Di Bisceglie A M, Ghalib R H, Hamzeh F M, Rustgi V K
Division of Gastroenterology and Hepatology, Saint Louis University School of Medicine, St Louis, MO 63110, USA.
J Viral Hepat. 2007 Oct;14(10):721-9. doi: 10.1111/j.1365-2893.2007.00862.x.
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.
感染丙型肝炎病毒(HCV)1型且血清HCV RNA浓度超过800 000 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,比较它们的初步研究得出了不同的结果。我们比较了380例感染HCV 1型且病毒载量高的患者接受聚乙二醇化干扰素α-2a加利巴韦林与聚乙二醇化干扰素α-2b加利巴韦林治疗12周后的病毒学应答情况。我们观察到随着时间推移两组在病毒载量降低方面无差异,在接受聚乙二醇化干扰素α-2a或聚乙二醇化干扰素α-2b加利巴韦林治疗并实现早期病毒学应答(EVR,定义为HCV RNA浓度降低≥2个对数或在12周时HCV RNA检测不到)的患者百分比方面也无差异(分别为66%和63%)。与接受聚乙二醇化干扰素α-2a加利巴韦林治疗的患者(1%-2%)相比,接受聚乙二醇化干扰素α-2b加利巴韦林治疗的患者血清干扰素水平更频繁地低于定量水平(58%-68%)。接受聚乙二醇化干扰素α-2b加利巴韦林治疗的患者因安全原因停药的比例更高(6%对1%)。总之,相当一部分感染HCV 1型且病毒载量高的患者在接受聚乙二醇化干扰素和利巴韦林治疗时可实现EVR。在与相同剂量的利巴韦林(1000-1200 mg/天)联合使用时,两种聚乙二醇化干扰素在治疗的前12周显示出相当的抗HCV活性,但接受聚乙二醇化干扰素α-2b加利巴韦林治疗的患者因安全原因停药的情况更多。