临床前肿瘤生长抑制研究中的实验设计考虑因素和统计分析。

IF 1.3 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pharmaceutical Statistics Pub Date : 2024-06-10 DOI:10.1002/pst.2399
Vinicius Bonato, Szu-Yu Tang, Matilda Hsieh, Yao Zhang, Shibing Deng
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引用次数: 0

摘要

动物模型用于癌症临床前研究,以确定药物靶点、为临床试验选择候选化合物、确定最佳药物剂量、确定生物标志物并确保化合物的安全性。本教程旨在概述动物研究的研究设计和数据分析,重点是用于确定抗癌化合物优先次序的肿瘤生长抑制(TGI)研究。本教程讨论的一些实验设计方面的问题包括:选择适当的生物模型、选择用于评估抗癌活性的终点(肿瘤体积、肿瘤生长率、事件或分类终点)、考虑与这类研究相关的测量误差和潜在偏差、样本量估计以及讨论缺失数据的处理。教程还回顾了 TGI 研究中采用的统计分析方法,既考虑了在单个时间点收集的连续终点,也考虑了在多个时间点纵向收集的连续终点。此外,还讨论了针对事件发生(如动物死亡或肿瘤大小达到某一阈值)的研究进行的时间到事件分析。此外,对于涉及分类终点的 TGI 研究,本教程还概述了统计方法,以便有效比较不同治疗组的结果。最后,本教程还讨论了在 TGI 研究中评估联合用药协同作用的分析方法,这涉及联合用药以提高总体疗效。本教程还包括 R 示例脚本,以帮助用户对该主题进行相关数据分析。
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Experimental design considerations and statistical analyses in preclinical tumor growth inhibition studies.

Animal models are used in cancer pre-clinical research to identify drug targets, select compound candidates for clinical trials, determine optimal drug dosages, identify biomarkers, and ensure compound safety. This tutorial aims to provide an overview of study design and data analysis from animal studies, focusing on tumor growth inhibition (TGI) studies used for prioritization of anticancer compounds. Some of the experimental design aspects discussed here include the selection of the appropriate biological models, the choice of endpoints to be used for the assessment of anticancer activity (tumor volumes, tumor growth rates, events, or categorical endpoints), considerations on measurement errors and potential biases related to this type of study, sample size estimation, and discussions on missing data handling. The tutorial also reviews the statistical analyses employed in TGI studies, considering both continuous endpoints collected at single time-point and continuous endpoints collected longitudinally over multiple time-points. Additionally, time-to-event analysis is discussed for studies focusing on event occurrences such as animal deaths or tumor size reaching a certain threshold. Furthermore, for TGI studies involving categorical endpoints, statistical methodology is outlined to compare outcomes among treatment groups effectively. Lastly, this tutorial also discusses analysis for assessing drug combination synergy in TGI studies, which involves combining treatments to enhance overall treatment efficacy. The tutorial also includes R sample scripts to help users to perform relevant data analysis of this topic.

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来源期刊
Pharmaceutical Statistics
Pharmaceutical Statistics 医学-统计学与概率论
CiteScore
2.70
自引率
6.70%
发文量
90
审稿时长
6-12 weeks
期刊介绍: Pharmaceutical Statistics is an industry-led initiative, tackling real problems in statistical applications. The Journal publishes papers that share experiences in the practical application of statistics within the pharmaceutical industry. It covers all aspects of pharmaceutical statistical applications from discovery, through pre-clinical development, clinical development, post-marketing surveillance, consumer health, production, epidemiology, and health economics. The Journal is both international and multidisciplinary. It includes high quality practical papers, case studies and review papers.
期刊最新文献
Beyond the Fragility Index. A Model-Based Trial Design With a Randomization Scheme Considering Pharmacokinetics Exposure for Dose Optimization in Oncology. Potential Bias Models With Bayesian Shrinkage Priors for Dynamic Borrowing of Multiple Historical Control Data. Subgroup Identification Based on Quantitative Objectives. A Bayesian Dynamic Model-Based Adaptive Design for Oncology Dose Optimization in Phase I/II Clinical Trials.
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