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Fotolia 23428619 S e1461260836640

Reps. DeSaulnier and Poe Introduce Bipartisan “Cancer Care Planning and Communications Act”

March 8, 2018/in Cancer News, Cancer Policy Blog, NCCS News Access to Care, Care Planning, Clinical Guidelines, Health Care Coverage, Quality Cancer Care, Shared Decision-Making NCCS News /by actualize
Advocated for by NCCS, the bill would increase comprehensive cancer care planning for millions of Medicare beneficiaries.  Washington, D.C. – Today, Rep. Mark DeSaulnier (D-CA) and Rep. Ted Poe (R-TX), both cancer survivors and co-chairs of the Congressional Cancer Survivors Caucus, introduced H.R. 5160, the Cancer Care Planning and Communications (CCPC) Act.

A longtime legislative priority of the National Coalition for Cancer Survivorship, the bill would create a Medicare code to reimburse providers for time and resources used to create cancer care plans for Medicare beneficiaries.

“The Cancer Care Planning and Communications Act is a tangible way to significantly improve the quality of care for cancer patients in Medicare,” said NCCS CEO Shelley Fuld Nasso.  “Care plans before, during, and after treatment encourage communication between providers and patients, and help alleviate some anxiety at every phase of the care continuum. The CCPC Act would empower patients with tools to manage and coordinate their care from active treatment throughout survivorship. NCCS and our partners look forward to working with Reps. DeSaulnier and Poe to move the CCPC Act forward.”

“Medical breakthroughs are at an all-time high, but advancements in doctor-patient communications are not keeping pace. We know that less than half of all cancer patients feel adequately informed about their diagnosis. Without a written plan explaining treatments and expected symptoms, patients are often left with more questions than answers. As a cancer survivor, who is grateful to have a healthy and full life ahead of me, I hope that my experience and this legislation will help others better navigate a diagnosis,” said Congressman Mark DeSaulnier.

“Cancer is an epidemic in our country. Approximately 1.7 million Americans will be diagnosed with cancer this year alone. As a cancer survivor myself, I know how difficult it can be to understand what the plan for a patients’ treatment is,” said Congressman Ted Poe. “This legislation takes a positive step forward by incentivizing doctors to help their patients understand their planned cancer care path and giving them the peace of mind, all cancer patients, and their families deserve.”

“As a cancer survivor, I know firsthand how important having a care plan is to receiving the best care possible,” said Lee Jones, a cancer survivor. “A care plan is not only critical to fostering communication between a patient and doctor, but it serves as a roadmap in helping navigate the difficult process of cancer diagnosis, treatment choices, and treatment management. This is particularly true for older survivors on Medicare, who also are dealing with risk of recurrence, secondary cancers and other health issues.  I am proud to support the passage of the Cancer Care Planning and Communications Act, and hope it is quickly passed by Congress to help make sure all patients receive the best care possible.”

“We commend the Congressional Cancer Survivors co-chairs for advancing this important legislation,” said Donald L. Trump, MD, FACP, CEO and Executive Director of the Inova Schar Cancer Institute. “The data show clearly that personalized and coordinated care leads to better outcomes—including longer survival! Based on these data, our center is designed as a facility where patients will have a single location to see their interdisciplinary team—medical , surgical and radiation oncologists, nutritionist, genetic and psychosocial counselors, all collaborating on a personalized plan for each patient, a treatment plan specific to the genomics and proteomics of their tumor, specific to their pharmacogenomics as appropriate and a survivorship plan to maximize the chance for survival and good health following treatment. Cancer care is more and more complicated—and successful; it is critical that physicians and patients be full partners in their treatment, that the overall plan of treatment and post-treatment care be fully developed and communicated—that’s what the Cancer Care Planning and Communications Act is promoting.”

Patient and professional organizations supporting the CCPC Act:

American College of Surgeons Commission on Cancer; American Society of Clinical Oncology; Association of Community Cancer Centers; Association of Oncology Social Work; Cancer Legal Resource Center; Cancer Support Community; College of American Pathologists; Colon Cancer Alliance; Critical Mass; Fight Colorectal Cancer; Hematology Oncology Pharmacy Association; International Myeloma Foundation; Lacuna Loft; LIVESTRONG; Lung Cancer Alliance; LUNGevity Foundation; Lymphoma Research Foundation; National Brain Tumor Society; National Patient Advocate Foundation; Oncology Nursing Society; Pancreatic Cancer Action Network; Stupid Cancer; The Children’s Cause for Cancer Advocacy; The Leukemia & Lymphoma Society; Triage Cancer; West Virginia Oncology Society; Zero Prostate Cancer.

Cancer centers supporting the CCPC Act:

City of Hope National Medical Center; Dana-Farber Cancer Institute; Georgetown Lombardi Comprehensive Cancer Center; Laura and Isaac Perlmutter Cancer Center at NYU Langone;
Loma Linda University Cancer Center; Masonic Cancer Center; Memorial Sloan-Kettering Cancer Center; Moffitt Cancer Center; Norris Cotton Cancer Center; Rutgers Cancer Institute
Stanford Cancer Institute; The University of Kansas Cancer Center; The University of Kentucky Markey Cancer Center; The University of Texas MD Anderson Cancer Center; The University of Virginia Cancer Center; UC Davis Comprehensive Cancer Center.

# # #

Find more CCPC Act information and advocacy tools for contacting Congress ».

Tags: cancer care, Cancer Survivorship, care planning, CCPC Act, clinical guidelines, Decision-Making, Medicare
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  • About
    • Our Mission
    • Our History
    • Our Leadership
      • Policy Advisors
    • Employment
    • Partnerships
    • Financial Information
  • Policy
    • Quality Cancer Care
    • Access to Care
    • Health Equity
    • Redefining Functional Status (RFS)
    • 2020 State of Cancer Survivorship Survey
    • Cancer Care Planning and Communications Act (CCPCA)
  • Get Involved
    • What is Advocacy?
    • Cancer Policy and Advocacy Team (CPAT)
    • Elevating Survivorship
    • Survivor Stories
    • Cancerversary
    • State Based Cancer Advocacy
  • Resources
    • COVID-19 Resources for Cancer Survivors
    • Survivorship Checklist
    • Cancer Survival Toolbox
    • Telehealth
    • Survivorship Champions
    • Publications
      • Talking With Your Doctor
      • Self Advocacy
      • Employment Rights
      • Remaining Hopeful
    • Cancer Convos Podcast
    • Taking Charge of Your Care
    • Care Planning for Cancer Survivors
    • Tools For Care Providers
    • Order Our Resources
  • News
  • Events
    • Ellen L. Stovall Award
      • Nominations
      • Honorees
      • Sponsors
      • Committees
    • From Shadows to Life: A Biography of the Cancer Survivorship Movement
    • Cancer Policy Roundtable
      • Spring 2021 Cancer Policy Roundtable
      • Fall 2020 Cancer Policy Roundtable
      • Spring 2020 Cancer Policy Roundtable
    • Cancer Policy and Advocacy Team (CPAT) Symposium 2020
    • 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