Hepatobiliary Division, Department of Internal Medicine, College of Medicine, Kaohsiung Medical University, Taiwan.
J Gastroenterol Hepatol. 2010 Apr;25(4):758-65. doi: 10.1111/j.1440-1746.2009.06148.x.
A number of hepatitis C virus (HCV) patients without a rapid virological response (RVR) achieved a sustained virological response (SVR) with peginterferon-alpha-2a/ribavirin. The aim of this study was to identify factors associated with SVR in non-RVR patients.
Baseline and on-treatment factors were used to explore the prognostic factors for SVR in 113 HCV genotype-1 (HCV-1) and 20 HCV-2 non-RVR patients in two randomized trials.
The SVR rate in HCV-1 patients with a complete early virological response (cEVR) and partial early virological response was 91.9% versus 45% (P < 0.001) and 21.4% versus 10% (P = 0.62), respectively, after 48 and 24 weeks of treatment. The SVR rate in HCV-2 patients with a cEVR was 90.9% versus 57.1% (P = 0.25), respectively, after 24 and 16 weeks of treatment. Multivariate analysis showed that cEVR and standard regimen were independently associated with SVR. Viral kinetic study revealed that HCV viral loads < 10,000 IU/mL at week 4 were the best predictor of cEVR for both HCV-1 and HCV-2 non-RVR patients with the accuracy of 81% and 95%, respectively, and also of SVR with the accuracy of 78% and 92%, respectively, in patients receiving standard of care. The most important independent predictors for cEVR were HCV viral loads < 10(4) IU/mL at week 4, followed by increased ribavirin dose within 12 weeks of treatment.
Achieving a cEVR with standard of care is the most important predictor of SVR in non-RVR patients. Week 4 viral loads < 10,000 IU/mL could accurately predict cEVR early and following SVR in non-SVR patients.
许多未达到快速病毒学应答(RVR)的丙型肝炎病毒(HCV)患者经聚乙二醇干扰素-α-2a/利巴韦林治疗后获得持续病毒学应答(SVR)。本研究旨在确定非 RVR 患者获得 SVR 的相关因素。
采用基线和治疗期间的因素,对两项随机试验中 113 例 HCV 基因型 1(HCV-1)和 20 例 HCV-2 非 RVR 患者进行了 SVR 的预测因素分析。
在治疗 48 和 24 周后,HCV-1 患者中完全早期病毒学应答(cEVR)和部分早期病毒学应答患者的 SVR 率分别为 91.9%和 45%(P<0.001)和 21.4%和 10%(P=0.62);HCV-2 患者中 cEVR 的 SVR 率分别为 90.9%和 57.1%(P=0.25),治疗 24 和 16 周后。多变量分析显示,cEVR 和标准方案与 SVR 独立相关。病毒动力学研究显示,HCV-1 和 HCV-2 非 RVR 患者治疗第 4 周时 HCV 病毒载量<10000IU/ml 是 cEVR 的最佳预测因素,准确性分别为 81%和 95%,且对标准治疗患者的 SVR 预测准确性分别为 78%和 92%。cEVR 的最重要的独立预测因素是治疗第 4 周时 HCV 病毒载量<10(4)IU/ml,其次是治疗 12 周内增加利巴韦林剂量。
标准治疗方案下获得 cEVR 是预测非 RVR 患者 SVR 的最重要指标。第 4 周时 HCV 病毒载量<10000IU/ml 可以早期准确预测非 RVR 患者的 cEVR 及其随后的 SVR。