Clinical trial data analysis using R
著者
書誌事項
Clinical trial data analysis using R
（Chapman & Hall/CRC biostatistics series）（A Chapman & Hall book）
CRC Press, c2011
- : hardback
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注記
Bibliography: p. 349-357
Includes index
内容説明・目次
内容説明
Too often in biostatistical research and clinical trials, a knowledge gap exists between developed statistical methods and the applications of these methods. Filling this gap, Clinical Trial Data Analysis Using R provides a thorough presentation of biostatistical analyses of clinical trial data and shows step by step how to implement the statistical methods using R. The book's practical, detailed approach draws on the authors' 30 years of real-world experience in biostatistical research and clinical development.
Each chapter presents examples of clinical trials based on the authors' actual experiences in clinical drug development. Various biostatistical methods for analyzing the data are then identified. The authors develop analysis code step by step using appropriate R packages and functions. This approach enables readers to gain an understanding of the analysis methods and R implementation so that they can use R to analyze their own clinical trial data.
With step-by-step illustrations of R implementations, this book shows how to easily use R to simulate and analyze data from a clinical trial. It describes numerous up-to-date statistical methods and offers sound guidance on the processes involved in clinical trials.
目次
Introduction to R
What Is R?
Steps on Installing R and Updating R Packages
R for Clinical Trials
A Simple Simulated Clinical Trial
Concluding Remarks
Overview of Clinical Trials
Introduction
Phases of Clinical Trials and Objectives
The Clinical Development Plan
Biostatistical Aspects of a Protocol
Treatment Comparisons in Clinical Trials
Data from Clinical Trials
Statistical Models for Treatment Comparisons
Data Analysis in R
Treatment Comparisons in Clinical Trials with Covariates
Data from Clinical Trials
Statistical Models Incorporating Covariates
Data Analysis in R
Analysis of Clinical Trials with Time-to-Event Endpoints
Clinical Trials with Time-to-Event Data
Statistical Models
Statistical Methods for Right-Censored Data
Statistical Methods for Interval-Censored Data
Step-by-Step Implementations in R
Analysis of Data from Longitudinal Clinical Trials
Clinical Trials
Statistical Models
Analysis of Data from Longitudinal Clinical Trials
Sample Size Determination and Power Calculation in Clinical Trials
Prerequisites for Sample Size Determination
Comparison of Two Treatment Groups with Continuous Endpoints
Two Binomial Proportions
Time-to-Event Endpoint
Design of Group Sequential Trials
Longitudinal Trials
Relative Changes and Coefficient of Variation: An Extra
Meta-Analysis of Clinical Trials
Data from Clinical Trials
Statistical Models for Meta-Analysis
Meta-Analysis of Data in R
Bayesian Analysis Methods in Clinical Trials
Bayesian Models
R Packages in Bayesian Modeling
MCMC Simulations
Bayesian Data Analysis
Analysis of Bioequivalence Clinical Trials
Data from Bioequivalence Clinical Trials
Bioequivalence Clinical Trial Endpoints
Statistical Methods to Analyze Bioequivalence
Step-by-Step Implementation in R
Analysis of Adverse Events in Clinical Trials
Adverse Event Data from a Clinical Trial
Statistical Methods
Step-by-Step Implementation in R
Analysis of DNA Microarrays in Clinical Trials
DNA Microarray
Breast Cancer Data
Bibliography
Index
Concluding Remarks appear at the end of each chapter.
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