首页> 外文期刊>Liver international : >Predicting efficacy and safety outcomes in patients with hepatitis C virus genotype 1 and persistently 'normal' alanine aminotransferase levels treated with peginterferon alpha-2a (40KD) plus ribavirin.
【24h】

Predicting efficacy and safety outcomes in patients with hepatitis C virus genotype 1 and persistently 'normal' alanine aminotransferase levels treated with peginterferon alpha-2a (40KD) plus ribavirin.

机译:预测使用聚乙二醇干扰素α-2a(40KD)加利巴韦林治疗的丙型肝炎病毒基因型1和持续“正常”丙氨酸氨基转移酶水平的患者的疗效和安全性结果。

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

BACKGROUND: Currently, the approved dosage of ribavirin has not been studied in patients with 'normal' alanine aminotransferase (ALT) levels. METHODS: Modelling and simulations were performed using generalised additive models (GAMs) to predict the incidence of anaemia and rate of sustained virological response (SVR) in patients with hepatitis C virus (HCV) genotype 1 and persistently 'normal' ALT levels treated with peginterferon alpha-2a (40KD) 180 microg/week plus ribavirin 1000/1200 mg/day for 48 weeks. RESULTS: Model-based simulations predicted that SVR rates would increase from 39 to 48% if patients with genotype 1 and persistently 'normal' ALT levels had received the standard weight-adjusted dose of ribavirin. This was similar to the predicted 49% SVR rate for genotype 1 patients with elevated ALT levels. The incidence of anaemia was predicted to increase from 13% to 23% in patients with persistently 'normal' ALT activity and was higher than that predicted for patients with elevated ALT levels; however, the difference appeared to be largely explained by the higher proportion of women in the former group. CONCLUSIONS: Simulations based on GAM suggest that regimens for patients with HCV genotype 1 should include the standard weight-adjusted dose of ribavirin, as similar SVR rates are predicted to be achieved, regardless of patients' ALT status at baseline.
机译:背景:目前,尚未对具有“正常”丙氨酸氨基转移酶(ALT)水平的患者研究利巴韦林的批准剂量。方法:使用通用加性模型(GAM)进行建模和模拟,以预测丙型干扰素治疗的丙型肝炎病毒(HCV)基因型和持续“正常” ALT水平患者的贫血发生率和持续病毒应答率(SVR) alpha-2a(40KD)180微克/周加上利巴韦林1000/1200毫克/天,持续48周。结果:基于模型的模拟预测,如果基因型1和持续“正常” ALT水平的患者接受了标准重量调整剂量的病毒唑,SVR率将从39%增至48%。这与ALT水平升高的基因型1患者的预期SVR率相似,为49%。 ALT持续“正常”的患者贫血的发生率预计将从13%增加到23%,高于ALT水平升高的患者的贫血发生率。但是,这种差异似乎主要是由于前一组中妇女所占比例较高所致。结论:基于GAM的模拟表明,HCV基因型1的患者的治疗方案应包括标准重量调整剂量的利巴韦林,因为无论患者在基线时的ALT状态如何,都有望达到相似的SVR率。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号