首页> 外文期刊>Journal of Medical Virology >A matched case-controlled study of 48 and 72 weeks of peginterferon plus ribavirin combination therapy in patients infected with HCV genotype 1b in Japan: amino acid substitutions in HCV core region as predictor of sustained virological response.
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A matched case-controlled study of 48 and 72 weeks of peginterferon plus ribavirin combination therapy in patients infected with HCV genotype 1b in Japan: amino acid substitutions in HCV core region as predictor of sustained virological response.

机译:在日本对感染HCV基因型1b的患者进行的聚乙二醇干扰素联合利巴韦林联合治疗48和72周的病例对照研究:HCV核心区域的氨基酸取代可作为持续病毒学应答的预测指标。

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摘要

Substitution of amino acid (aa) 70 and 91 in the core region of HCV genotype 1b is a useful pretreatment predictor of efficacy of 48-week peginterferon (PEG-IFN) plus ribavirin (RBV) therapy. Here, we determined the efficacy of 72-week PEG-IFN/RBV and the predictive factors to such therapy in a case-control study matched for sex, age, and periods from the start of treatment to initial point of HCV RNA-negative. We compared the treatment efficacy of 72-week regimen in 65 patients with that of 48-week in 130 patients, who were infected with HCV genotype 1b and treated with PEG-IFN/RBV. They consisted mainly of late virological responders (LVR) (HCV RNA-positive at 12 weeks and negative at 24 weeks after start of treatment). Sustained virological response (SVR) was achieved by 61.5% and 32.3% of patients of the 72- and 48-week groups, respectively, while non-virological response was noted in 9.2% and 29.2% of the respective groups. Multivariate analysis identified substitution of aa 70 and 91 (Arg70 and/or Leu91) and duration of treatment (72-week) as independent parameters that significantly influenced SVR. For Arg70 and/or Leu91 of core region, SVR rate was significantly higher in 72- (68.0%) than 48-week group (37.8%). For wild-type of ISDR, SVR rate was significantly higher in 72- (61.2%) than in 48-week group (29.3%). We conclude that 72-week PEG-IFN/RBV improves SVR rate for LVR, especially those with Arg70 and/or Leu91 of core region or wild-type of ISDR. Substitution of aa 70 and 91 is also a useful pretreatment predictor of response to 72-week PEG-IFN/RBV.
机译:HCV基因型1b核心区域氨基酸(aa)70和91的取代是48周聚乙二醇干扰素(PEG-IFN)联合利巴韦林(RBV)治疗功效的有用的预处理预测指标。在这里,我们在一项病例对照研究中确定了72周PEG-IFN / RBV的疗效以及这种治疗的预测因素,该研究根据性别,年龄和从治疗开始到HCV RNA阴性起始点的时期进行了匹配。我们比较了感染HCV基因型1b并用PEG-IFN / RBV治疗的65例患者的72周方案与130例患者的48周方案的疗效。它们主要由晚期病毒应答者(LVR)组成(治疗开始后12周时HCV RNA阳性,而24周时阴性)。在72周和48周组中,分别有61.5%和32.3%的患者获得了持续的病毒学应答(SVR),而在相应组中,分别有9.2%和29.2%的患者获得了非病毒学应答。多变量分析确定了aa 70和91(Arg70和/或Leu91)的取代以及治疗时间(72周)是显着影响SVR的独立参数。对于核心区域的Arg70和/或Leu91,72-(68.0%)的SVR率显着高于48周组(37.8%)。对于野生型ISDR,SVR率在72周(61.2%)显着高于48周组(29.3%)。我们得出的结论是72周的PEG-IFN / RBV可以提高LVR的SVR率,尤其是那些具有Arg70和/或Leu91核心区域或ISDR野生型的患者。氨基酸70和91的取代也可作为对72周PEG-IFN / RBV反应的有用的预处理预测指标。

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