Queen Marys University of London, The Liver Unit, Blizard Institute, United Kingdom.
Bradford Teaching Hospitals Foundation Trust, Bradford, United Kingdom.
J Hepatol. 2014 Apr;60(4):699-705. doi: 10.1016/j.jhep.2013.11.011. Epub 2013 Nov 26.
BACKGROUND & AIMS: Patients with genotype 3 hepatitis C virus (HCV) infection and cirrhosis have poor response rates after 24 weeks treatment with pegylated interferon and ribavirin. Treatment for 48 weeks is therefore recommended, although the benefits of this are untested. We examined extended therapy in patients with genotype 3 HCV and advanced fibrosis.
Multicentre, open labelled randomized trial comparing therapy with 24 weeks pegylated interferon and ribavirin to 48 weeks of the same therapy.
136 patients completed the study. 67 received 24 weeks therapy and the SVR rate (48%) did not differ from that seen in the 69 patients who received 48 weeks therapy (42%). The response rates in patients with biopsy proven cirrhosis (13 patients treated for 24 weeks, 18 patients treated for 48 weeks) or cirrhosis proven on imaging (28 patients treated for 24 weeks and 25 patients treated for 48 weeks) were 46% in those treated for 24 weeks and 40% in those treated for 48 weeks. The differences were not significantly different. Treatment failure was due to relapse in the majority of patients.
Patients with genotype 3 HCV and advanced fibrosis do not benefit from extended therapy with pegylated interferon and ribavirin.
基因型 3 丙型肝炎病毒(HCV)感染和肝硬化患者接受聚乙二醇干扰素和利巴韦林治疗 24 周后应答率较差。因此建议进行 48 周治疗,尽管尚未验证其益处。我们研究了基因型 3 HCV 和晚期纤维化患者的延长治疗。
多中心、开放标签随机试验,比较 24 周聚乙二醇干扰素和利巴韦林治疗与相同治疗 48 周的疗效。
136 例患者完成了研究。67 例接受 24 周治疗,SVR 率(48%)与接受 48 周治疗的 69 例患者(42%)相似。肝活检证实肝硬化患者(24 周治疗 13 例,48 周治疗 18 例)或影像学证实肝硬化患者(24 周治疗 28 例,48 周治疗 25 例)的应答率分别为 46%和 40%。差异无统计学意义。治疗失败主要是由于复发。
基因型 3 HCV 和晚期纤维化患者不能从聚乙二醇干扰素和利巴韦林的延长治疗中获益。