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预测聚乙二醇干扰素-α2a 和利巴韦林治疗慢性丙型肝炎基因型 1 患者在治疗 4、8 和 12 周后的非 SVR。

Prediction of nonSVR to therapy with pegylated interferon-alpha2a and ribavirin in chronic hepatitis C genotype 1 patients after 4, 8 and 12 weeks of treatment.

机构信息

The Mina and Everard Goodman Faculty of Life Sciences, Bar-Ilan University, Ramat Gan, Israel.

出版信息

J Viral Hepat. 2010 May;17(5):345-51. doi: 10.1111/j.1365-2893.2009.01183.x. Epub 2009 Sep 25.

Abstract

In patients with chronic hepatitis C genotype 1, the current algorithm for treatment discontinuation is based on no early virological response (<2 log decline in hepatitis C virus (HCV)-RNA) at 12 weeks. It is important to determine whether prediction of nonsustained virological response (NR) before 12 weeks can be robustly obtained by statistical methods. We used longitudinal discriminant analysis (LDA) to build and cross-validate models including baseline patient characteristics and measurements of serum HCV-RNA in the first 4, 8 or 12 weeks of treatment. The performance of each model was evaluated by the partial AUC (PA) index, exploring the accuracy of prediction in the range of high negative predictive values. Models were compared by computing 95% confidence intervals for the difference in PA indices. NR was best predicted before week 12 by a single HCV-RNA measurement at week 8 taken together with gender, BMI and age (W8 model, PA index = 0.857). This model was not inferior to models that included a measurement at week 12 (PA index = 0.831). The best model obtained with LDA within the first 4 weeks, which included measurements at days 4, 8 and at week 4, was found to be inferior to the week 8 model (PA index = 0.796). These results indicate that lack of sustained viral response is best predicted after 8 weeks of treatment and that waiting until 12 weeks does not improve the prediction.

摘要

在慢性丙型肝炎基因型 1 患者中,目前的治疗停药算法基于在 12 周时无早期病毒学应答(HCV-RNA 下降<2 对数)。重要的是要确定是否可以通过统计方法可靠地获得 12 周之前非持续病毒学应答(NR)的预测。我们使用纵向判别分析(LDA)构建并交叉验证了包括基线患者特征和治疗前 4、8 或 12 周内血清 HCV-RNA 测量值的模型。通过部分 AUC(PA)指数评估每个模型的性能,探索高阴性预测值范围内预测的准确性。通过计算 PA 指数差异的 95%置信区间来比较模型。通过在第 8 周时单次 HCV-RNA 测量值与性别、BMI 和年龄(W8 模型,PA 指数=0.857)相结合,在第 12 周之前可以最佳预测 NR。该模型并不逊于包含第 12 周测量值的模型(PA 指数=0.831)。在最初的 4 周内通过 LDA 获得的最佳模型,其中包括第 4、8 天和第 4 周的测量值,发现不如第 8 周的模型(PA 指数=0.796)。这些结果表明,在治疗 8 周后最好预测持续病毒反应缺乏,等待至 12 周并不能改善预测。

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