Thong Vo Duy, Poovorawan Kittiyod, Tangkijvanich Pisit, Wasitthankasem Rujipat, Vongpunsawad Sompong, Poovorawan Yong
Center of Excellence in Clinical Virology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Intervirology. 2015;58(6):373-81. doi: 10.1159/000444366. Epub 2016 Mar 25.
We conducted a systematic review and meta-analysis of the influence of host and viral factors on the sustained virologic response (SVR) in hepatitis C virus genotype 6 (HCV-6) patients treated with pegylated interferon (PEG-IFN) and ribavirin (RBV).
Data were retrieved from Medline, Embase, PubMed and the Cochrane Library for 'genotype 6' studies published up to December 2014 and for abstracts from international scientific meetings. Inclusion criteria were efficacy of PEG-IFN+RBV based on SVR, 24- or 48-week therapy and treatment-naïve patients. Patients with hepatitis B, D and E and HIV coinfection or another concurrent liver disease were excluded. Pooled standard difference, odds ratio and confidence intervals (CIs) were calculated using a random-effect model with STATA 11.
Fourteen studies were included in the meta-analysis. The pooled SVR rate was 80% (95% CI: 0.78-0.83, p < 0.0001; I2 = 71.2%). SVR of the PEG-IFN+RBV-treated HCV-6 patients was markedly higher than that of HCV-1 patients (80.1 vs. 55.3%). The SVR rate was significantly higher for the 48- than the 24-week treatment, but not different among HCV-infected patients with rs12979860 and ss469415590 polymorphisms of the ILFN4 gene (80.6% CC vs. 66.7% non-CC, p = 0.593; 81.1% TT/TT vs. 60% non-TT/TT, p = 0.288). Gender and type of PEG-IFN did not affect SVR rates.
Treatment outcomes for HCV-6 patients are superior to those for HCV-1 patients and comparable to those of HCV-2 and HCV-3 patients, especially at 48 weeks. The level of fibrosis affects treatment outcome, but SVR rates are not significantly different between genders. IL28B and IFNL4 polymorphisms are not significantly associated with HCV-6 treatment outcome.
我们对宿主和病毒因素对接受聚乙二醇干扰素(PEG-IFN)和利巴韦林(RBV)治疗的丙型肝炎病毒6型(HCV-6)患者持续病毒学应答(SVR)的影响进行了系统评价和荟萃分析。
从Medline、Embase、PubMed和Cochrane图书馆检索截至2014年12月发表的关于“6型基因型”研究的数据以及国际科学会议的摘要。纳入标准为基于SVR的PEG-IFN+RBV疗效、24周或48周治疗以及初治患者。排除合并乙型、丁型和戊型肝炎以及HIV感染或其他并发肝病的患者。使用STATA 11软件的随机效应模型计算合并标准差、比值比和置信区间(CI)。
荟萃分析纳入了14项研究。合并SVR率为80%(95%CI:0.78-0.83,p<0.0001;I2=71.2%)。接受PEG-IFN+RBV治疗的HCV-6患者的SVR明显高于HCV-1患者(80.1%对55.3%)。48周治疗的SVR率显著高于24周治疗,但在ILFN4基因rs12979860和ss469415590多态性的HCV感染患者中无差异(CC型为80.6%对非CC型为66.7%,p=0.593;TT/TT型为81.1%对非TT/TT型为60%,p=0.288)。性别和PEG-IFN类型不影响SVR率。
HCV-6患者的治疗结果优于HCV-1患者,与HCV-2和HCV-3患者相当,尤其是在48周时。纤维化程度影响治疗结果,但不同性别之间的SVR率无显著差异。IL28B和IFNL4多态性与HCV-6治疗结果无显著关联。