Textbook of Clinical Trials in Oncology: A Statistical Perspective

This book provides a comprehensive foundation in statistical design, conduct, and analysis of clinical trials, with a focus on oncology. It covers innovative designs, real-world examples, and access to statistical code, making it essential for statisticians and investigators in this field.

Format: Hardback
Length: 626 pages
Publication date: 13 May 2019
Publisher: Taylor & Francis Ltd

The demand for educational resources among statisticians and investigators is on the rise, necessitating the creation of this comprehensive book. Its primary objective is to offer readers a solid foundation in the statistical design, execution, and analysis of clinical trials. Furthermore, it serves as a valuable guide for statisticians and investigators with limited clinical trial experience who aspire to pursue a career in this field.

The remarkable advancements in genetic and molecular technologies have transformed the landscape of drug development. In recent years, clinical trials have undergone a remarkable transformation, becoming increasingly sophisticated as they incorporate genomic studies and employ efficient designs such as basket and umbrella trials. This book provides the essential background and expert guidance for the innovative statistical design and analysis of clinical trials in oncology.

Key Features:

Cutting-edge topics with a suitable technical background: The book covers a range of contemporary topics, ensuring that readers have a strong foundation in the necessary technical aspects.

Built around case studies: Each chapter is centered around real-world case studies, providing a hands-on approach to learning. These case studies offer practical insights and help readers apply statistical concepts to real-world scenarios.

Real examples of flaws in previously reported clinical trials: The book highlights common errors and pitfalls in clinical trial reporting, enabling readers to avoid such errors in their own work.

Access to statistical code: The book includes access to statistical code, allowing readers to replicate and analyze the examples discussed in the text.

Chapters written by internationally recognized statisticians: The book features contributions from esteemed statisticians from academia and pharmaceutical companies, ensuring a high level of expertise and quality.

Carefully edited to ensure consistency: The chapters have been meticulously edited to maintain consistency in style, level, and approach, making it easy for readers to follow and understand the content.

Topics covered: The book encompasses a wide range of topics, including innovative phase I and II designs, trials in immune-oncology and rare diseases, and many more.

In conclusion, this book is a vital resource for statisticians, investigators, and anyone interested in advancing their knowledge and expertise in clinical trials. With its comprehensive coverage, practical examples, and expert guidance, it provides the necessary tools to design, execute, and analyze clinical trials with confidence and precision.

Weight: 1378g
Dimension: 184 x 260 x 40 (mm)
ISBN-13: 9781138083776