COPD随机试验中FEV1和加重率的联合纵向模型meta分析。

IF 2.2 4区 医学 Q3 PHARMACOLOGY & PHARMACY
Carolina Llanos-Paez, Claire Ambery, Shuying Yang, Misba Beerahee, Elodie L Plan, Mats O Karlsson
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引用次数: 0

摘要

基于模型的荟萃分析(MBMA)是一种整合来自异质设计随机对照试验(rct)的相关汇总水平数据的方法。本研究不仅评估了已发表的MBMA对慢性阻塞性肺疾病(COPD)患者一秒钟用力呼气量(FEV1)的可预测性及其与年加重率的关系,还纳入了新的随机对照试验的数据。还对所有药物进行了比较有效性分析。汇总水平数据来自2013年7月至2020年11月发表的随机对照试验(n = 132篇参考文献,包括156项研究),并结合传统MBMA中使用的数据(截至2013年7月发表的随机对照试验- n = 142)。扩充后的数据(n = 298)使用拟合优度图评估已发表的MBMA的预测性能。此外,将2013年7月之前未上市的药物纳入模型,估计了一组新的参数。传统的MBMA模型可以很好地预测2013年后的FEV1数据,新的估计参数与同类药物的估计参数相似。然而,加重模型高估了2013年后的年平均加重率数据。纳入治疗前安慰剂率研究开始的年份改善了模型的预测性能,这可能解释了随着时间的推移疾病管理的潜在改善。将新数据添加到传统COPD MBMA中,使模型更加稳健,在终点FEV1和平均年加重率方面都具有更高的可预测性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Joint longitudinal model-based meta-analysis of FEV<sub>1</sub> and exacerbation rate in randomized COPD trials.

Joint longitudinal model-based meta-analysis of FEV<sub>1</sub> and exacerbation rate in randomized COPD trials.

Joint longitudinal model-based meta-analysis of FEV<sub>1</sub> and exacerbation rate in randomized COPD trials.

Joint longitudinal model-based meta-analysis of FEV1 and exacerbation rate in randomized COPD trials.

Model-based meta-analysis (MBMA) is an approach that integrates relevant summary level data from heterogeneously designed randomized controlled trials (RCTs). This study not only evaluated the predictability of a published MBMA for forced expiratory volume in one second (FEV1) and its link to annual exacerbation rate in patients with chronic obstructive pulmonary disease (COPD) but also included data from new RCTs. A comparative effectiveness analysis across all drugs was also performed. Aggregated level data were collected from RCTs published between July 2013 and November 2020 (n = 132 references comprising 156 studies) and combined with data used in the legacy MBMA (published RCTs up to July 2013 - n = 142). The augmented data (n = 298) were used to evaluate the predictive performance of the published MBMA using goodness-of-fit plots for assessment. Furthermore, the model was extended including drugs that were not available before July 2013, estimating a new set of parameters. The legacy MBMA model predicted the post-2013 FEV1 data well, and new estimated parameters were similar to those of drugs in the same class. However, the exacerbation model overpredicted the post-2013 mean annual exacerbation rate data. Inclusion of year when the study started on the pre-treatment placebo rate improved the model predictive performance perhaps explaining potential improvements in the disease management over time. The addition of new data to the legacy COPD MBMA enabled a more robust model with increased predictability performance for both endpoints FEV1 and mean annual exacerbation rate.

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来源期刊
CiteScore
4.90
自引率
4.00%
发文量
39
审稿时长
6-12 weeks
期刊介绍: Broadly speaking, the Journal of Pharmacokinetics and Pharmacodynamics covers the area of pharmacometrics. The journal is devoted to illustrating the importance of pharmacokinetics, pharmacodynamics, and pharmacometrics in drug development, clinical care, and the understanding of drug action. The journal publishes on a variety of topics related to pharmacometrics, including, but not limited to, clinical, experimental, and theoretical papers examining the kinetics of drug disposition and effects of drug action in humans, animals, in vitro, or in silico; modeling and simulation methodology, including optimal design; precision medicine; systems pharmacology; and mathematical pharmacology (including computational biology, bioengineering, and biophysics related to pharmacology, pharmacokinetics, orpharmacodynamics). Clinical papers that include population pharmacokinetic-pharmacodynamic relationships are welcome. The journal actively invites and promotes up-and-coming areas of pharmacometric research, such as real-world evidence, quality of life analyses, and artificial intelligence. The Journal of Pharmacokinetics and Pharmacodynamics is an official journal of the International Society of Pharmacometrics.
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