Sustained virological response after ten days of triple anti-hepatitis C virus (HCV) therapy with telaprevir plus pegylated interferon and ribavirin in an HIV/HCV co-infected cirrhotic woman

被引:3
|
作者
Hasson, Hamid [1 ]
Messina, Emanuela [1 ,2 ]
Merli, Marco [1 ,2 ]
Della Torre, Liviana [1 ]
Morsica, Giulia [1 ]
Bagaglio, Sabrina [1 ]
Lazzarin, Adriano [1 ,2 ]
Uberti-Foppa, Caterina [1 ]
机构
[1] IRCCS Osped San Raffaele, Dept Infect Dis, I-20127 Milan, Italy
[2] Univ Vita Salute San Raffaele, Milan, Italy
关键词
Telaprevir; HIV/HCV co-infection; Liver cirrhosis; HIV;
D O I
10.1016/j.ijid.2014.08.011
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
The introduction of first-generation protease inhibitors for the treatment of chronic hepatitis C in subjects infected with hepatitis C virus (HCV) genotype 1 has significantly improved the sustained virological response (SVR) rate. As liver cirrhosis reduces the probability of achieving SVR, current guidelines discourage response-guided therapy in cirrhotic patients. We report the first case of a cirrhotic woman with chronic HCV and HIV co-infection achieving virological response after an ultra-short course of therapy. A 40-year-old HIV/HCV co-infected woman with compensated liver cirrhosis was treated with anti-HCV triple therapy containing telaprevir plus pegylated interferon and ribavirin. Baseline plasma HCV RNA was 3.6 log IU/ml and transaminases were within the normal range. She harboured IL28B rs12979860 C/C alleles. Ten days after starting therapy, the patient stopped treatment because of mild anorexia and nausea. Virological response was detected at treatment discontinuation and was maintained up to 24 weeks. This case describes an unexpected SVR after a 10-day course of antiviral therapy in a cirrhotic HIV/HCV co-infected woman presenting positive predictive factors for a response (low viral load, IL28B genotype). Nonetheless, there is no evidence to suggest a shorter duration of treatment in this subset of patients. (C) 2014 The Authors. Published by Elsevier Ltd on behalf of International Society for Infectious Diseases.
引用
收藏
页码:100 / 102
页数:3
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