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聚乙二醇干扰素 α-2b 和利巴韦林治疗慢性丙型肝炎病毒(基因型 1 和 4 感染)的疗效。

Efficacy of pegylated interferon α-2b and ribavirin in chronic hepatitis C virus (genotypes 1 and 4) infection.

机构信息

*3rd Department of Paediatrics, Polish Mother's Memorial Hospital, Research Institute, Lodz †Department of Infectious Diseases and Hepatology, Collegium Medicum, Mikołaj Kopernik University, Bydgoszcz, Poland.

出版信息

J Pediatr Gastroenterol Nutr. 2013 Dec;57(6):694-9. doi: 10.1097/MPG.0b013e3182a7d91e.

Abstract

BACKGROUND AND OBJECTIVE

The course of chronic hepatitis C in children is often mild or asymptomatic, but may lead to liver cirrhosis and neoplasm. The aim of our study was retrospective evaluation of treatment efficacy using pegylated interferon (IFN)-α2b with ribavirin in children and adolescents with chronic hepatitis C, both treatment naïve and re-treated.

METHODS

The study comprised 79 patients with chronic hepatitis C ages 8 to 18 years (43 patients re-treated; 54 infected with genotype 1 hepatitis C virus and 25 with genotype 4), treated with pegylated IFN-α2b (1.5 μg · kg⁻¹ · week⁻¹) plus ribavirin (15 mg · kg⁻¹ · day⁻¹) for 48 weeks. The primary endpoint was sustained virologic response (SVR).

RESULTS

Early viral response (EVR) was observed in 43.1% and end-of-treatment response in 47.9% of patients. In 44.3% of patients, SVR was achieved, which was maintained for at least the next 6 months. Patients not treated before significantly more frequently attained EVR, end-of-treatment response, and SVR (64%, 65.6%, and 63.9%, respectively) as compared with re-treated patients (30%, 33.3%, and 27.9%, respectively). Among 28 patients who attained EVR, 23 achieved SVR. In 2 patients, despite lack of EVR, SVR was observed. There were numerous adverse effects. They were not so severe as to discontinue therapy.

CONCLUSIONS

Combined therapy with pegylated IFN-α2b and ribavirin in patients with chronic hepatitis C, infected with hepatitis C virus genotypes 1 and 4, was more effective in treatment-naïve patients (63.9%) as compared with re-therapy cases (27.9%). SVR was maintained for at least the next 6 months in all of the patients. The applied treatment has limited efficacy and evokes numerous adverse effects; thus, search for new methods of treatment is mandatory.

摘要

背景与目的

儿童慢性丙型肝炎的病程常为轻度或无症状,但可能导致肝硬化和肿瘤。本研究旨在回顾性评估聚乙二醇干扰素(IFN)-α2b 联合利巴韦林治疗初治和复治儿童和青少年慢性丙型肝炎的疗效。

方法

本研究纳入了 79 例年龄 8 至 18 岁的慢性丙型肝炎患者(43 例复治;54 例感染基因型 1 丙型肝炎病毒,25 例感染基因型 4),接受聚乙二醇干扰素-α2b(1.5μg·kg-1·week-1)联合利巴韦林(15mg·kg-1·day-1)治疗 48 周。主要终点为持续病毒学应答(SVR)。

结果

43.1%的患者出现早期病毒学应答(EVR),47.9%的患者出现治疗结束时应答。44.3%的患者获得 SVR,且至少在接下来的 6 个月内维持。与复治患者相比,未接受过治疗的患者更频繁地获得 EVR(64%比 30%)、治疗结束时应答(65.6%比 33.3%)和 SVR(63.9%比 27.9%)。在 28 例获得 EVR 的患者中,23 例获得 SVR。在 2 例患者中,尽管没有获得 EVR,但仍观察到 SVR。有许多不良反应,但并不严重到需要中断治疗。

结论

聚乙二醇干扰素-α2b 联合利巴韦林治疗感染基因型 1 和 4 丙型肝炎病毒的慢性丙型肝炎患者,在初治患者中的疗效(63.9%)优于复治患者(27.9%)。所有患者的 SVR 至少在接下来的 6 个月内维持。应用的治疗方法疗效有限,并引起许多不良反应,因此必须寻找新的治疗方法。

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