Durability of the response to peginterferon-α2b and ribavirin in patients with chronic hepatitis C: a cohort study in the routine clinical setting

OBJECTIVESTo evaluate whether, in chronic hepatitis C-positive naive patients recruited in the routine clinical setting and treated with pegylated-interferon-α2b (Peg-IFN) and ribavirin (RBV), the sustained virologic response (SVR) is durable over the long term and whether it is associated with a de...

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Veröffentlicht in:European journal of gastroenterology & hepatology 2014-01, Vol.26 (1), p.52-58
Hauptverfasser: Giordanino, Chiara, Sacco, Marco, Ceretto, Simone, Smedile, Antonina, Ciancio, Alessia, Cariti, Giuseppe, De Blasi, Tiziano, Picciotto, Antonio, Marenco, Simona, Grasso, Alessandro, Pirisi, Mario, Smirne, Carlo, Colletta, Cosimo, Traverso, Antonio, Mazzucco, Dario, Ciccone, Giovannino, Simondi, Daniele, Rizzetto, Mario, Saracco, Giorgio
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Sprache:eng
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Zusammenfassung:OBJECTIVESTo evaluate whether, in chronic hepatitis C-positive naive patients recruited in the routine clinical setting and treated with pegylated-interferon-α2b (Peg-IFN) and ribavirin (RBV), the sustained virologic response (SVR) is durable over the long term and whether it is associated with a decrease in liver complications and incidence of glucose abnormalities. PATIENTS AND METHODSThis was a prospective long-term follow-up study of 182 naive patients enrolled in 2001–2002 and treated with Peg-IFN and RBV and followed up to December 2010, with clinical, biochemical, and virological evaluations every 6–12 months. RESULTSNone of the 115 (63.2%) sustained responders showed late viremic relapse during the follow-up. SVR was better defined at 24 weeks (16/16 relapsers, 100%) than at 12 weeks after the end of therapy (14/16 relapsers, 87.5%). On multivariable analysis, viral genotype (odds ratio 0.16, 95% confidence interval 0.07–0.36, P=0.0001) and a greater than 20% RBV reduction (odds ratio 5.21, 95% confidence interval 1.54–17.67, P=0.008) predicted long-term response (LTR) independently. The incidence of cirrhosis was significantly higher among nonresponders (21.3%) compared with long-term responders (0.9%, P≤0.0001), but the risk of developing glucose abnormalities was not significantly reduced in long-term responders (hazard ratio 1.36, P=0.363). Hepatocellular carcinoma occurred only in three cases. CONCLUSIONSVR achieved in patients treated in the routine clinical setting with Peg-IFN and RBV is durable over the long term and LTR significantly reduces the risk of progression to cirrhosis; however, in a population with mild liver fibrosis, the clinical impact of LTR on the risk of glucose abnormalities seems negligible.
ISSN:0954-691X
1473-5687
DOI:10.1097/MEG.0b013e328362dc99