Department of Gastroenterology and Hepatology, Victor Babes University of Medicine and Pharmacy, Timisoara, Romania.
J Gastrointestin Liver Dis. 2011 Sep;20(3):293-8.
Patients with HCV liver cirrhosis are a category difficult to treat. The aim of this study was to establish the sustained virological response (SVR) rates in HCV patients with liver cirrhosis treated with standard of care therapy (Pegylated Interferon and Ribavirin for 48 weeks in genotypes 1 and 4 and 24 weeks in genotypes 2 and 3).
Searching the PubMed, Medline, Lilacs, Scopus, Ovid and Medscape databases we identified all the articles published until February 2011 that included only HCV cirrhotic patients. These studies evaluated the SVR after standard of care treatment: Pegylated Interferon alpha 2a (doses ranging between 135-180 µg/week) or Pegylated Interferon alpha 2b (1 or 1.5 µg/kg/week) and Ribavirin (doses ranging between 800-1200 mg/day). We used the following key words: HCV, liver cirrhosis, sustained virological response (SVR).
The overall SVR rate was 33.3% (95%CI-confidence interval=30.6-36.2%). SVR was significantly higher in patients with genotypes 2 and 3 (422 patients) as compared to those with genotypes 1 and 4 (692 patients): 55.4% (95%CI=50.7-60.1) versus 21.7% (95%CI=18.7-25), p < 0.0001.
The overall SVR rate in cirrhotic patients treated with standard of care therapy is 33.3%, but lower in cases affected by genotypes 1 and 4 (21.6%) which makes them a priority regarding the development of more potent drugs for effective treatment.
丙型肝炎肝硬化患者是一类难以治疗的人群。本研究旨在确定采用标准治疗方案(基因型 1 和 4 患者使用聚乙二醇干扰素和利巴韦林治疗 48 周,基因型 2 和 3 患者使用 24 周)治疗的丙型肝炎肝硬化患者的持续病毒学应答(SVR)率。
我们检索了 PubMed、Medline、Lilacs、Scopus、Ovid 和 Medscape 数据库,检索截至 2011 年 2 月发表的所有仅纳入丙型肝炎肝硬化患者的文章。这些研究评估了标准治疗后(聚乙二醇干扰素α 2a 剂量范围为 135-180μg/周或聚乙二醇干扰素α 2b 剂量为 1 或 1.5μg/kg/周,联合利巴韦林剂量范围为 800-1200mg/天)的 SVR。我们使用了以下关键词:HCV、肝硬化、持续病毒学应答(SVR)。
总体 SVR 率为 33.3%(95%CI 置信区间为 30.6-36.2%)。基因型 2 和 3(422 例)患者的 SVR 显著高于基因型 1 和 4(692 例)患者:55.4%(95%CI=50.7-60.1)比 21.7%(95%CI=18.7-25),p<0.0001。
采用标准治疗方案治疗的肝硬化患者的总体 SVR 率为 33.3%,但基因型 1 和 4 患者的 SVR 率较低(21.6%),因此对于开发更有效的治疗药物具有优先权。