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National Childhood Cancer Registry Explorer
CCDI
Data Resource:  CCDI
Point of Contact:  
NCIChildhoodCancerDataInitiative@mail.nih.gov,  
Registry

About This Dataset
NCCR*Explorer provides incidence, survival, and prevalence statistics for cancers in children and adolescent and young adults ages 0-39, using data from the National Childhood Cancer Registry (NCCR). It provides detailed statistics for a cancer site by sex, race/ethnicity, and age, and allows for comparison across cancer sites and subsites. Data from Cancer in North America (CiNA) (North American Association of Central Cancer Registries (NAACCR) 1995-2020 and the NCI's Surveillance, Epidemiology and End Results (SEER) Registries), submitted December 2022). Registries include: Arkansas, California (Greater Bay, Greater California, Los Angeles), Connecticut, Florida, Georgia, Hawaii, Idaho, Illinois, Iowa, Kentucky, Louisiana, Massachusetts, Michigan, New Jersey, New Mexico, New York, Ohio, Pennsylvania, Seattle (Puget Sound), Tennessee, Texas, Utah, Wisconsin. These 25 NCCR registries represent 70% of all U.S. children, adolescents, and young adults ages 0-39 based on 2020 U.S. Populations.
Core Data Elements
Number of Cases
1,897,938
Case Sex
Female (1,147,338); Male (750,600)
Case Age At Diagnosis
0 to 4 years (94,533); 5 to 9 years (55,044); 10 to 14 years (65,326); 15 to 19 years (109,125); 20 to 24 years (172,633); 25 to 29 years (280,848); 30 to 34 years (442,082); 34 to 39 years (678,347)
Case Race
American Indian or Alaska Native (9,929); Asian (99,099); Black or African American (212,970); White (1,529,479); Unknown (46,461)
Case Ethnicity
Hispanic or Latino (343,609); Not Hispanic or Latino (1,554,329)
Additional Data Elements
DATA REPOSITORY
Charts
Female (1,147,338); Male (750,600)
1,147,338Female