A multicenter survey of re-treatment with pegylated interferon plus ribavirin combination therapy for patients with chronic hepatitis C in Japan

被引:14
|
作者
Oze, Tsugiko [1 ]
Hiramatsu, Naoki [1 ]
Mita, Eiji [3 ]
Akuta, Norio [4 ]
Sakamoto, Naoya [5 ]
Nagano, Hiroaki [2 ]
Itoh, Yoshito [7 ]
Kaneko, Shuichi [8 ]
Izumi, Namiki [6 ]
Nomura, Hideyuki [9 ]
Hayashi, Norio [10 ]
Takehara, Tetsuo [1 ]
机构
[1] Osaka Univ, Dept Gastroenterol & Hepatol, Grad Sch Med, Suita, Osaka 5650871, Japan
[2] Osaka Univ, Dept Surg, Grad Sch Med, Suita, Osaka 5650871, Japan
[3] Natl Hosp Org Osaka Natl Hosp, Osaka, Japan
[4] Toranomon Gen Hosp, Tokyo, Japan
[5] Tokyo Med & Dent Univ, Dept Gastroenterol & Hepatol, Tokyo, Japan
[6] Japanese Red Cross Musashino Hosp, Tokyo, Japan
[7] Kyoto Prefectural Univ Med, Grad Sch Med Sci, Kyoto, Japan
[8] Kanazawa Univ, Dept Gastroenterol, Kanazawa, Ishikawa, Japan
[9] Shin Kokura Hosp, Kitakyushu, Fukuoka, Japan
[10] Kansai Rosai Hosp, Amagasaki, Hyogo, Japan
关键词
chronic hepatitis C; pegylated interferon and ribavirin combination therapy; re-treatment; GENOTYPE; 1; TREATMENT DURATION; PEGINTERFERON; HCV; TELAPREVIR; RELAPSE; IL28B; ALPHA;
D O I
10.1111/j.1872-034X.2012.01056.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Aim: This study aimed to clarify the factors associated the efficacy of re-treatment with pegylated interferon (PEG IFN) plus ribavirin combination therapy for patients with chronic hepatitis C who had failed to respond to previous treatment. Methods: One hundred and forty-three patients who had previously shown relapse (n = 79), non-response (n = 34) or intolerance (n = 30) to PEG IFN plus ribavirin were re-treated with PEG IFN plus ribavirin. Results: Twenty-five patients with intolerance to previous treatment completed re-treatment and the sustained virological response (SVR) rates were 55% and 80% for hepatitis C virus (HCV) genotype 1 and 2, respectively. On re-treatment of the 113 patients who completed the previous treatment, the SVR rates were 48% and 63% for genotype 1 and 2, respectively. Relapse after previous treatment and a low baseline HCV RNA level on re-treatment were associated with SVR in genotype 1 (P < 0.001). Patients with the interleukin-28B major genotype responded significantly better and earlier to re-treatment, but the difference in the SVR rate did not reach a significant level between the major and minor genotypes (P = 0.09). Extended treatment of 72 weeks raised the SVR rate among the patients who attained complete early virological response but not rapid virological response with re-treatment (72 weeks, 73%, 16/22, vs 48 weeks, 38%, 5/13, P < 0.05). Conclusion: Relapse after previous treatment and a low baseline HCV RNA level have predictive values for a favorable response of PEG IFN plus ribavirin re-treatment for HCV genotype 1 patients. Re-treatment for 72 weeks may lead to clinical improvement for genotype 1 patients with complete early virological response and without rapid virological response on re-treatment.
引用
收藏
页码:35 / 43
页数:9
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