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聚乙二醇干扰素α-2a 联合利巴韦林治疗慢性丙型肝炎基因型 4 的安全性和疗效。

Safety and efficacy of treatment with pegylated interferon alpha-2a with ribavirin in chronic hepatitis C genotype 4.

机构信息

Consorcio Hospital General Universitario de Valencia, Spain.

出版信息

Ann Hepatol. 2013 Jan-Feb;12(1):30-5.

Abstract

The hepatitis C virus (HCV) genotype is an important predictive outcome parameter for pegylated interferon plus ribavirin therapy. Most published therapeutic trials to date have enrolled mainly patients with HCV genotypes 1, 2 and 3. Limited studies have focused on genotype 4 patients, who have had a poor representation in pivotal trials. Our aim was to evaluate the efficacy and safety of treatment with standard dose pegylated interferon alfa-2a in combination with weight-based ribavirin in patients with chronic hepatitis C genotype 4. In this prospective observational study, 198 patients with HCV-4 were included in this study from February 2004 to August 2005,188 patients who received at least 1 dose of drugs were included in the ITT analysis and they were treated with pegylated interferon alfa-2a and ribavirin for 48 weeks. Baseline and demographic characteristics, response to treatment at weeks 12, 48 and 72, and the nature and frequency of adverse effects were analyzed. Virological response at week 12 was achieved in 144 patients (76.6%). Virological response at the end of treatment was present in 110 patients (58.5%). At week 72, 99 patients presented SVR (52.7%). The reported adverse events were similar to those found in the literature for treatments of similar dose and duration. In conclusion, combined treatment with pegylated interferon alfa-2a and ribavirin was well tolerated and effective in chronic hepatitis C genotype 4, yielding response rates between those reported for genotype 1 and those of genotypes 2-3.

摘要

丙型肝炎病毒 (HCV) 基因型是聚乙二醇干扰素联合利巴韦林治疗的重要预测结果参数。迄今为止,大多数已发表的治疗试验主要招募了 HCV 基因型 1、2 和 3 的患者。有限的研究集中在基因型 4 患者,他们在关键试验中的代表性较差。我们的目的是评估标准剂量聚乙二醇干扰素 alfa-2a 联合利巴韦林治疗慢性丙型肝炎基因型 4 患者的疗效和安全性。在这项前瞻性观察性研究中,我们纳入了 2004 年 2 月至 2005 年 8 月期间的 198 例 HCV-4 患者,188 例接受至少 1 剂药物的患者纳入意向治疗分析,他们接受聚乙二醇干扰素 alfa-2a 和利巴韦林治疗 48 周。分析了基线和人口统计学特征、治疗 12、48 和 72 周时的反应以及不良事件的性质和频率。144 例患者(76.6%)在第 12 周实现了病毒学应答。110 例患者(58.5%)在治疗结束时实现了病毒学应答。在第 72 周时,99 例患者出现 SVR(52.7%)。报告的不良事件与文献中类似剂量和持续时间的治疗中发现的不良事件相似。总之,聚乙二醇干扰素 alfa-2a 和利巴韦林联合治疗在慢性丙型肝炎基因型 4 中耐受性良好且有效,其应答率介于基因型 1 和基因型 2-3 之间。

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