Slavenburg Serena, Weggelaar Ines, van Oijen Martijn G H, Drenth Joost P H
Department of Medicine, Division of Gastroenterology and Hepatology, Radboud University Nijmegen Medical Centre, Nijmegen, the Netherlands.
Antivir Ther. 2009;14(8):1139-48. doi: 10.3851/IMP1464.
Current guidelines recommend a duration of 24 weeks of treatment with pegylated interferon and ribavirin for patients infected with chronic hepatitis C virus (HCV) genotypes 2 and 3. Several trials investigated whether shorter treatment duration is equally effective in achieving sustained virological response (SVR). Our aim was to determine the optimal length of treatment in patients with HCV genotypes 2 and 3.
Systematic literature identified eight randomized controlled trials (RCTs). Meta-analyses were carried out on SVR data from three studies randomized at baseline and five studies randomized at rapid virological response (RVR) to either 12-16 weeks or a 24-week course.
Pooled SVR data were higher in standard treatment in RCTs that randomized at baseline, with a relative risk (RR) of 0.88 (95% confidence interval [CI] 0.76-1.01). The pooled proportion of SVR rates of RCTs that randomized at RVR were similar in the short treatment group (82%) as in the standard treatment (83%), with the pooled effect given by a RR of 1.00 (95% CI 0.92-1.09).
A shorter course (12-16 weeks) of combination therapy does not impair efficacy compared with a 24-week course in HCV genotypes 2 and 3 patients who achieve an RVR. HCV patients without RVR should consider 24 weeks of treatment.
当前指南推荐,对于慢性丙型肝炎病毒(HCV)2型和3型感染患者,采用聚乙二醇化干扰素和利巴韦林治疗24周。多项试验研究了较短疗程治疗在实现持续病毒学应答(SVR)方面是否同样有效。我们的目的是确定HCV 2型和3型患者的最佳治疗疗程。
系统文献检索确定了8项随机对照试验(RCT)。对3项基线随机分组研究和5项快速病毒学应答(RVR)时随机分组至12 - 16周或24周疗程的研究的SVR数据进行荟萃分析。
在基线随机分组的RCT中,标准治疗的汇总SVR数据更高,相对风险(RR)为0.88(95%置信区间[CI] 0.76 - 1.01)。在RVR时随机分组的RCT中,短疗程治疗组的SVR率汇总比例(82%)与标准治疗组(83%)相似,汇总效应的RR为1.00(95% CI 0.92 - 1.09)。
对于实现RVR的HCV 2型和3型患者,与24周疗程相比,较短疗程(12 - 16周)的联合治疗不会损害疗效。未实现RVR的HCV患者应考虑24周治疗。