کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
3371094 1219105 2007 7 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Efficacy and safety of peg-IFN alfa-2a with ribavirin for the treatment of HCV/HIV coinfected patients who failed previous IFN based therapy
موضوعات مرتبط
علوم زیستی و بیوفناوری ایمنی شناسی و میکروب شناسی میکروبیولوژی و بیوتکنولوژی کاربردی
پیش نمایش صفحه اول مقاله
Efficacy and safety of peg-IFN alfa-2a with ribavirin for the treatment of HCV/HIV coinfected patients who failed previous IFN based therapy
چکیده انگلیسی

BackgroundInterferon (IFN) regimens for HCV treatment are less effective in HCV/HIV-coinfected patients. There are no effective treatments for patients who fail IFN therapies. We examined the safety and efficacy of peginterferon alfa-2a (peg-IFNα-2a) plus ribavirin (RBV) in 41 HCV/HIV-coinfected patients non-responsive to prior IFN treatment.MethodsPatients received peg-IFNα-2a (180 mg/week) plus RBV (800 mg/day) for 24 weeks (n = 41). At week 24, patients with non-detectable HCV RNA or ≥2-log decrease from baseline, received peg-IFNα-2a (180 mg/week) plus RBV (800 mg/day) for 24 weeks further. Patients not responding to treatment at week 24 were discontinued.ResultsIntent to treat (ITT) sustained viral response (SVR) was 21.9%. Patients who received at least 24 weeks of peg-IFNα-2a plus RBV treatment (n = 35), SVR rates were 25.7%. SVR was associated with significant improvements in liver histology grade (p = 0.02), stage (p = 0.02), and fibrosis progression rate (FPR) (p = 0.03). Patients that failed to achieve SVR had statistically significant decreases in grade (p = 0.09) and FPR (p = 0.01).Conclusionpeg-IFNα-2a plus RBV is effective and safe to achieve SVR in HCV/HIV coinfected patients non-responsive to prior IFN treatment. Patients that achieve SVR have significant improvements in liver histology parameters. In patients that do not achieve SVR there are histological benefits beyond virological response that suggest that peg-IFNα-2a + RBV therapy may decrease risk of progression to end stage liver disease.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Journal of Clinical Virology - Volume 38, Issue 1, January 2007, Pages 32–38
نویسندگان
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