Sustained virological response to antiviral therapy improves survival rate in patients with recurrent hepatitis C virus infection after liver transplantation

被引:13
|
作者
Kawaoka, Tomokazu [1 ]
Takahashi, Shoichi [1 ]
Kawakami, Yoshiiku [1 ]
Tsuge, Masataka [1 ]
Hiramatsu, Akira [1 ]
Imamura, Michio [1 ]
Hyogo, Hideyuki [1 ]
Aikata, Hiroshi [1 ]
Ishiyama, Kohei [2 ]
Tashiro, Hirotaka [2 ]
Ohdan, Hideki [2 ]
Tanaka, Junko [3 ]
Chayama, Kazuaki [1 ]
机构
[1] Hiroshima Univ, Grad Sch Biomed Sci, Dept Gastroenterol & Metab, Hiroshima 7348551, Japan
[2] Hiroshima Univ, Grad Sch Biomed Sci, Dept Surg, Div Frontier Med Sci,Programs Biomed Res, Hiroshima 7348551, Japan
[3] Hiroshima Univ, Dept Epidemiol Infect Dis Control & Prevent, Grad Sch Biomed Sci, Hiroshima 7348551, Japan
关键词
interferon therapy; HCV; LT; SVR; PLASMA-CELL HEPATITIS; LONG-TERM SURVIVAL; INTERFERON THERAPY; REDUCES INCIDENCE; TRIPLE THERAPY; GENOTYPE; 1B; RECIPIENTS; RIBAVIRIN; DACLATASVIR; TELAPREVIR;
D O I
10.1111/hepr.12447
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Aim: Previous European and North American studies analyzed the relationship between survival rate and sustained virological response (SVR) to interferon (IFN) therapy in patients with recurrent hepatitis C viral (HCV) infection after liver transplantation (LT). The present study was designed to define the same relationship in Japanese patients who had undergone LT. Methods: Forty-seven patients (genotype 1, 40; genotype 2, 7) with recurrent HCV after LT were treated with pegylated interferon (PEG IFN) or IFN/ribavirin (RBV). In possible, within 3 months after LT, patients started treatment with PEG IFN-alpha-2b or IFN-alpha-2b s.c. once weekly combined with RBV (200 mg/day). Results: The SVR rate was 51% (24/47) for all patients, 42.5% (17/40) for genotype 1 and 100% (7/7) for genotype 2. The median follow-up period was 71 months (range, 24-152). The survival rate of 24 patients who achieved SVR was 95% at 5 years and 92% at 10 years. These rates were significantly better than those of 23 patients who did not achieve SVR (82% at 5 years, 58% at 10 years) (P = 0.027). Two patients of the SVR group died during follow up (due to hepatocellular carcinoma in one and chronic rejection in one), while six non-SVR patients died during the same period (three died due to liver failure by recurrent HCV). Conclusion: SVR following IFN therapy contributes to improvement of survival rate in patients with recurrent post-LT HCV infection.
引用
收藏
页码:1047 / 1054
页数:8
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