 [12%]; adjusted OR 1.34; 95% CI 0.50-3.62). Among genotype 2 and 3 patients, rates of early virological response (7 [78%] versus 16 [89%]; OR 0.44; 95% CI 0.05-3.76) and sustained virological response (3 [33%] versus 8 [44%]; OR 0.63; 95% CI 0.12-3.32) were also similar between abacavir users and non-users. No association was found between other antiretrovirals and a lack of early or sustained response.
Use of abacavir or other antiretroviral medications was not associated with reduced early or sustained virological response rates.
目前尚不清楚某些抗逆转录病毒药物,尤其是阿巴卡韦,是否会影响丙型肝炎病毒(HCV)治疗的反应。此类数据可为HIV/HCV合并感染患者选择合适的抗逆转录病毒药物提供参考。本研究的目的是确定使用阿巴卡韦以及其他抗逆转录病毒药物是否与聚乙二醇干扰素(PEG-IFN)联合利巴韦林治疗反应降低有关。
对2001年1月至2007年6月期间在美国六个地点开始接受PEG-IFN联合利巴韦林治疗的抗逆转录病毒治疗的HIV/HCV合并感染患者进行了一项队列研究。阿巴卡韦和其他抗逆转录病毒药物为感兴趣的暴露因素。研究结局包括早期病毒学反应(治疗12周时HCV病毒载量下降≥2 log IU/ml)和持续病毒学反应(停药24周后HCV病毒载量不可检测)。
在212例患者中,74例(35%)接受了阿巴卡韦治疗。对于感染HCV 1型或4型的患者,阿巴卡韦使用者和非使用者在早期病毒学反应(26例[40%]对53例[44%];调整优势比[OR]为1.00;95%置信区间[CI]为0.50 - 2.00)或持续病毒学反应(8例[13%]对13例[12%];调整OR为1.34;CI为0.50 - 3.62)方面未观察到差异。在2型和3型患者中,阿巴卡韦使用者和非使用者的早期病毒学反应率(7例[78%]对16例[89%];OR为0.44;95% CI为0.05 - 3.76)和持续病毒学反应率(3例[33%]对8例[44%];OR为0.63;95% CI为0.12 - 3.32)也相似。未发现其他抗逆转录病毒药物与早期或持续反应缺乏之间存在关联。
使用阿巴卡韦或其他抗逆转录病毒药物与早期或持续病毒学反应率降低无关。