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慢性丙型肝炎患者的抗病毒治疗。

Antiviral therapy for patients with chronic hepatitis C.

作者信息

Heathcote J

机构信息

University of Toronto, University Health Network, Ontario, Canada.

出版信息

Semin Liver Dis. 2000;20(2):185-99. doi: 10.1055/s-2000-9941.

Abstract

Several large, randomized, controlled treatment trials in persons with hepatitis C and ongoing hepatitis have been reported recently. These have shown that, in patients without other comorbid conditions, treatment for from 6 to 12 months with a combination of interferon-alpha 2b, 3 MU three times a week (ttw), plus ribavirin, 1,000-1,200 mg daily, results in a higher incidence of sustained virologic response than does treatment with interferon-alpha 2b monotherapy, 3 MU ttw, given for similar durations. Patients who have relapsed after interferon monotherapy may achieve a sustained virologic response when retreated with interferon plus ribavirin for 6 months or when given a higher dose of interferon for a longer duration than the initial treatment. By contrast, patients who had no virologic response to prior interferon monotherapy have only a small chance of achieving a sustained response when similarly retreated. Although the efficacy of treatment for hepatitis C has improved steadily over the last decade, current interferon-based therapies still achieve a sustained virologic response in fewer than half of patients who initiate therapy, are associated with appreciable side effects, and are expensive. Furthermore, the natural history of chronic hepatitis C suggests that even in the absence of therapy, most patients with chronic hepatitis C infection may experience little morbidity or mortality for decades. Finally, published therapeutic trials stem largely from tertiary referral centers, where an especially high level of commitment is expected from both the patients and the team in charge of therapy. Typically, such trials have also excluded patients with comorbid diseases, thus reducing their "generalizability." This review focuses on two fundamental questions about the currently available treatments for this disease: Who should be treated with them? And when should they be treated? Critical analysis suggests that the answers to these questions are not as clear as they may superficially appear.

摘要

最近有多项针对丙型肝炎和活动性肝炎患者的大型随机对照治疗试验的报道。这些试验表明,在没有其他合并症的患者中,使用α-2b干扰素(300万单位,每周三次)联合利巴韦林(每日1000 - 1200毫克)治疗6至12个月,与使用相同疗程的α-2b干扰素单药治疗(300万单位,每周三次)相比,持续病毒学应答的发生率更高。干扰素单药治疗后复发的患者,再次使用干扰素联合利巴韦林治疗6个月,或给予比初始治疗更高剂量的干扰素并延长治疗时间,可能会实现持续病毒学应答。相比之下,之前对干扰素单药治疗无病毒学应答的患者,再次进行类似治疗时实现持续应答的机会很小。尽管在过去十年中丙型肝炎治疗的疗效稳步提高,但目前基于干扰素的疗法在开始治疗的患者中,仍只有不到一半能实现持续病毒学应答,且伴有明显的副作用,费用也很高。此外,慢性丙型肝炎的自然史表明,即使不进行治疗,大多数慢性丙型肝炎感染患者在几十年内可能很少出现发病或死亡情况。最后,已发表的治疗试验大多来自三级转诊中心,在这些中心,患者和负责治疗的团队都需要有特别高的投入。通常,此类试验也排除了合并其他疾病的患者,因此降低了其“普遍性”。本综述聚焦于关于该疾病现有治疗方法的两个基本问题:谁应该接受这些治疗?以及何时应该进行治疗?批判性分析表明,这些问题的答案并不像表面看起来那么清晰。

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