The National Childhood Cancer Registry (NCCR) is a rapidly growing public health surveillance data resource. Its primary goal is to provide a platform to better understand the causes, outcomes, effective treatments, and later effects of cancer among children, adolescents, and young adults in the U.S. Developed under the NCI Childhood Cancer Data Initiative (CCDI), the NCCR contributes to the CCDI data ecosystem by serving as a linked infrastructure of central cancer registry data that will integrate various other childhood cancer data—from hospitals, research centers, heath care administrations, and other sources—to enhance access to and utilization of childhood cancer and survivorship data. The NCCR uses the Virtual Pooled Registry Cancer Linkage SystemExternal Web Site Policy to link multiple cancer registries and generate an accurate count of childhood cancer cases by combining information that appears in more than one registry.

Map of the 23 NCCR Registries
US map showing the locations of the 23 NCCR registries. The follow states and areas highlighted: NY, MA, CT, PA, NJ, OH, KY, TN, GA, FL, IL, IA, WI, LA, TX, NM, UT, ID, CA 
  	(including Greater Bay, Los Angeles), Seattle-Puget Sound, and HI.

The NCCR will be updated annually with newly diagnosed cases. NCCR plans to continuously expand its capacity through linkages to externally available data to enhance its database with genomic and tumor characteristics, longitudinal treatment information, indicators of cancer recurrence, and coexisting adverse health conditions.

The NCCR aims to serve the cancer surveillance and registry community, clinicians, researchers, policy makers, educators, and patients and their families by:

  • providing accurate counts and trends of childhood cancer incidence and survival,
  • supporting research on childhood cancer through potential sampling and data provision, and
  • enriching the value of rare and limited childhood cancer data through linkages and clinical applications.

Future Plans

The NCCR plans to expand the available statistics and is working on a Pediatric Cancer Explorer tool (Peds*Explorer), similar to SEER*Explorer, that will add more detail and flexibility to visualize incidence and survival statistics from the NCCR data. As new data are linked and made available, NCCR plans to release the updated data through various tools for cancer research.

In addition, the Centers for Disease Control and Prevention (CDC) and the National Cancer Institute have complementary initiatives to improve surveillance activities that inform our scientific understanding of pediatric cancer. Read more about plans to collaborate in the NCCR and STAR Overview: CDC and NCI Collaborate on Unique Initiatives for Pediatric Cancer Research (PDF, 182 KB).