Departamento de Gastroenterología, Hospital de Especialidades, Centro Médico Nacional Siglo XXI, IMSS, Av. Cuauhtemoc 330, Col. Doctores, 06725, Mexico, DF, Mexico.
Dig Dis Sci. 2010 Sep;55(9):2629-35. doi: 10.1007/s10620-009-1062-3. Epub 2009 Dec 4.
With only a third of Latinos achieving sustained virologic response (SVR), there is a need for enhanced HCV treatment. Amantadine has been proposed to improve response rates in addition to standard therapy with peginterferon alpha and ribavirin. Our objective is to evaluate whether triple therapy with amantadine improves SVR rates in this special population.
Treatment-naïve Latino subjects with HCV genotype 1 infection were randomized to receive peginterferon alpha-2a plus weight-based ribavirin for 48 weeks (double therapy) or the same regimen plus amantadine 200 mg daily (triple therapy). The primary endpoint was SVR. Predictors of liver fibrosis using APRI and Forns indices were also evaluated.
We enrolled 124 patients with chronic hepatitis C genotype 1. Sixty-three received conventional therapy and 61 patients had triple therapy with amantadine. SVR at week 72 was achieved in 25 patients (39.7%) vs. 26 patients (42.6%) in the double and triple regimen, respectively (p=0.561). After multivariate analysis, advanced fibrosis, obesity, and low pretreatment ALT levels were associated with non-response in both groups (p=0.0234, p=0.0012, p=0.0249, respectively). APRI values delimited an area under the ROC curve (AUROC) of 0.724 and Forns index with AUROC of 0.733. There was no difference between both indices in predicting significant fibrosis (Knodell index: F3-F4).
Our study demonstrates that the addition of amantadine to standard treatment of chronic HCV does not improve SVR rates in Latino patients with genotype 1. Further research to improve response rates in this special population is needed.
仅有三分之一的拉丁裔患者达到持续病毒学应答(SVR),因此需要增强 HCV 治疗。金刚烷胺已被提议用于提高标准治疗(聚乙二醇干扰素α和利巴韦林)的应答率。我们的目的是评估在这种特殊人群中,金刚烷胺三联疗法是否能提高 SVR 率。
我们将 HCV 基因型 1 感染的治疗初治拉丁裔患者随机分配接受聚乙二醇干扰素α-2a 联合基于体重的利巴韦林治疗 48 周(双药治疗)或相同方案联合金刚烷胺 200mg 每日(三药治疗)。主要终点是 SVR。还评估了使用 APRI 和 Forns 指数预测肝纤维化的情况。
我们共纳入了 124 例慢性丙型肝炎基因型 1 患者。63 例接受常规治疗,61 例接受金刚烷胺三联治疗。第 72 周的 SVR 在双药和三药治疗组中分别为 25 例(39.7%)和 26 例(42.6%)(p=0.561)。多变量分析后,两组中晚期纤维化、肥胖和低预处理 ALT 水平与无应答相关(p=0.0234、p=0.0012、p=0.0249)。APRI 值划定了 ROC 曲线下的面积(AUROC)为 0.724,Forns 指数的 AUROC 为 0.733。两种指数在预测显著纤维化(Knodell 指数:F3-F4)方面没有差异。
我们的研究表明,在拉丁裔基因型 1 患者中,金刚烷胺联合标准治疗不能提高 SVR 率。需要进一步研究以提高该特殊人群的应答率。