The second edition of Oncology Clinical Trials is a comprehensive guide to conducting and analyzing cancer clinical trials in the era of precision medicine. With the latest designs and methods for investigating the safety and efficacy of targeted therapies, immunotherapies, and combination therapies, this updated edition is essential for researchers, oncologists, and industry professionals involved in clinical trials.

This second edition has been thoroughly revised and expanded to include the most up-to-date information on the design and analysis of oncology clinical trials. Divided into six sections, the book covers everything from the principles governing clinical trials to the regulatory issues impacting domestic and global trials.

Written by a team of experts in the field, this book provides valuable insights and guidance on conducting clinical trials in a safe and effective manner. Real-world examples and case studies are included to illustrate the challenges and successes of conducting quality clinical trials.

The book begins with an introduction to the basic principles of clinical trials in oncology, including the ethical considerations and regulatory requirements. It then delves into the innovative statistical design methods used in oncology clinical trials, such as adaptive designs, genomics-based trials, and meta-analysis. The book also explores important topics like endpoint selection, biomarker testing, and cost-effectiveness analysis.

In addition to its comprehensive coverage of clinical trial design and analysis, this second edition also includes new chapters on immunotherapy trials, radiation therapy trials, multi-arm trials, and the use of genomics in clinical trials. These new chapters reflect the latest advancements in the field and provide readers with a deeper understanding of the current trends and challenges in oncology clinical trials.

One of the key strengths of this book is its focus on practical issues in clinical trial design and implementation. The authors provide practical tips and guidance on topics such as patient recruitment, data collection and management, and regulatory compliance. They also address the challenges of conducting international and global trials and offer insights into how to navigate these complex processes.

Throughout the book, there is a strong emphasis on the importance of patient-centered research and the need for collaboration among researchers, clinicians, and patients. The authors highlight the importance of patient-reported outcomes and quality-of-life measurements in clinical trials and provide guidance on how to incorporate these endpoints into study designs.

Overall, Oncology Clinical Trials is an essential resource for anyone involved in the design, conduct, and analysis of clinical trials in oncology. Its comprehensive coverage, practical approach, and real-world examples make it a valuable reference for researchers, oncologists, and industry professionals.

Order your copy of Oncology Clinical Trials today and join the global community of researchers and clinicians who are working to advance the field of oncology through innovative clinical trials.