Di Bisceglie Adrian M, Hoofnagle Jay H
Division of Gastroenterology and Hepatology and the Department of Internal Medicine, Saint Louis University School of Medicine, Saint Louis University, St. Louis, MO 63110, USA.
Hepatology. 2002 Nov;36(5 Suppl 1):S121-7. doi: 10.1053/jhep.2002.36228.
The highest response rates to antiviral therapy for the treatment of chronic hepatitis C have been achieved using the combination of peginterferon and ribavirin. Recently completed controlled trials have reported rates of sustained virological response (SVR) between 50% and 60% in patients treated with higher doses of peginterferon and ribavirin, which was 5% to 10% higher with standard doses of interferon alfa and ribavirin. The major determinant of outcome of therapy is hepatitis C virus (HCV) genotype. With the combination of peginterferon and ribavirin, patients with genotype 1 achieve response rates of 40% to 45%, compared with rates approaching 80% with genotypes 2 or 3. Importantly, patients with HCV genotype 1 achieve higher rates of response with 48 weeks than with 24 weeks of therapy, whereas patients with genotypes 2 and 3 are adequately treated with a 24-week course. Furthermore, patients with genotypes 2 and 3 require only 800 mg of ribavirin daily to achieve optimal response rates, whereas 1,000 to 1,200 mg daily is needed for patients with genotype 1. Future studies should focus on optimizing the dose of peginterferon and ribavirin by patient characteristics, particularly on resolving the issue of weight-based dosing. For patients with good prognostic factors, a lower dose and shorter course of peginterferon may be adequate for full effect. Importantly, research is needed to show how treatment regimens can best be applied to other patient groups with hepatitis C, such as patients with acute hepatitis, human immunodeficiency virus coinfection, renal disease, solid-organ transplant, neuropyschiatric disease, autoimmunity, and alcohol or substance abuse.
聚乙二醇干扰素与利巴韦林联合使用时,在治疗慢性丙型肝炎方面取得了对抗病毒治疗的最高应答率。最近完成的对照试验报告称,接受高剂量聚乙二醇干扰素和利巴韦林治疗的患者持续病毒学应答(SVR)率在50%至60%之间,这比使用标准剂量的α干扰素和利巴韦林时高出5%至10%。治疗结果的主要决定因素是丙型肝炎病毒(HCV)基因型。使用聚乙二醇干扰素和利巴韦林联合治疗时,基因型1的患者应答率为40%至45%,而基因型2或3的患者应答率接近80%。重要的是,基因型1的HCV患者接受48周治疗的应答率高于24周治疗,而基因型2和3的患者接受24周疗程即可得到充分治疗。此外,基因型2和3的患者每天仅需800毫克利巴韦林就能达到最佳应答率,而基因型1的患者每天需要1000至1200毫克。未来的研究应侧重于根据患者特征优化聚乙二醇干扰素和利巴韦林的剂量,特别是解决基于体重给药的问题。对于预后因素良好的患者,较低剂量和较短疗程的聚乙二醇干扰素可能足以产生充分疗效。重要的是,需要开展研究以表明治疗方案如何能最佳地应用于其他丙型肝炎患者群体,如急性肝炎患者、合并人类免疫缺陷病毒感染的患者、肾病患者、实体器官移植患者、神经精神疾病患者、自身免疫性疾病患者以及酗酒或药物滥用患者。