Meaningful within-patient change for clinical outcome assessments: model-based approach versus cumulative distribution functions.

IF 1.2 4区 医学 Q4 PHARMACOLOGY & PHARMACY
Jinma Ren, Andrew G Bushmakin, Paul R Cislo, Lucy Abraham, Joseph C Cappelleri, Robert H Dworkin, John T Farrar
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引用次数: 0

Abstract

Objectives: The FDA recommends the use of anchor-based methods and empirical cumulative distribution function (eCDF) curves to establish a meaningful within-patient change (MWPC) for a clinical outcome assessment (COA). In practice, the estimates obtained from model-based methods and eCDF curves may not closely align, although an anchor is used with both. To help interpret their results, we investigated and compared these approaches.

Methods: Both repeated measures model (RMM) and eCDF approaches were used to estimate an MWPC on a target COA. We used both real-life (ClinicalTrials.gov: NCT02697773) and simulated data sets that included 688 patients with up to six visits per patient, target COA (range 0 to 10), and an anchor measure on patient global assessment of osteoarthritis from 1 (very good) to 5 (very poor). Ninety-five percent confidence intervals for the MWPC were calculated by the bootstrap method.

Results: The distribution of the COA score changes affected the degree of concordance between RMM and eCDF estimates. The COA score changes from simulated normally distributed data led to greater concordance between the two approaches than did COA score changes from the actual clinical data. The confidence intervals of MWPC estimate based on eCDF methods were much wider than that by RMM methods, and the point estimate of eCDF methods varied noticeably across visits.

Conclusions: Our data explored the differences of model-based methods over eCDF approaches, finding that the former integrates more information across a diverse range of COA and anchor scores and provides more precise estimates for the MWPC.

临床结果评估的有意义的患者内部变化:基于模型的方法与累积分布函数。
目的:FDA推荐使用基于锚定的方法和经验累积分布函数(eCDF)曲线来建立临床结果评估(COA)的有意义患者内变化(MWPC)。实际上,尽管锚点与模型方法同时使用,但从基于模型的方法获得的估计值与eCDF曲线可能不会紧密对齐。为了帮助解释他们的结果,我们调查并比较了这些方法。方法:采用重复测量模型(RMM)和eCDF方法估计目标COA的MWPC。我们使用了真实的数据集(ClinicalTrials.gov: NCT02697773)和模拟数据集,包括688名患者,每位患者最多6次就诊,目标COA(范围0到10),以及患者骨关节炎总体评估的锚点测量,从1(非常好)到5(非常差)。采用自举法计算了MWPC的95%置信区间。结果:COA评分变化的分布影响RMM与eCDF估计的一致性程度。模拟正态分布数据的COA评分变化比实际临床数据的COA评分变化导致两种方法之间的一致性更大。基于eCDF方法的MWPC估计置信区间远宽于RMM方法,并且eCDF方法的点估计在不同的访问中差异显著。结论:我们的数据探讨了基于模型的方法与eCDF方法的差异,发现前者在不同范围的COA和锚点分数中整合了更多信息,并为MWPC提供了更精确的估计。
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来源期刊
Journal of Biopharmaceutical Statistics
Journal of Biopharmaceutical Statistics 医学-统计学与概率论
CiteScore
2.50
自引率
18.20%
发文量
71
审稿时长
6-12 weeks
期刊介绍: The Journal of Biopharmaceutical Statistics, a rapid publication journal, discusses quality applications of statistics in biopharmaceutical research and development. Now publishing six times per year, it includes expositions of statistical methodology with immediate applicability to biopharmaceutical research in the form of full-length and short manuscripts, review articles, selected/invited conference papers, short articles, and letters to the editor. Addressing timely and provocative topics important to the biostatistical profession, the journal covers: Drug, device, and biological research and development; Drug screening and drug design; Assessment of pharmacological activity; Pharmaceutical formulation and scale-up; Preclinical safety assessment; Bioavailability, bioequivalence, and pharmacokinetics; Phase, I, II, and III clinical development including complex innovative designs; Premarket approval assessment of clinical safety; Postmarketing surveillance; Big data and artificial intelligence and applications.
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