首页> 外文期刊>Journal of viral hepatitis. >Early virologic response after peginterferon alpha-2a plus ribavirin or peginterferon alpha-2b plus ribavirin treatment in patients with chronic hepatitis C.
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Early virologic response after peginterferon alpha-2a plus ribavirin or peginterferon alpha-2b plus ribavirin treatment in patients with chronic hepatitis C.

机译:慢性丙型肝炎患者接受聚乙二醇干扰素α-2a加利巴韦林或聚乙二醇干扰素α-2b加利巴韦林治疗后的早期病毒学应答。

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Patients infected with hepatitis C virus (HCV) genotype 1 and with serum HCV RNA concentrations over 800 000 IU/mL have relatively low rates of virologic response to pegylated interferons. The 2 forms of pegylated interferon have different pharmacokinetic profiles, and pilot studies comparing them have yielded varying results. We compared the virologic response to 12 weeks of treatment with peginterferon alpha-2a plus ribavirin vs peginterferon alpha-2b plus ribavirin in 380 patients who were infected with HCV genotype 1 and had high viral loads. We observed no between-group differences in viral load reduction over time and no differences in the percentage of patients treated with peginterferon alpha-2a or peginterferon alpha-2b plus ribavirin who achieved early virologic response (EVR), defined as >/=2-log reduction in HCV RNA concentration or undetectable HCV RNA at 12 weeks (66%vs 63%). Serum levels of interferon were more frequently below the level of quantitation in patients treated with peginterferon alpha-2b plus ribavirin (58-68%) than in those treated with peginterferon alpha-2a plus ribavirin (1-2%). Patients treated with peginterferon alpha-2b plus ribavirin had higher rates of discontinuation for safety reasons (6%vs 1%). In conclusion, a substantial percentage of patients infected with HCV genotype 1 and high viral load can achieve EVR when treated with peginterferon and ribavirin. The 2 pegylated interferons showed comparable anti-HCV activity during the first 12 weeks of treatment when combined with the same doses of ribavirin (1000-1200 mg/day), but discontinuations for safety reasons were higher in the patients treated with peginterferon alpha-2b plus ribavirin.
机译:感染了1型丙型肝炎病毒(HCV)且血清HCV RNA浓度超过80万IU / mL的患者对聚乙二醇化干扰素的病毒学应答率相对较低。两种形式的聚乙二醇化干扰素具有不同的药代动力学特征,比较它们的先导研究得出不同的结果。我们比较了380例感染HCV基因型1且病毒载量高的患者中,peginterferonα-2a加利巴韦林与peginterferonα-2b加利巴韦林治疗12周的病毒学应答。我们没有观察到随时间推移病毒载量减少的组间差异,也没有发现接受聚乙二醇干扰素α-2a或聚乙二醇干扰素α-2b加利巴韦林治疗的患者达到早期病毒学应答(EVR)(定义为> / = 2-)的百分比差异在第12周时,HCV RNA浓度或未检测到的HCV RNA的对数降低(66%对63%)。与聚乙二醇干扰素α-2a加利巴韦林治疗的患者(1-2%)相比,聚乙二醇干扰素α-2b加利巴韦林治疗的患者的血清干扰素水平经常低于定量水平(58-68%)。出于安全原因,接受聚乙二醇干扰素α-2b加利巴韦林治疗的患者停用率较高(6%vs. 1%)。总之,当使用聚乙二醇干扰素和利巴韦林治疗时,相当大比例的HCV基因型1和高病毒载量感染患者可以实现EVR。当与相同剂量的利巴韦林(1000-1200 mg / day)联合使用时,两种聚乙二醇化干扰素在治疗的前12周内显示出可比的抗HCV活性,但是出于安全原因,接受聚乙二醇干扰素α-2b治疗的患者停用率更高加利巴韦林。

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