Composite Plot for Visualizing Aminotransferase and Bilirubin Changes in Clinical Trials of Subjects with Abnormal Baseline Values

IF 4 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Bereket Tesfaldet, Tejas Patel, Minjun Chen, Frank Pucino, Lilliam Rosario, Paul Hayashi, Eileen Navarro Almario
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引用次数: 0

Abstract

Introduction

On-treatment excursions of liver laboratory test values in clinical trials involving subjects with underlying liver disease are relevant for the efficacy and safety assessment of drug products and biologics. Existing visualization and analysis tools do not efficiently provide an integrated view of these excursions when baseline liver tests are abnormal.

Objective

The aim of this study was to develop a composite plot that enables visualization of on-treatment changes in liver test results both as multiples of the upper limit of normal defined by each laboratory’s reference population (×ULN) and multiples of the subjects’ baseline (×BLN) values.

Methods

The composite plot approach combines biochemical evaluation for drug-induced severe hepatotoxicity (eDISH) plots sequentially applied to subjects’ baseline and peak on-treatment liver test results normalized by ULN and integrates them into a four-panel shift plot of peak on-treatment values normalized by BLN.

Results

The composite plot enabled efficient assessment of improvement in liver test values during treatment compared with pretreatment in subjects treated with the investigational drug (or the natural history of placebo-treated subjects) and identified outlier subjects for potential drug-induced liver injury.

Conclusion

For studies in subjects with abnormal baseline values, the composite plot has potential application in the assessment of beneficial and concerning on-treatment modifications in liver test values in reference to the individual subject’s baseline and population threshold values.

Abstract Image

用于显示基线值异常受试者临床试验中转氨酶和胆红素变化的复合图
导言:在涉及患有基础肝病的受试者的临床试验中,肝脏实验室检测值在治疗期间的偏移与药物产品和生物制剂的疗效和安全性评估息息相关。现有的可视化和分析工具不能有效地提供基线肝脏检测异常时这些偏移的综合视图。本研究的目的是开发一种复合图,它既能以各实验室参考人群定义的正常值上限的倍数(×ULN),也能以受试者基线值的倍数(×BLN)来显示治疗中肝脏检测结果的变化。方法该复合图谱方法将药物诱导重度肝毒性生化评估(eDISH)图谱依次应用于按 ULN 归一化的受试者基线和治疗时肝脏检测结果峰值,并将其整合到按 BLN 归一化的治疗时峰值的四面板移动图谱中。结论对于基线值异常的受试者的研究,复合图具有潜在的应用价值,可以参照受试者个体的基线值和群体阈值,评估治疗期间肝脏检测值的有益和相关变化。
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来源期刊
Drug Safety
Drug Safety 医学-毒理学
CiteScore
7.60
自引率
7.10%
发文量
112
审稿时长
6-12 weeks
期刊介绍: Drug Safety is the official journal of the International Society of Pharmacovigilance. The journal includes: Overviews of contentious or emerging issues. Comprehensive narrative reviews that provide an authoritative source of information on epidemiology, clinical features, prevention and management of adverse effects of individual drugs and drug classes. In-depth benefit-risk assessment of adverse effect and efficacy data for a drug in a defined therapeutic area. Systematic reviews (with or without meta-analyses) that collate empirical evidence to answer a specific research question, using explicit, systematic methods as outlined by the PRISMA statement. Original research articles reporting the results of well-designed studies in disciplines such as pharmacoepidemiology, pharmacovigilance, pharmacology and toxicology, and pharmacogenomics. Editorials and commentaries on topical issues. Additional digital features (including animated abstracts, video abstracts, slide decks, audio slides, instructional videos, infographics, podcasts and animations) can be published with articles; these are designed to increase the visibility, readership and educational value of the journal’s content. In addition, articles published in Drug Safety Drugs may be accompanied by plain language summaries to assist readers who have some knowledge of, but not in-depth expertise in, the area to understand important medical advances.
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