Corti Giampaolo, Salomoni Elena, Baragli Filippo
Infectious Disease Unit, Department of Experimental and Clinical Medicine, University of Florence School of Medicine, Largo Brambilla 3, I-50134 Florence, Italy.
Infectious Disease Unit, Department of Experimental and Clinical Medicine, University of Florence School of Medicine, Largo Brambilla 3, I-50134 Florence, Italy.
Int J Infect Dis. 2014 Feb;19:85-6. doi: 10.1016/j.ijid.2013.09.002. Epub 2013 Oct 25.
The recent introduction of direct antiviral agents (DAAs) as a fundamental part of anti-hepatitis C virus (HCV) therapy has dramatically improved the possibility of cure for patients with genotype 1, but at the same time has increased the incidence of severe adverse events and the risk of reduced compliance. Here we present the case of a 72-year-old Caucasian male suffering from a genotype 1b HCV infection, with a previous history of virological breakthrough at the end of dual therapy with pegylated interferon and ribavirin at standard dosages. The patient was retreated with telaprevir-based triple therapy, and despite the early spontaneous interruption of treatment because of severe anemia and fatigue, he obtained a sustained virological response. This case suggests that in selected genotype 1 HCV-infected patients, primarily of subtype 1b, who require the interruption of anti-HCV therapy because of severe adverse events or reduced compliance, a successful treatment can be obtained even with a very short course of DAA-based triple therapy.
作为抗丙型肝炎病毒(HCV)治疗的基本组成部分,直接抗病毒药物(DAAs)的近期引入显著提高了1型基因型患者的治愈可能性,但同时也增加了严重不良事件的发生率以及依从性降低的风险。在此,我们报告一例72岁的白种男性病例,该患者患有1b型基因型HCV感染,既往在接受标准剂量聚乙二醇干扰素和利巴韦林联合治疗结束时曾出现病毒学突破。该患者接受了基于特拉匹韦的三联疗法再次治疗,尽管由于严重贫血和疲劳导致治疗早期自行中断,但他仍获得了持续病毒学应答。该病例表明,在因严重不良事件或依从性降低而需要中断抗HCV治疗的特定1型基因型HCV感染患者中,主要为1b亚型,即使采用基于DAA的三联疗法进行非常短疗程的治疗,也可获得成功治疗。