首页> 美国卫生研究院文献>World Journal of Gastroenterology >Combination of low-dose ribavirin and interferon alfa-2a therapy followed by interferon alfa-2a monotherapy in chronic HCV-infected non-responders and relapsers after interferon alfa-2a monotherapy
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Combination of low-dose ribavirin and interferon alfa-2a therapy followed by interferon alfa-2a monotherapy in chronic HCV-infected non-responders and relapsers after interferon alfa-2a monotherapy

机译:低剂量利巴韦林和干扰素α-2a疗法联合干扰素α-2a单一疗法治疗慢性丙型肝炎病毒感染无反应者和复发后的复发者

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摘要

>AIM: To report on the efficacy, safety and tolerability of interferon alfa-2a combined with a “low dose” of ribavirin for relapsers and non-responders to alpha interferon monotherapy.>METHODS: Thirty four chronic hepatitis C virus infected non responders to interferon alfa-2a monotherapy (a course of at least 3 months treatment) and 13 relapsers to interferon alfa-2a monotherapy (a dose of 3 to 6 million units three times per week for at least 20 weeks but not more than 18 months) were treated with the same dose of interferon alfa-2a used before (3 to 6 million units three times per week) and ribavirin (10 mg/kg daily) for 6 months. In complete responders, interferon alfa-2a was administered for further 6 months at the same dose used before as monotherapy.>RESULTS: Seven (20.6%) of 34 non responders stopped the combined therapy due to adverse events, including two patients with histological and clinical Child A cirrhosis. In 17/27 (63%) non responders, the combined therapy was stopped after three months because of non response. Ten of the 27 non responders completed the 12 month treatment course. At a mean follow up of 28 months (16-37 months) after the treatment, 4/10 (15%) previous non responders still remained complete responders. All 13 previous relapsers completed the 12-month treatment course. At a mean follow up of 22 months (9-36 months) after treatment, 6/13 (46%) the previous relapsers were still sustained complete responders.>CONCLUSION: Our treatment schedule of the combined therapy for 6 months of interferon alfa-2a with a low dose of ribavirin (10 mg/kg/day) followed by 6 months of interferon alfa-2a monotherapy is able to induce a sustained complete response rate in 15% of non responders and 46% of relapsers with chronic hepatitis C virus related liver diseases comparable to those obtained with the standard doses of ribavirin 1000-1200 mg/day. Randomized prospective controlled trials using lower total amounts of ribavirin in combination with interferon should be performed.
机译:>目标:报告干扰素alfa-2a联合“低剂量”利巴韦林对α干扰素单一疗法的复发者和无效者的疗效,安全性和耐受性。>方法:有34例慢性丙型肝炎病毒感染无反应者接受干扰素alfa-2a单一疗法(至少3个月的疗程),并有13例复发者接受干扰素alfa-2a单一疗法(每周3次,剂量为3至600万单位)至少20周但不超过18个月)用之前使用的相同剂量的干扰素alfa-2a(每周3次至3至600万单位)和利巴韦林(每天10 mg / kg)治疗6个月。在完全缓解的患者中,干扰素alfa-2a以单药治疗前的相同剂量再服药6个月。>结果:34名非缓解患者中有7(20.6%)因不良事件而停止了联合治疗,包括两名在组织学和临床上均患有儿童A型肝硬化的患者。在17/27(63%)无反应者中,由于无反应,在三个月后停止联合治疗。 27位无反应者中有10位完成了为期12个月的治疗过程。治疗后平均随访28个月(16-37个月),之前有4/10(15%)的无反应者仍为完全反应者。之前所有13位复发者均完成了为期12个月的治疗过程。治疗后平均随访22个月(9-36个月),以前的复发者中有6/13(46%)仍然是完全缓解的患者。>结论:我们的联合治疗方案低剂量利巴韦林(10 mg / kg /天)的6个月干扰素α-2a继之6个月干扰素α-2a单一疗法能够在15%的无反应者和46%的无反应者中引起持续的完全缓解率。与慢性丙型肝炎病毒相关的肝病复发者可与标准剂量的利巴韦林1000-1200毫克/天获得的复发者相媲美。应进行使用较低总量的利巴韦林联合干扰素的随机前瞻性对照试验。

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