Durability of SVR in chronic hepatitis C patients treated with peginterferon- alpha 2a/ribavirin in combination with a direct-acting anti-viral

The introduction of direct-acting anti-virals has increased sustained virological response (SVR) rates in chronic hepatitis C genotype 1 infection. At present, data on long-term durability of viral eradication after successful triple therapy are lacking. To evaluate the long-term durability of viral...

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Veröffentlicht in:Alimentary pharmacology & therapeutics 2013-07, Vol.38 (2), p.118-123
Hauptverfasser: Rutter, K, Hofer, H, Beinhardt, S, Dulic, M, Gschwantler, M, Maieron, A, Laferl, H, Staettermayer, A F, Scherzer, T-M, Strassl, R, Holzmann, H, Steindl-Munda, P, Ferenci, P
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container_end_page 123
container_issue 2
container_start_page 118
container_title Alimentary pharmacology & therapeutics
container_volume 38
creator Rutter, K
Hofer, H
Beinhardt, S
Dulic, M
Gschwantler, M
Maieron, A
Laferl, H
Staettermayer, A F
Scherzer, T-M
Strassl, R
Holzmann, H
Steindl-Munda, P
Ferenci, P
description The introduction of direct-acting anti-virals has increased sustained virological response (SVR) rates in chronic hepatitis C genotype 1 infection. At present, data on long-term durability of viral eradication after successful triple therapy are lacking. To evaluate the long-term durability of viral eradication in patients treated with triple therapy, including direct-acting anti-virals. Patients who participated in randomised, controlled trials or an extended access programme of treatment with peginterferon- alpha 2a/ribavirin in combination with a direct-acting anti-viral (telaprevir, danoprevir, faldaprevir, simeprevir, mericitabine, balapiravir) were followed after achieving SVR. The median follow-up after the patients was 21 (range: 7-64) months. One hundred and three patients with chronic hepatitis C genotype 1 infection [f/m: 34/69; GT-1b: 67 GT-1a: 34, GT-4: 2; mean age: 47.6 years (45.5-49.7; 95% CI)] achieving a SVR triple therapy were followed. Two cases of late relapses (2/103, 1.9%; 95% CI: 0.24-6.8) were observed. One patient was cirrhotic, both carried the genotype 1b and completed the prescribed treatment. The relapses occurred 8 and 12 months after cessation of anti-viral treatment. Cloning sequencing revealed identical sequence in both patients. Resistance analysis revealed no presence of viral resistance. Like the SVR after peginterferon- alpha 2/ribavirin combination treatment, HCV eradication after triple therapy remains durable after long-term follow-up.
doi_str_mv 10.1111/apt.12350
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At present, data on long-term durability of viral eradication after successful triple therapy are lacking. To evaluate the long-term durability of viral eradication in patients treated with triple therapy, including direct-acting anti-virals. Patients who participated in randomised, controlled trials or an extended access programme of treatment with peginterferon- alpha 2a/ribavirin in combination with a direct-acting anti-viral (telaprevir, danoprevir, faldaprevir, simeprevir, mericitabine, balapiravir) were followed after achieving SVR. The median follow-up after the patients was 21 (range: 7-64) months. One hundred and three patients with chronic hepatitis C genotype 1 infection [f/m: 34/69; GT-1b: 67 GT-1a: 34, GT-4: 2; mean age: 47.6 years (45.5-49.7; 95% CI)] achieving a SVR triple therapy were followed. Two cases of late relapses (2/103, 1.9%; 95% CI: 0.24-6.8) were observed. One patient was cirrhotic, both carried the genotype 1b and completed the prescribed treatment. 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The relapses occurred 8 and 12 months after cessation of anti-viral treatment. Cloning sequencing revealed identical sequence in both patients. Resistance analysis revealed no presence of viral resistance. Like the SVR after peginterferon- alpha 2/ribavirin combination treatment, HCV eradication after triple therapy remains durable after long-term follow-up.</abstract><doi>10.1111/apt.12350</doi></addata></record>
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subjects Hepatitis C virus
title Durability of SVR in chronic hepatitis C patients treated with peginterferon- alpha 2a/ribavirin in combination with a direct-acting anti-viral
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