Sharing NAACCR Pediatric Cancer Initiatives on Dr. Rick Greene’s Cancer Registry World Podcast

hero_Association_1060x597-1

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

 

 

What to Read Next

Assessing the Completeness of Key Data Items Across NCCR Registries for Pediatric and Adult Cancer Cases

The National Childhood Cancer Registry (NCCR) was developed under the National Cancer Institute’s Childhood Cancer Data Initiative (CCDI)  to identify…

Your Voice Matters: Upcoming Public Comment Periods on US Health IT Standards

The U.S. Office of the National Coordinator for Health Information Technology (ONC) published two policy documents that will be of…

CiNA Statistics and CiNA*Explorer Update

In June 2024, the 2017-2021 CiNA cancer statistics were updated in CiNA*Explorer: https://apps.naaccr.org/explorer. This update reflects the final migration from…