Sharing NAACCR Pediatric Cancer Initiatives on Dr. Rick Greene’s Cancer Registry World Podcast
I am excited to share that I was recently interviewed by Dr. Rick Greene for his Cancer Registry World podcast.
It was a great opportunity to share my path into cancer surveillance and to highlight the pediatric work we are advancing through NAACCR. In the episode, I discussed several initiatives within the National Childhood Cancer Registry (NCCR), including our efforts to evaluate and enhance data quality and to support the NCCR data products, including the Data Platform.
I also talked about the incredible progress being made by NAACCR’s Pediatric SSDI Work Group, especially around developing the Pediatric Staging Manual and preparing registrars and selected hospitals for the rollout of the Pediatric Data Collection System.
This conversation offers a meaningful look at NAACCR’s commitment to advancing the quality and usefulness of cancer registry data to reduce the impact of cancer on children and their families.
You can listen to my conversation with Dr. Greene here: https://open.spotify.com/episode/6JPuLiBM4sMxAux0Jpl6Re
Tags: Childhood Cancer, Featured, NCCR, PDCS, Pediatric SSDI WG, Podcast
What to Read Next
Now Is the Time to Champion Cancer Registries: Help Spread the Word
Recent events have made it clear: we must do more to elevate the visibility and importance of cancer surveillance. In…
Reflections on the 2025 Annual Conference
Karen Knight, Executive Director of NAACCR, shares her reflections from the conference, with a call to leadership and working together…
What’s new for v26?
Changes to data collection standards, registry operations, and cancer registry software products impact hospital registrars, central registries, standard setting agencies,…


