Description of Collaborative Activity: |
The NCCR has been established by relying on a core of registry data from 1995 forward for all cancers diagnosed in children aged 0-19. NCI SEER and CDC NPCR registries are submitting population-based registry data and this is linked with a variety of other data sources (e.g., claims, molecular characterization, pharmacy, Virtual Pooled Registry, research studies, SDoH, Cancer Center supplements) to obtain a longitudinal understanding of treatment, procedures, risk factors, and outcomes. |
