首页> 外文期刊>Journal of viral hepatitis. >Accurate model predicting sustained response at week 4 of therapy with pegylated interferon with ribavirin in patients with chronic hepatitis C.
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Accurate model predicting sustained response at week 4 of therapy with pegylated interferon with ribavirin in patients with chronic hepatitis C.

机译:准确的模型可预测聚乙二醇干扰素联合病毒唑治疗慢性丙型肝炎患者在治疗第4周的持续反应。

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Current models used to predict response to peginterferon plus ribavirin treatment, based on viral decline during the first 12 weeks of therapy, have focused on creating an early stopping rule to avoid unnecessary prolongation of therapy. We developed a multivariate model that predicted sustained virological response and nonresponse at baseline and during the first 12 weeks of therapy using collected data from 186 unselected patients with chronic hepatitis C treated with peginterferon plus ribavirin. This model employed ordinal regression with similarity least squares technology to assign the probability of a given outcome. Model variables include sex, age, prior treatment status, genotype, baseline serum alanine aminotransferase levels, histologic necroinflammation and fibrosis scores and serum hepatitis C virus RNA concentration at baseline and weeks, 4, 8, and 12. A multivariate model demonstrated high performance values at all time points. At baseline, the model demonstrated a negative predictive value (NPV) and a positive predictive value (PPV) of 91% and 95%, respectively. At week 4, these values improved to 97% and 100%, respectively, with 95% sensitivity, 89% specificity and 93% accuracy. At week 4, the model was equally efficient for naive or previously treated patients. Internal validation demonstrated 90% PPV, 94% NPV, 95% sensitivity, 88% specificity and 92% accuracy. A week 4 stopping rule for patients with chronic hepatitis C treated with peginterferon with ribavirin might be proposed by using the model developed in our study.
机译:基于在治疗的前12周期间病毒下降,目前用于预测对聚乙二醇干扰素加利巴韦林治疗的反应的模型,其重点已放在创建早期停止规则上,以避免不必要的治疗延长。我们开发了一个多变量模型,该模型使用收集的186例接受非聚乙二醇干扰素加利巴韦林治疗的慢性丙型肝炎患者的收集数据,预测了基线和治疗前12周的持续病毒学应答和无应答。该模型采用序数回归和相似度最小二乘技术分配给定结果的概率。模型变量包括性别,年龄,以前的治疗状态,基因型,基线血清丙氨酸氨基转移酶水平,组织学坏死性炎症和纤维化评分以及基线,第4、8和12周时的丙型肝炎病毒RNA浓度。多变量模型显示出较高的性能值在所有时间点。在基线时,模型显示的负预测值(NPV)和正预测值(PPV)分别为91%和95%。在第4周,这些值分别提高到97%和100%,灵敏度为95%,特异性为89%,准确度为93%。在第4周,该模型对于天真的或先前接受过治疗的患者同样有效。内部验证显示90%的PPV,94%的NPV,95%的敏感性,88%的特异性和92%的准确性。使用我们研究中开发的模型,可能会建议接受聚乙二醇干扰素联合利巴韦林治疗的慢性丙型肝炎患者第4周停止治疗的规则。

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