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复杂研究设计数据的纵向暴露-反应建模面临的挑战:以对克罗恩病患者使用优特克单抗的CDAI评分建模为例

Challenges in longitudinal exposure-response modeling of data from complex study designs: a case study of modeling CDAI score for ustekinumab in patients with Crohn's disease.

作者信息

Hu Chuanpu, Adedokun Omoniyi J, Chen Yang, Szapary Philippe O, Gasink Christopher, Sharma Amarnath, Zhou Honghui

机构信息

Global Clinical Pharmacology, Janssen Research & Development, LLC, 1400 McKean Road, PO Box 776, Spring House, PA, 19477, USA.

Clinical Immunology, Janssen Research & Development, LLC, 1400 McKean Road, PO Box 776, Spring House, PA, 19477, USA.

出版信息

J Pharmacokinet Pharmacodyn. 2017 Oct;44(5):425-436. doi: 10.1007/s10928-017-9529-x. Epub 2017 Jun 16.

DOI:10.1007/s10928-017-9529-x
PMID:28623612
Abstract

Informative exposure-response modeling of clinical endpoints is important in drug development to identify optimum dose and dosing regimens. Despite much recent progress in mechanism-based longitudinal modeling of clinical data, challenges remain in clinical trials of diseases such as Crohn's disease, where a commonly used composite endpoint Crohn's Disease Activity Index (CDAI) has considerable variation in its administration and scoring between different assessors and complex study designs typically include maintenance phases with randomized withdrawal re-randomizations and other response driven dose adjustments. This manuscript illustrates the complexities of exposure-response modeling of such composite endpoint data through a latent-variable based Indirect Response model framework for CDAI scores using data from three phase III trials of ustekinumab in patients with moderate-to-severe Crohn's Disease. Visual predictive check was used to evaluate model performance. Potential impacts of the study design on model development and evaluation of the E-R relationship in the induction and maintenance phases of treatment are discussed. Certain biases appeared difficult to overcome, and an autocorrelated residual error model was found to provide improvement.

摘要

临床终点的信息性暴露-反应建模在药物研发中对于确定最佳剂量和给药方案至关重要。尽管近期在基于机制的临床数据纵向建模方面取得了很大进展,但在克罗恩病等疾病的临床试验中仍存在挑战,在这些试验中,常用的综合终点克罗恩病活动指数(CDAI)在不同评估者之间的管理和评分存在相当大的差异,而且复杂的研究设计通常包括维持阶段,有随机撤药再随机分组以及其他基于反应的剂量调整。本手稿通过基于潜变量的间接反应模型框架,使用乌司奴单抗治疗中度至重度克罗恩病患者的三项III期试验数据,阐述了此类综合终点数据暴露-反应建模的复杂性。采用可视化预测检查来评估模型性能。讨论了研究设计对治疗诱导期和维持期模型开发以及暴露-反应关系评估的潜在影响。某些偏差似乎难以克服,发现自相关残差误差模型可提供改进。

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