Enríquez J, Gallego A, Torras X, Pérez-Olmeda T, Diago M, Soriano V, Luján M S, García-Samaniego J
Department of Gastroenterology, Hospital de la Sta Creu i St Pau, Barcelona, Spain.
J Viral Hepat. 2000 Nov;7(6):403-8. doi: 10.1046/j.1365-2893.2000.00243.x.
We assessed the efficacy of interferon (IFN) plus ribavirin over 24 or 48 weeks for the retreatment of patients with chronic hepatitis C who had relapsed or did not respond to a previous course of IFN. One-hundred and twenty patients (69 non-responders and 51 relapsers) were randomly assigned to receive IFN-alpha2b (3 million units thrice weekly) plus ribavirin (1,000-1,200 mg per day) for 24 weeks (group A: 58 patients) or 48 weeks (group B: 62 patients). Treatment was discontinued at week 12 if the alanine aminotransferase (ALT) level remained elevated. The rate of sustained response was 15.5% in group A and 37.1% in group B (P = 0.013). Relapsers treated for 48 weeks had a sustained response rate of 66.6% compared with a sustained response rate of only 25% in those treated for 24 weeks (P = 0.004). Moreover, a sustained response was seen in 14.3% of non-responders treated for 48 weeks and in 8.8% of those treated for 24 weeks (P = 0.71). Fifty-three per cent of patients with a normal ALT level and undetectable hepatitis C virus (HCV) RNA at week 12 had a sustained response compared with 14% of those who were HCV RNA positive at week 12 (P < 0.001). Independent predictive factors of sustained response were: therapy for 48 weeks (P = 0.0026), relapse after IFN treatment (P = 0.0006), loss of HCV RNA at week 12 (P = 0.0008) and HCV genotype non-1 (P = 0.024). Hence, in patients with chronic hepatitis C who failed to respond to a previous course of IFN monotherapy, combination therapy with IFN plus ribavirin for 48 weeks seems to be more effective than IFN plus ribavirin for 24 weeks.
我们评估了干扰素(IFN)联合利巴韦林治疗24周或48周对既往使用IFN治疗复发或无反应的慢性丙型肝炎患者再次治疗的疗效。120例患者(69例无反应者和51例复发者)被随机分配接受α-2b干扰素(300万单位,每周3次)联合利巴韦林(每日1000 - 1200mg)治疗24周(A组:58例患者)或48周(B组:62例患者)。如果丙氨酸氨基转移酶(ALT)水平持续升高,则在第12周停止治疗。A组的持续应答率为15.5%,B组为37.1%(P = 0.013)。接受48周治疗的复发者持续应答率为66.6%,而接受24周治疗者的持续应答率仅为25%(P = 0.004)。此外,接受48周治疗的无反应者中14.3%出现持续应答,接受24周治疗者中这一比例为8.8%(P = 0.71)。第12周ALT水平正常且丙型肝炎病毒(HCV)RNA检测不到的患者中53%出现持续应答,而第12周HCV RNA阳性的患者中这一比例为14%(P < 0.001)。持续应答的独立预测因素为:治疗48周(P = 0.0026)、IFN治疗后复发(P = 0.0006)、第12周HCV RNA转阴(P = 0.0008)和HCV非1型基因型(P = 0.024)。因此,对于既往IFN单药治疗无效的慢性丙型肝炎患者,IFN联合利巴韦林治疗48周似乎比治疗24周更有效。