Background: Pegylated interferon (PEG-IFN) plus ribavirin therapy is still recommended for elderly and/or cirrhotic patients. This study examined whether sustained virological response (SVR) to low-dose PEG-IFN-alpha 2a plus ribavirin therapy for elderly and/or cirrhotic patients could be predicted based on viral reduction within 2 weeks after therapy initiation or interleukin IL-(28B) polymorphism and viral mutations. Methods: Participants comprised 115 elderly (>= 65 years) and/or cirrhotic patients with genotype-1b and high viral load. Reduced doses of PEG-IFN-alpha 2a (90 mu g/kg/week) and ribavirin (400-800 mu g/day) were administered for 48-72 weeks based on virological response of each patient. Results: SVR was achieved in 34% (39/115), and treatment was discontinued in 15% (17/115). Univariate analysis identified age, alpha-fetoprotein, fibrosis marker, interferon sensitivity-determining region (ISDR), IL-28B polymorphism and level of viral reduction within 2 weeks as factors contributing significantly to SVR. However, no significant differences were noted in core amino acid substitutions. Multivariate analysis identified age, hyaluronic acid, ISDR and viral reduction as factors independently associated with SVR. Positive predictive value (PPV) and negative predictive value (NPV) of SVR based on the level of viral reduction at 2 weeks (cutoff level, 1.7 log IU/ml) were 83% and 84%, respectively. The PPV of SVR based on IL-28B major and ISDR mutant was 70%, and the NPV of SVR based on IL-28B minor and wild-type ISDR was 89%. Conclusions: Evaluations of viral reduction at 2 weeks or both IL-28B and ISDR are useful to predict SVR to lowdose PEG-IFN-alpha 2a plus ribavirin therapy for elderly and/or cirrhotic patients.
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Kobe Asahi Hosp, Dept Gastroenterol, Nagata Ku, Kobe, Hyogo 6530801, JapanKobe Asahi Hosp, Dept Gastroenterol, Nagata Ku, Kobe, Hyogo 6530801, Japan
Kim, Soo Ryang
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El-Shamy, Ahmed
Imoto, Susumu
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Kobe Asahi Hosp, Dept Gastroenterol, Nagata Ku, Kobe, Hyogo 6530801, JapanKobe Asahi Hosp, Dept Gastroenterol, Nagata Ku, Kobe, Hyogo 6530801, Japan
Imoto, Susumu
Kim, Ke Ih
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Kobe Asahi Hosp, Dept Gastroenterol, Nagata Ku, Kobe, Hyogo 6530801, JapanKobe Asahi Hosp, Dept Gastroenterol, Nagata Ku, Kobe, Hyogo 6530801, Japan
Kim, Ke Ih
Ide, Yoshi-hiro
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Kobe Univ, Grad Sch Med, Div Microbiol, Ctr Infect Dis, Kobe, Hyogo 657, JapanKobe Asahi Hosp, Dept Gastroenterol, Nagata Ku, Kobe, Hyogo 6530801, Japan
Ide, Yoshi-hiro
Deng, Lin
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Kobe Univ, Grad Sch Med, Div Microbiol, Ctr Infect Dis, Kobe, Hyogo 657, JapanKobe Asahi Hosp, Dept Gastroenterol, Nagata Ku, Kobe, Hyogo 6530801, Japan
Deng, Lin
Shoji, Ikuo
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Kobe Univ, Grad Sch Med, Div Microbiol, Ctr Infect Dis, Kobe, Hyogo 657, JapanKobe Asahi Hosp, Dept Gastroenterol, Nagata Ku, Kobe, Hyogo 6530801, Japan
Shoji, Ikuo
Tanaka, Yasuhito
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Nagoya City Univ, Grad Sch Med Sci, Dept Virol, Nagoya, Aichi, Japan
Nagoya City Univ, Grad Sch Med Sci, Liver Unit, Nagoya, Aichi, JapanKobe Asahi Hosp, Dept Gastroenterol, Nagata Ku, Kobe, Hyogo 6530801, Japan