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In a recently released, detailed 64-page report entitled “The State of Cancer Care in America 2015,” the American Society of Clinical Oncology (ASCO) provided readers with more than a snapshot of what cancer care looks like in America today. Depending on how one measures progress against cancer—e.g., the number of new drugs available to treat cancer, […]
Today the National Coalition for Cancer Survivorship (NCCS) joined the Health Care Payment Learning and Action Network and announced its goal in support of alternative payment models that will foster better, more patient-centered cancer care for the nation’s more than 14 million cancer survivors. NCCS Board Chair and cancer survivor, Michael Kappel, attended the inaugural […]
Twenty years ago, the National Coalition for Cancer Survivorship’s Imperatives for Quality Cancer Care advocated that “standards of cancer care should be driven by the quality of care.” By giving voice to the patient perspective, patient-reported outcomes (PROs) play a key role in assessing and improving the quality of care and, therefore, in setting these […]
This guest post is part of the 2015 Cancer Policy Matters “The Imperatives for Quality Cancer Care: 20 Years Later” blog series. The third principle from the Imperatives for Quality Cancer Care states, “Standards of cancer care should be driven by the quality of care, not only by the cost of care, and should include participation […]
Components of shared decision-making. #CTACSummit2015 pic.twitter.com/1yjm5MSwDC — Shelley Fuld Nasso (@sfuldnasso) March 3, 2015 Public meeting on breast cancer patient-focused drug dev. April 2, register now https://t.co/1OXRCdQvZM — NCCS – National Coalition for Cancer Survivorship (@CancerAdvocacy) March 2, 2015 "regard the cancer patient as autonomous individual who has the right 2B involved in decisions.." via […]
The following editorial appeared in The Cancer Letter on February 27, 2015 The recent announcement by the Innovation Center at the Center for Medicare and Medicaid Services regarding the launch of an Oncology Care Model is an important step toward patient-centered cancer care. In 2013, the Institute of Medicine released its report, “Delivering High-Quality Cancer […]
The second principle of the Imperatives for Quality Cancer Care states, “Quality cancer care should be available in a health care system whose standards and guidelines are developed in consideration of treating the whole person with cancer. Health care plans must regard the cancer patient as an autonomous individual who has the right to be involved in decisions about […]
Too Fast, or Too Slow? Public disagrees over pace of #FDA's new drug approvals https://t.co/gnvqJq56AH via @RAPSorg — ResearchAmerica (@ResearchAmerica) February 25, 2015 Everything I know about a good death I learned from my cat https://t.co/KeC5qEcynk — Shelley Fuld Nasso (@sfuldnasso) February 25, 2015 A Faster Way to Try Many Drugs on Many Cancers https://t.co/EFms6hYq3d […]
The National Coalition for Cancer Survivorship (NCCS), notes with sadness the passing of Phyllis Torda, a fierce advocate for patient-centered health care for more than 25 years. We at NCCS first came to know Phyllis when she was with Families USA as their Director of their Health and Social policies. Subsequently, we were very fortunate […]
“The good physician treats the disease; the great physician treats the patient who has the disease.” -William Osler Since the creation of the National Cancer Act in 1971, the medical establishment—and indeed our entire society—has taken up the powerful metaphor of a “war on cancer” as the approach to attacking and overcoming this dreaded disease. This […]
Survivorship Champions is a program for all clinicians and researchers, both oncology and primary care, who are interested in improving survivorship care and primary care’s role in caring for cancer survivors.
The NCCS Cancer Policy & Advocacy Team (CPAT) is a program for survivors and caregivers to learn about pressing policy issues that affect quality cancer care in order to be engaged as advocates in public policy around the needs of cancer survivors.
NCCS represents the millions of Americans who share a common experience – living with, through and beyond a cancer diagnosis. By sharing your story of how you have been touched by cancer, you are supporting the national cancer survivorship movement.
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Founder
Northeast Regional Cancer Institute
“Perhaps one of the most impactful collaborations in Dr. Brereton’s extraordinary career remains his early work and long friendship with Ellen Stovall. Through him, and in turn through the thousands of lives he has touched, Ellen’s work continues, and her mission lives on.”
—Karen M. Saunders
President, Northeast Regional Cancer Institute