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Malignant: How Bad Policy and Bad Evidence Harm People with Cancer

Malignant: How Bad Policy and Bad Evidence Harm People with Cancer

Autorzy
Wydawnictwo Johns Hopkins University Press
Data wydania 21/04/2020
Liczba stron 304
Forma publikacji książka w twardej oprawie
Poziom zaawansowania Dla profesjonalistów, specjalistów i badaczy naukowych
Język angielski
ISBN 9781421437637
Kategorie Zdrowie i bezpieczeństwo publiczne
162.75 PLN (z VAT)
$36.61 / €34.89 / £30.29 /
Produkt na zamówienie
Dostawa 3-4 tygodnie
Ilość
Do schowka

Opis książki

Each week, people read about new and exciting cancer drugs. Some of these drugs are truly transformative, offering major improvements in how long patients live or how they feel-but what is often missing from the popular narrative is that, far too often, these new drugs have marginal or minimal benefits. Some are even harmful. In Malignant, hematologist-oncologist Dr. Vinayak K. Prasad writes about the many sobering examples of how patients are too often failed by cancer policy and by how oncology is practiced. Throughout this work, Prasad illuminates deceptive practices which

* promote novel cancer therapies long before credible data are available to support such treatment; and
* exaggerate the potential benefits of new therapies, many of which cost thousands and in some cases hundreds of thousands of dollars.

Prasad then critiques the financial conflicts of interest that pervade the oncology field, the pharmaceutical industry, and the US Food and Drug administration.

This is a book about how the actions of human beings-our policies, our standards of evidence, and our drug regulation-incentivize the pursuit of marginal or unproven therapies at lofty and unsustainable prices. Prasad takes us through how cancer trials are conducted, how drugs come to market, and how pricing decisions are made, asking how we can ensure that more cancer drugs deliver both greater benefit and a lower price. Ultimately, Prasad says,

* more cancer clinical trials should measure outcomes that actually matter to people with cancer;
* patients on those trials should look more like actual global citizens;
* we need drug regulators to raise, not perpetually lower, the bar for approval; and
* we need unbiased patient advocates and experts.

This well-written, opinionated, and engaging book explains what we can do differently to make serious and sustained progress against cancer-and how we can avoid repeating the policy and practice mistakes of the past. Malignant is punchy and persuasive, and the author is clearly in command of his subject matter. Prasad offers valuable advice on how to keep up with research as well as the appropriate way to analyse clinical trial reports. -- Talha K Burki * The Lancet Hematology * Aimed at general readers (including patients), oncology trainees and experts in health-care policy, it informs and disturbs throughout. -- Andrew Robinson * Nature * Patients should ask their oncologist how good the cure is: do I really live longer and better than doing "nothing"? Let them start by asking whether their doctor has read Prasad's book. * Zurich Weekly News Review * [Malignant is] so applicable to the issues of the pandemic . . . Because what we're seeing is a research infrastructure that is not set up to do rapid evaluation, and to be resilient and to respond to a health crisis. -- Marty Makary, MD, MPH * MedPage Today *

Malignant: How Bad Policy and Bad Evidence Harm People with Cancer

Spis treści

Acknowledgments

Introduction



Part I. Cancer Drugs: The Outcomes They Improve and at What Price

Chapter 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 Medicine

Chapter 5. Hype, Spin, and the Unbridled Enthusiasm That Distorts Cancer Medicine

Chapter 6. Financial Conflict of Interest

Chapter 7. The Harms of Financial Conflicts and How to Rehabilitate Medicine

Chapter 8. Will Precision Oncology Save Us?



Part III. How to Interpret Cancer Evidence and Trials

Chapter 9. Study Design 201

Chapter 10. Principles of Oncology Practice

Chapter 11. Important Trials in Oncology

Chapter 12. Global Oncology



Part IV. Solutions

Chapter 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 Policy

Glossary

References

Index

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