NCCR Fall Feature

By Fernanda Michels | November 3, 2025

The NCCR Fall Feature highlights key advancements and initiatives within the NCCR community, including highlights on the inaugural Data Jamboree, new study on clinical trial enrollment disparity using NCCR data, recent updates to NCCR*Explorer and SEER*Stat tools, and important upcoming deadline for NCCR registry participants Call for Data. Data Jamboree: Enhancing Childhood Cancer Data Sharing…

CBTRUS and Cancer Registries: 35 Years of Collaboration

By Carol Kruchko | October 27, 2025

We couldn’t have done it without you! This sums up our relationship with the surveillance community, its stakeholders, and its supporting community. For over 35 years, the Central Brain Tumor Registry of the United States (CBTRUS) has worked with you to quantify the burden of brain and other central nervous system (CNS) tumors on the…

Nominations Opening Soon for the 2026-2027 Board of Directors

By Lucinda Ham, RHIA, ODS-C | October 20, 2025

The Nominating Committee is seeking nominees to run for election to three key leadership roles on the NAACCR Board of Directors, with terms beginning June 2026, as well as candidates for the 2026-2027 Nominating Committee. The NAACCR membership will cast ballots for the following positions: President-Elect. Four-year commitment: one year as President-Elect, two years as…

Using Median/Multiple Outlier Testing (MMOT) to Support Central Cancer Registry Operations

By Fernanda Michels | August 3, 2026

Central Cancer Registries continuously strive to improve data quality while ensuring that data are fit for research, surveillance, and cancer control activities. One promising approach is the use of Median/Multiple Outlier Testing (MMOT), a benchmarking method developed by Dr. Huann-Sheng Chen of the National Cancer Institute’s Surveillance Research Program. MMOT helps identify unusual patterns in…

National Childhood Cancer Registry Summer Feature

By Fernanda Michels | July 27, 2026

The NCCR Summer Feature shares the highlights from the National Childhood Cancer Registry (NCCR) session held at the 2026 NAACCR Annual Conference. This edition also features funding opportunities, new data source included in the NCCR Data Platform upcoming CCDI symposium, and the 2026 NCI Data Jamboree. Highlights of the 2026 NAACCR Annual Conference The 2026…

Exploring New Approaches to Data Collection: Modular Records Task Force Final Report

By Ashley Harvieux | July 20, 2026

The Modular Records Task Force was initiated in August 2025 to support the NAACCR Board’s Strategic Plan on the strategic initiative for Innovative Approaches to Data Collection (Minimal Datasets and Partial Records): Improving timeliness through innovative approaches to data collection. The purpose of the task force was to define a new “modular” approach to cancer…

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OUR MISSION

Actionable content that unites cancer registries.

The Narrative strives to provide you with information you can use to enhance and strengthen your cancer registry. Look to the Narrative for the latest cancer surveillance news, trends, advances in technology, and latest educational opportunities.

OUR VISION

Make every cancer count.

Cancer affects thousands of people across North America every year. Each cancer case must contribute to our knowledge and understanding so that we may reduce the burden of these diseases. Narrative provides a platform for the cancer surveillance community to collaborate and share data that will improve health outcomes.

CANCER REGISTRY SPOTLIGHT: MICHIGAN

Successful Linkage Between Registry Database and LexisNexis

In our ongoing commitment to enhance the quality and accessibility of data, we are thrilled to announce the successful linkage between our registry database and LexisNexis. This integration represents a significant step forward in streamlining our data processes and expanding our analytical capabilities.