D'Avolio Antonio, Cusato Jessica, De Nicolò Amedeo, Allegra Sarah, Di Perri Giovanni
Unit of Infectious Diseases, Department of Medical Sciences, Amedeo di Savoia Hospital, University of Turin, Turin, Italy.
Pharmacogenomics. 2016 Jun;17(8):925-41. doi: 10.2217/pgs.16.22. Epub 2016 Jun 1.
Dual therapy (pegylated interferon plus ribavirin) was considered the standard of care for hepatitis C virus (HCV) treatment until 2011, when the first-wave direct-acting antivirals were added to this regimen for HCV genotype-1 patients to increase the sustained virological response rate. The second-wave direct-acting antivirals entered the clinical use also in some ribavirin (RBV)- and/or interferon-free combinations. Nevertheless, since some of the new therapeutic regimens also include RBV and its use results still associated with hemolytic anemia, this requires countermeasures to be prevented. These include the identification of several host predictive factors involved in RBV absorption, distribution, metabolism, elimination and many others that might influence this toxic effect. For this reason, we provided an overview of the potential role of pharmacogenomics in predisposing RBV-treated HCV patients to anemia.
在2011年之前,双重疗法(聚乙二醇化干扰素加利巴韦林)一直被视为丙型肝炎病毒(HCV)治疗的标准疗法。2011年,第一代直接作用抗病毒药物被添加到该治疗方案中,用于治疗HCV基因1型患者,以提高持续病毒学应答率。第二代直接作用抗病毒药物也以一些不含利巴韦林(RBV)和/或干扰素的联合用药形式进入临床使用。然而,由于一些新的治疗方案中仍包含RBV,且其使用结果仍与溶血性贫血相关,因此需要采取对策来预防。这些对策包括识别一些参与RBV吸收、分布、代谢、消除以及其他可能影响这种毒性作用的宿主预测因素。出于这个原因,我们概述了药物基因组学在使接受RBV治疗的HCV患者易患贫血方面的潜在作用。