January News: CCCA's 2017 Policy Agenda

CCCA Outlines Policy Goals and Priorities for 2017

The 2017 policy agenda for CCCA addresses the most significant barriers to care along the continuum of the childhood cancer journey: access to care; the availability of treatments; and the post-treatment survivorship landscape.

Among our many policy plans in 2017:

  • Urge Congress to modify current PREA and BPCA language to accelerate and modernize childhood cancer drug development by providing FDA with more flexibility to apply PREA and BPCA where the science warrants pediatric studies.
  • Pursue the creation of a public-private drug development business model to identify and develop new therapies for children with cancer.
  • Urge Congress to support increases in NIH and NCI funding in order to accommodate expanded treatment development and clinical trials for pediatric cancer.
  • Urge Congress to pass the Childhood Cancer STAR Act, with a particular focus on the survivorship provisions that we have long championed.
  • Produce a comprehensive assessment of childhood cancer patient demographics identifying access to care and financial burdens.
  • Strengthen the Children's Health Insurance Program, and ensure that Medicaid/CHIP provide necessary access to care for childhood cancer patients.
  • Urge Congress to pass the Advancing Care for Exceptional Kids Act.

Read our full policy agenda online.

Related: If you missed our 2016 year-in-review, catch up on our blog!


TAKE ACTION: Weigh in on Healthcare Reform

As Congress moves to repeal the Affordable Care Act, we are asking families who have been impacted by childhood cancer to tell Congress about your insurance needs and concerns. Use our webform to contact your Members of Congress and urge them not to repeal the ACA without a responsible replacement plan in place. 

As a member of the Cancer Leadership Council, we signed on to a letter to Congress in December, urging due caution as changes to the Affordable Care Act are considered in the coming legislative session. More recently, we sent a letter to the co-chairs of the Congressional Childhood Cancer Caucus.

"We urge policymakers to protect children and adolescents with cancer and survivors as Congress considers the Affordable Care Act (ACA), Medicaid, and the Children's Health Insurance Program (CHIP). These programs currently cover over 40 million children and adolescents in our country, and any changes must consider the impact on these vulnerable populations. Specifically, any structural or policy reforms should not diminish coverage or access for children with cancer.

... Children in need of active treatment and appropriate symptom management, as well as survivors who need ongoing care including monitoring, follow-up services, and preventive services, could be adversely affected by significant disruptions in the insurance market. We support access to care for cancer patients across the continuum of their disease without a period of uncertainty in the insurance market that might result in loss of access to affordable insurance coverage and therefore access to care." (Full letter)


ALSO: Share Your Childhood Cancer Story with President Trump

We've launched an action alert to give you an opportunity to ensure that the new Administration understands the multitude of challenges facing children with cancer and childhood cancer survivors. Be a voice and share your story!


DIPG Awareness Resolution Introduced in Congress

Today, Representatives Steve Knight (R-CA) and Jackie Speier (D-CA) introduced the National DIPG Awareness Resolution. This legislation aims to raise awareness to the plight of childhood cancer through the lens of Diffuse Intrinsic Pontine Glioma (DIPG). It also calls for May 17, 2017 to be National DIPG Awareness Day.

This bill was drafted in part by our friend and colleague Janet Demeter, founder of Jack's Angels Foundation in Agua Dulce, California. We recognize and thank Janet for her hard work and for this tremendous achievement.

See the Jack's Angels press release for more details.


Recommended Reading {Quick Links}

The Blood-Brain BarrierCAC2 Webinar (1/26/17): The Coalition for Childhood Cancer (CAC2) presented its January 2017 all-member webinar onemerging technology using ultrasound and microbubbles to deliver therapeutic agents across the blood-brain barrier. 

How Precision Medicine Could be a Lifesaver for Kids with Brain CancerForbes (1/19/17): "The study, led by the Harvard-affiliated Dana-Farber/Boston Children's Cancer and Blood Disorders Centers, involved sequencing the genes of 200 tumor samples from children with brain cancer. The researchers found that 56% of the tumors had genetic abnormalities that could influence how the disease was diagnosed or treated by drugs already on the market or in clinical trials."

Biden to Tackle Broad Range of Cancer Issues, including Drug PricesThe Washington Post (1/4/17): "Vice President Biden, who led the Obama administration's 'cancer moonshot' initiative, will create a nonprofit organization to grapple with a broad range of cancer issues, including the high cost of cancer drugs, he said in an interview."

A New Urgency to Protect Survivors of Childhood Cancer, The Washington Post (12/25/16): "[Greg] Aune, like a growing number of scientists and clinicians, is focusing intently on 'late effects' of cancer treatments. Many of these researchers work in clinics designed specifically to monitor the health of childhood cancer survivors and alert them to potential risks. With the ranks of survivors swelling, there is an urgent need to understand the treatments' effects on the entire body, not just the tumor, and to come up with less-toxic therapies."

Jessica Kean
November Bulletin: Post-Election Edition

The Close of One Congress - and Preparing for Another

The election earlier this month surprised almost everyone. People across the country have since been adjusting both intellectually and emotionally as we move toward a Trump Administration and Republican control of both the House and Senate. The shock waves in Washington have been especially seismic, with policymakers recalibrating - and recalculating - how to position themselves and their agendas. 

The same is true for advocates committed to battling childhood cancer. While the goals of developing better treatments, access to care and quality survivorship remain, the outcome of the election changes many of the strategies and approaches.

One thing is certain, however: Families and patients dedicated to the fight will need to be even more focused, more engaged and more vocal. CCCA will be aggressively targeting any threats to the welfare of our kids and, as always, alerting advocates when they need to make their voices heard.

But before a new Congress and Administration take over in January, there is some urgent unfinished business in the current 'lame-duck' Congress. These are especially critical to childhood cancer advocates - and everyone will need to make their voices heard in the next couple of weeks.

Read on to find out more about these bills and what you can do to help ensure their passage in the final 13 work-days of this legislative session.


Register Now for our 12/8 Webinar: What Does the New Administration Mean for Childhood Cancer?

Don't miss this Children's Cause for Cancer Advocacy webinar, on the one month anniversary of the 2016 Election. Join us Thursday, December 8th at 5pm EST as we explore further what a Trump Administration could mean for childhood cancer, including:

  • The outlook for childhood cancer research;
  • The future of coverage for care;
  • How to become an effective advocate; and 
  • How to help us launch the CCCA Kids Action Network.

George Dahlman, CEO of Children's Cause, and Ziky Ababiya, Legislative Assistant for Rep. Chris Van Hollen will present, along with a to-be-named Republican counterpart.

Registration for this webinar is limited!

Reserve your spot today.


New York Event Exceeds Fundraising Goal: Thank you!

The Children's Cause was pleased to host another successful reception and silent auction at the James Burden Mansion in New York City earlier this month. We're so grateful to everyone who supported this year's event, which helps make our year-round advocacy work possible.

A highlight of the lovely evening was the presentation of the first Leonard M. Rosen Memorial Research Award. As pictured above, Adam Rosen presented the award to Mary McCabe, Director of the Cancer Survivorship Initiative at Memorial Sloan-Kettering Cancer Center. Ms. McCabe is widely recognized as a leader in cancer survivorship with the development of comprehensive programs for cancer survivors. In acknowledgement of the Award, Ms. McCabe will initiative a guest lectureship at MSK to focus on the ethics issues related to the development of new therapies for children including the issue of informed consent and specimen banks, novel clinical trial design, and how best to include children in the hoped-for benefits in targeted therapies.

We'd like to give special thanks to the Event Committee, especially event co-chairs Susan and Stephen Scherr and Lynn Bayard, and the many dedicated vendors and auction item donors for their generosity. We also thank the evening's sponsors: PhRMA, Biotechnology Innovation Organization, Fennec Pharmaceuticals, Juno Therapeutics, Novartis Oncology, and Pfizer Oncology.

Visit our blog to learn more about the Rosen Award and view photos of the beautiful evening, captured by Sarah Merians Photography.


Consider Designs that Donate in Your Holiday Shopping!

If you're searching for beautiful jewelry and accessories this holiday season, we suggest you check out Designs that Donate. They find unique items from designers around the world and then donate a percentage of your purchase total to the charity of your choice.

We're excited to be a featured charity for the month of December on Designs that Donate, and we hope you'll show your support by shopping their site! 

designsthatdonate.com


Check Your Year-End Giving Off Your List!

Yesterday was #GivingTuesday, and it marked the kick-off of our year-end giving campaign. We thank those of you who joined in the national movement to give back, after the flurry of Black Friday and Cyber Monday shopping.

Giving Tuesday may be over but the giving season has just begun. We are counting on your end-of-year generosity now more than ever, as we look ahead to the policy challenges facing children with cancer in 2017. (Bonus: If you check your year-end giving off your list today, we'll check you off our own list and spare you our December email appeals!)

Jessica Kean
September Bulletin: Awareness Month Highlights

September Awareness Month Showcases Strength of Advocate Community

This Childhood Cancer Awareness Month saw a series of events in Washington, DC that demonstrated the vitality and growing influence of the childhood cancer community.

Advocates pressed Congress on several bills that would improve treatment and care for kids with cancer - most notably the Childhood Cancer STAR Act, which we are pushing to pass before the end of the current legislative session. The White House buoyed our efforts with a proclamation and briefing on research projects by the National Cancer Institute and the President's Moonshot Initiative. [Read more in below section on the the Blue Ribbon Panel recommendations.]

The annual CureFest on September 18 brought childhood cancer organizations, including the Children's Cause, and hundreds of individual supporters to the National Mall for a show of solidarity and awareness. A full day of activities and stage performances was preceded by a candlelight vigil outside the White House the night before.

In other news, Hyundai Hope on Wheels, which has awarded $115 million to pediatric cancer research, hosted a scientific brainstorming conference and a gala for Hyundai business executives and families. Children's Cause President and Founder Susan Weiner spoke that evening about our advocacy initiatives.

To cap off a busy slate of events, Children's Cause was pleased to attend the 7th annual Childhood Cancer Summit, hosted by the Congressional Childhood Cancer Caucus. Advocates heard from NCI Director Doug Lowy about new developments in research, from Greg Simon - head of the President's Cancer Moonshot Initiative - about commitments to rapid improvements in treatment, and from patients and survivors on their challenges and victories.

September may be coming to a close but our advocacy and policy work continues year-round. Please help us send a louder message to policymakers that childhood cancer can no longer be ignored:

Donate now.


Pediatric Cancer Highlights from 'Moonshot' Report

The Children's Cause for Cancer Advocacy congratulates the National Cancer Moonshot Initiative - and specifically the Pediatric Cancer Working Group - on this month's release of ten cancer policy recommendations on research, clinical trials, data mining, prevention and patient engagement.

The panel's report, which was accepted by the National Cancer Advisory Board and the National Cancer Institute, was forward to a Moonshot Task Force headed by Vice President Biden and comprised of government representatives. The Task Force is scheduled to issue a report in October about proposed government initiatives relating to cancer. 

By design, the NCI Moonshot report focused on promising areas where progress is imminent. Of note to the Children's Cause are pediatric cancer recommendations around symptom management research, including survivorship, pediatric immunotherapy clinical trials, and oncoprotein research. Visit our blog for more details on these particular recommendations.

Children's Cause looks forward to working with the Moonshot Task Force and with Congress on the proposed recommendations with the hope and expectation that new targeted research improves the treatments for childrenwith cancer and maximizes survivors' well-being.


Landscape Report Reveals Gaps, Identifies Unique Barriers in Pediatric Cancer Research

A report on the current landscape of childhood cancer research was released this month by the Alliance for Childhood Cancer and the American Cancer Society, with guidance fromChildren's Cause. The report, "Translating Discovery into Cures for Children with Cancer," provides the latest information on trends, treatments, clinical trials, research funding and policy.

CCCA's president Susan Weiner sat on the report's 7-person Steering Committee to help develop this critical report. Highlights include: 

  • Inconsistent progress across cancer types, with a 40-50 percent 5-year survival rate for high-risk neuroblastoma, and DIPG remaining terminal.
  • Continuing high rates of late effects among childhood cancer survivors;
  • Barriers to pediatric cancer research and development of new therapies, including little incentive for companies and small patient populations for clinical trials.

You can read the one-page Executive Summary here (PDF).


In the News: Brain Tumors Now #1 Cause of Childhood Cancer Deaths

Because more children are now surviving leukemia than ever before, brain tumors have taken over as the leading cause of cancer deaths among children and adolescents. A new report from the National Center for Health Statistics paints an overall positive picture:childhood cancer death rates decreased by 20 percent from 1999 to 2014.

Today, 3 out of every 10 childhood cancer deaths are caused by brain cancer and one-quarter are from leukemia, the most common childhood cancer. These numbers are a reversal from 1999, when leukemia was the number one cancer killer among kids. In both 1999 and 2014, leukemia and brain cancer made up over half of all childhood cancer deaths.

It is important to emphasize that the survival rate for pediatric brain tumors has not increased -- nor has it significantly decreased over the years. A key takeaway from this report is the continued need for increased funding to learn more about all childhood cancers and the critical need for focused research to advance therapies for children with brain tumors.


New York Reception: November 3, 2016

You're invited to the Children's Cause for Cancer Advocacy's signature event of the year! Our annual reception and silent auction will take place at the James Burden Mansion in New York City from 7:00-9:30pm on November 3.

This year's event will feature William L. Carroll, MD, as our guest speaker. Dr. Carroll is the Director of Pediatric Hematology/Oncology at NYU Lagone's Hassenfeld Children's Center for Cancer and Blood Disorders. We will also be awarding the first annual Leonard M. Rosen Memorial Research Award at the event to Mary McCabe, RN, MA, Director of the Cancer Survivorship Initiative at Memorial Sloan-Kettering.

Tickets are now available!

If you have questions, contact Julie at jtaylor@childrenscause.org.

Jessica Kean