首页> 外文期刊>Journal of biopharmaceutical statistics >Statistical Evaluation of Several Methods for Cut-Point Determination of Immunogenicity Screening Assay
【24h】

Statistical Evaluation of Several Methods for Cut-Point Determination of Immunogenicity Screening Assay

机译:几种确定免疫原性筛选方法切点的方法的统计评估

获取原文
获取原文并翻译 | 示例
           

摘要

The cut point of the immunogenicity screening assay is the level of response of the immunogenicity screening assay at or above which a sample is defined to be positive and below which it is defined to be negative. The Food and Drug Administration Guidance for Industry on Assay Development for Immunogenicity Testing of Therapeutic recommends the cut point to be an upper 95 percentile of the negative control patients. In this article, we assume that the assay data are a random sample from a normal distribution. The sample normal percentile is a point estimate with a variability that decreases with the increase of sample size. Therefore, the sample percentile does not assure at least 5% false-positive rate (FPR) with a high confidence level (e.g., 90%) when the sample size is not sufficiently enough. With this concern, we propose to use a lower confidence limit for a percentile as the cut point instead. We have conducted an extensive literature review on the estimation of the statistical cut point and compare several selected methods for the immunogenicity screening assay cut-point determination in terms of bias, the coverage probability, and FPR. The selected methods evaluated for the immunogenicity screening assay cut-point determination are sample normal percentile, the exact lower confidence limit of a normal percentile (Chakraborti and Li, 2007) and the approximate lower confidence limit of a normal percentile. It is shown that the actual coverage probability for the lower confidence limit of a normal percentile using approximate normal method is much larger than the required confidence level with a small number of assays conducted in practice. We recommend using the exact lower confidence limit of a normal percentile for cut-point determination.
机译:免疫原性筛选测定的临界点是免疫原性筛选测定的反应水平,在该水平或高于该水平时,样品被定义为阳性,而在低于或低于该水平时,样品被定义为阴性。食品和药物管理局工业用药治疗性免疫原性检测分析开发指南建议,切点应为阴性对照患者的95%以上。在本文中,我们假设测定数据是来自正态分布的随机样本。样本法向百分位数是一个点估计,其变异性随样本大小的增加而减小。因此,当样本量不足时,样本百分位数不能确保具有高置信度(例如90%)的至少5%假阳性率(FPR)。考虑到这一点,我们建议对百分比使用较低的置信度限制作为切入点。我们已经对统计切点的估计进行了广泛的文献综述,并根据偏倚,覆盖率和FPR比较了几种用于免疫原性筛选测定切点确定的选定方法。为评估免疫原性筛选分析的临界点而选择的方法是:样品正常百分位数,正常百分位数的确切下限(Chakraborti和Li,2007)和正常百分位数的近似下限。结果表明,在实践中使用少量测定方法,使用近似正常方法对正常百分位数下限置信度的实际覆盖概率远大于所需置信度。我们建议使用标准百分位数的确切下置信限来确定切点。

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