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You are here: Home1 / Policy2 / Quality Cancer Care

Quality Cancer Care

Our mission is to advocate for quality cancer care for all people touched by cancer, but what exactly is “quality cancer care,” and why is it essential for patients and the health care system? The National Academy of Medicine (formerly Institute of Medicine) and others have worked to define quality cancer care. NCCS has represented patient perspectives in these efforts and played a leadership role in building the evidence base for quality cancer care.

NCCS believes that cancer patients should have access to:

  • Care that adheres to evidence-based guidelines;
  • Comprehensive cancer care that assures treatment of the symptoms and side effects of cancer and cancer treatment;
  • Coordinated care with strong communication among all providers and the patient;
  • A written care plan detailing all elements of cancer care;
  • Care in a clinical trial, if it represents a potential treatment option;
  • Shared decision-making, including honest discussion about prognosis, the intent of therapy and the patient’s values and preferences regarding care;
  • Support for psychosocial needs;
  • Palliative care throughout the course of treatment, from diagnosis through end of life;
  • End-of-life care, including but not limited to hospice care;
  • Post-treatment survivorship care, including a survivorship care plan with a treatment summary and personalized recommendations for monitoring and follow-up care.
  • Robust health information systems that support and improve all other aspects of quality cancer care.

Ensuring quality cancer care is complex, and there are many areas for improvement and policy action. An important gap is in treatment decision-making and coordination of the multiple facets of cancer care. To address this gap, NCCS advocates to ensure that every cancer patient has access to cancer care planning and coordination. These services provide cancer patients information to make informed decisions about treatments, encourage collaboration among the multi-disciplinary cancer care providers, and facilitate transitions from active treatment to survivorship.

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Making sense of cancer screening updates

December 21, 2011
As experts alter course on guidelines for cancer screenings such as mammograms and the prostate-specific antigen test, the general…
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HHS to give states more flexibility to implement health reform

December 16, 2011
The Department of Health and Human Services today released a bulletin outlining proposed policies that will give states more flexibility…
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Manufacturing problems responsible for shortages of cancer drugs, says Government Accountability Office

December 16, 2011
The Government Accountability Office (GAO) has released its report on the state of shortages for cancer drugs and other conditions…
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Drug scarcity’s dire cost, and some ways to cope

December 14, 2011
When Jenny Morrill, who has been battling ovarian cancer since 2007, went to the hospital for her scheduled chemotherapy treatment…
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When care is worth it, even if end is death

December 14, 2011
An essay by Peter Bach, M.D. Twenty years ago, I helped save a man’s life. I met him in the emergency room of the hospital, just…
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Status as a grandfathered health plan

August 16, 2010
Patient Protection and Affordable Care Act NCCS endorsed Cancer Leadership Council comments The Honorable Kathleen Sebelius Secretary Department…
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Dependent coverage of children to age 26

August 11, 2010
Patient Protection and Affordable Care Act The Honorable Kathleen Sebelius Secretary Department of Health and Human Services 200 Independence…
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Cancer ‘always in the back of my mind’ for 3-time survivor

July 14, 2010
NCCS volunteer and Super Advocate, Jasan Zimmerman, is featured in a CNN Health article about childhood cancer survivors. The article…
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Policy

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    • Quality Cancer Care
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    • 2020 State of Cancer Survivorship Survey
    • Cancer Care Planning and Communications Act (CCPCA)

Latest News

Webinar – Survivorship at Atrium Health Wake Forest Baptist Comprehensive Cancer Center: Creating a Practical Workflow

May 12, 2023
The National Coalition for Cancer Survivorship (NCCS) hosted a Survivorship Champions webinar about survivorship care implementation,…
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Sandra Finestone, PsyD: Be Bold and Don’t Hesitate – A 30-year Survivor’s Advice on Advocacy

May 8, 2023
Advocate Spotlight: Sandra Finestone, PsyD A cancer diagnosis can be overwhelming and life-changing, but for Sandra Finestone, it…
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Accessing COVID-19 Resources After the Public Health Emergency Ends

May 4, 2023
The COVID-19 public health emergency (PHE), which has been in effect since early 2020, will end on May 11, 2023. The federal government…
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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.

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  • About
    • Our Mission
    • Our History
    • The 1986 Club
    • Our Team
      • Policy Advisors
    • Employment
    • Partnerships
    • Financial Information
  • Policy
    • Quality Cancer Care
    • Access to Care
    • Health Equity
    • Redefining Functional Status (RFS)
    • State of Survivorship Survey
      • 2022 Survey
      • 2021 Survey
      • 2020 Survey
    • Cancer Care Planning and Communications Act (CCPCA)
  • Get Involved
    • What is Advocacy?
    • Cancer Policy and Advocacy Team (CPAT)
    • Advocate Engagement Opportunities
    • Survivorship Champions
    • Subscribe to NCCS Updates
    • Elevating Survivorship
    • Survivor Stories
    • Cancerversary
    • State-Based Cancer Advocacy
  • Resources
    • COVID-19 Resources for Cancer Survivors
    • Survivorship Checklist
    • Cancer Survival Toolbox
    • Cancer Rehabilitation
    • Integrative Oncology
    • Publications
      • Talking With Your Doctor
      • Self Advocacy
      • Employment Rights
      • Remaining Hopeful
    • Telehealth
    • Taking Charge of Your Care
    • Care Planning for Cancer Survivors
    • Tools For Care Providers
    • Order Our Resources
  • News
  • Events
    • Ellen L. Stovall Award
      • 2022 Winners
      • Awardees
      • Reception and Sponsorship
      • Committees
      • Nominations
    • Cancer Policy Roundtable (CPR)
      • Fall 2022 CPR
      • Spring 2022 CPR
      • Fall 2021 CPR
      • Spring 2021 CPR
      • Fall 2020 CPR
      • Spring 2020 CPR
    • Cancer Policy and Advocacy Team (CPAT) Virtual Symposium 2022
    • 2022 State of Survivorship Survey Results
    • Webinars
  • Contact Us

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Harmar Brereton, MD

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