Scotto Gaetano, Fazio Vincenzina, Palumbo Emilio, Cibelli Donatella Concetta, Saracino Annalisa, Angarano Gioacchino
Clinic of Infectious Diseases, University of Foggia, Italy.
New Microbiol. 2005 Jan;28(1):23-9.
This prospective open-label randomized trial of chronic hepatitis C genotype-1b patients compared compared the efficacy and safety of peg-interferon alfa-2b administered once-weekly versus interferon alfa-2b thrice-weekly or daily, both in combination with ribavirin. Seventy-eight previously untreated patients, with biopsy-documented genotype 1 chronic HCV and persistently elevated ALT levels and detectable HCV RNA, were randomized (26 subjects each) to receive: interferon alfa-2b at 6MIUs.c./three-times-weekly (group A) or interferon alfa-2b, 3MIUs.c./daily (group B) or peg-interferon alfa-2b 1.5mcg/Kg s.c./once-weekly (group C). All regimens included standard weight-based doses of ribavirin (800, 1,000 or 1,200 mg/day) administered for 52-weeks. Patients in the three groups were comparable for age, sex, viral load, ALT value and histological-activity-index (HAI). Therapy was completed by 22, 20 and 23 patients in groups A, B and C, respectively. At the end of treatment, a complete (biochemical and virological) response was observed in 50.0% patients of group A, 57.7% of group B and 65.4% of group C. After an additional 24-weeks of follow-up, a sustained response was observed in 26.9%, 46.1% and 50.0% of patients in groups A, B or C, respectively. Therapy was discontinued by 4, 6 and 2 patients because of adverse events in the above three groups. In naive patients with chronic genotype-lb hepatitis C, a 48 week therapy with peg-interferon or interferon at daily doses combined with ribavirin were both more effective than treatment with thrice-weekly interferon in inducing end of treatment and sustained response. Peg-interferon treatment was better tolerated and provoked significantly fewer therapy discontinuations.
这项针对慢性丙型肝炎基因1b型患者的前瞻性开放标签随机试验,比较了聚乙二醇干扰素α-2b每周一次与干扰素α-2b每周三次或每日一次联合利巴韦林给药的疗效和安全性。78例既往未接受治疗的患者,经活检证实为基因1型慢性丙型肝炎,谷丙转氨酶(ALT)水平持续升高且可检测到丙型肝炎病毒核糖核酸(HCV RNA),被随机分组(每组26例)接受:6百万国际单位(MIUs)/平方厘米的干扰素α-2b,每周三次(A组);或3MIUs/平方厘米的干扰素α-2b,每日一次(B组);或1.5微克/千克皮下注射的聚乙二醇干扰素α-2b,每周一次(C组)。所有治疗方案均包括根据体重给予标准剂量的利巴韦林(800、1000或1200毫克/天),持续给药52周。三组患者在年龄、性别、病毒载量、ALT值和组织学活性指数(HAI)方面具有可比性。A、B、C组分别有22、20和23例患者完成治疗。治疗结束时,A组、B组和C组分别有50.0%、57.7%和65.4%的患者出现完全(生化和病毒学)应答。在额外随访24周后,A组、B组和C组分别有26.9%、46.1%和50.0%的患者出现持续应答。上述三组分别有4例、6例和2例患者因不良事件而停药。在初治的慢性基因1b型丙型肝炎患者中,聚乙二醇干扰素或每日剂量的干扰素联合利巴韦林进行48周治疗,在诱导治疗结束时的应答和持续应答方面均比每周三次的干扰素治疗更有效。聚乙二醇干扰素治疗耐受性更好,导致停药的情况明显更少。