AcknowledgmentsIntroduction
Part I. Cancer Drugs: The Outcomes They Improve and at What PriceChapter 1. The Basics of Cancer Drugs: Cost, Benefit, Value Chapter 2. Surrogate Endpoints in Cancer: What Are They and Where Are They Used? Chapter 3. The Use and Misuse of Surrogate Endpoints for Drug Approvals Chapter 4. How High Prices Harm Patients and Society
Part II. Societal Forces That Distort Cancer MedicineChapter 5. Hype, Spin, and the Unbridled Enthusiasm That Distorts Cancer MedicineChapter 6. Financial Conflict of InterestChapter 7. The Harms of Financial Conflicts and How to Rehabilitate MedicineChapter 8. Will Precision Oncology Save Us?
Part III. How to Interpret Cancer Evidence and TrialsChapter 9. Study Design 201Chapter 10. Principles of Oncology PracticeChapter 11. Important Trials in OncologyChapter 12. Global Oncology
Part IV. SolutionsChapter 13. How Should Cancer Drug Development Proceed?Chapter 14. What Can Three Federal Agencies Do Tomorrow? Chapter 15. What Can People with Cancer Do?Chapter 16. What Can Students, Residents, and Fellows Do?
Epilogue: The Hallmarks of Successful Cancer PolicyGlossary ReferencesIndex