Clinical trials in oncology

Author(s)

    • Green, Stephanie
    • Benedetti, Jacqueline
    • Crowley, John

Bibliographic Information

Clinical trials in oncology

Stephanie Green, Jacqueline Benedetti and John Benedetti

Chapman & Hall, 1997

Available at  / 7 libraries

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Description and Table of Contents

Description

Clinical Trials in Oncology emphasizes the importance of proper study design and data management, and explains why communication and partnership between statisticians and clinicians are vital to the conduct of a successful clinical trial. Clinicians face considerable risks-subtle and ever present-when designing trials and interpreting data. This book deals with all aspects of successful trials in a manner accessible to clinicians. Topics addressed include advantages and disadvantages of multi-arm trials; pitfalls to avoid, such as analyzing survival by response or by dose; and how and whether meta-analyses are justified.

Table of Contents

Introduction A Brief History of Clinical Trials The Southwest Oncology Group Example Trials The Reason for This Book Statistical Concepts Introduction The Phase II Trial - Estimation The Phase III Trial - Hypthesis Testing The Proportional Hazards Model Sample Size Calculations The Design of Clinical Trials Introduction Endpoints Phase I Trials Phase II Trials Phase III Trials Conclusion Multi-Arm Trials Introduction Types of Multi-Arm Trials Significance Level Power Interaction Other Model Assumptions To Screen or Not To Screen Timing of Randomization Conclusion Interim Analysis and Data Monitoring Committees Planned Interim Analyses Data Monitoring Committees: Rationale and Responsibilities Monitoring Committees: Composition Examples Concluding Remarks Data Management and Quality Control Introduction: Why Worry? Protocol Development Basic Data Items Data Forms Protocol Management and Evaluation Quality Assurance Audits Training Database Management Conclusion Appendix: Examples Reporting of Results Timing of Report Required Information Analyses Pitfalls Introduction Historical Controls Competing Risks Outcome by Outcome Analyses Subset Analyses Surrogate Endpoints Exploratory Analyses Introduction Some Background and Notation Identification of Prognostic Factors Forming Prognostic Groups Meta-Analysis Concluding Remarks Summary and Conclusions.

by "Nielsen BookData"

Details

  • NCID
    BA33966960
  • ISBN
    • 0412996316
  • Country Code
    uk
  • Title Language Code
    eng
  • Text Language Code
    eng
  • Place of Publication
    London
  • Pages/Volumes
    x, 203 p.
  • Size
    24cm
  • Classification
  • Subject Headings
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