During this webinar, presenters from IMS and NAACCR will review and discuss updates to… 1. On-line submission procedures and forms 2. New data items, Updates to Data Assurance Agreement & Consent Forms 3. NAACCRPrep 4. Call for Data Edits 5. Other CFD tasks (Virtual Pooled Registry file submission, CaRRI, registry contact updates) The webinar will be recorded and posted to the NAACCR Call for Data page after the webinar: https://www.naaccr.org/call-for-data/ Submission documents will be posted by Thursday, September 13th. Additional tools and supplemental information will be posted as soon as available. We strongly encourage anyone involved in the NAACCR Call for Data submission to view this webinar.

During this webinar, presenters will introduce, review, demo and/or discuss: 1. Alias Tables for improving data quality and reducing the burden of manual matches 2. Micro Match Status-a new variable describing the quality of a geocoding match 3. Advanced Search options including "Exhaustive Search," "Uncertainty Hierarchy," and "Limit Minimum Match Score" 4. New NAACCR Manual Geocoding Interface (Beta version) 5. Operations: how to interpret long/lat precision, which census years to append This webinar is relevant to all users of the NAACCR Geocoder including those accessing via the NAACCR Webpage or API, such as SEER*DMS users.

This webinar aims to more broadly share information on the Virtual Pooled Registry Cancer Linkage System (VPR-CLS) that was presented during the 2019 NAACCR/IACR Annual Meeting. Geared toward U.S. registries with knowledge of the VPR-CLS, the webinar will include presentations on the following: - VPR-CLS Pilot Testing and Next Steps - Status of the Templated IRB/Registry Application, Implementation of the Central IRB, and Local Context Issues - Cancer Ascertainment by U.S. Population-Based Cancer Registries, Self-Report and Death Certificates in the Nationwide U.S. Radiologic Technologist Cohort: A Preliminary Report

On behalf of NAACCR and our co-authors from ACS, CDC, and NCI, we are pleased to present a webinar on the latest Annual Report to the Nation on the Status of Cancer. This is our 21st Annual Report, and NAACCR was the lead agency. The Annual Report represents a collaborative effort by senior researchers from each major cancer surveillance organization in the United States to produce the up to date and comprehensive trends in cancer incidence and mortality. Each year we also focus on a special topic, and this year we focused on cancer among adults aged 20-49.

California is the most populated state and has the largest ethnic/racial minority population in the US. With 20% of the nation’s minority population living in the state, California has a unique population to both describe and serve in regards to cancer prevention and control. This NAACCR Talk highlights three California, minority-focused cancer research projects on Chinese Americans, Hispanics, and African Americans.

The Surveillance Research Program (SRP) at the Division of Cancer Control and Population Sciences of the National Cancer Institute provides national leadership in the science of cancer surveillance in the US, which includes analytical tools and methodological expertise in collecting, analyzing, interpreting, and disseminating reliable population-based cancer statistics. This surveillance infrastructure benefits the public, policymakers, and scientists in understanding changes in cancer incidence and outcomes in all segments of the US population over time. The objective of the webinar is to provide an overview of the breadth and scope of statistical software and tools in the areas of incidence and mortality, survival, prevalence, and geospatial methods and tools. At the completion of the webinar, audience will gain a basic understanding of the software/tools and will be able to explore in more details into specific tools that are applicable in their own work.

Starting in 2020, after nearly 30 years of defining a fixed width format for data exchange, NAACCR will be transitioning Volume II of the NAACCR Data Standards and Data Dictionary to an XML based format. This webinar will highlight the readiness of registry software vendors for this important new data standard, as well as explaining the rich set of software resources and technical expertise available to the NAACCR community to make sure this transition to XML is as seamless as possible. This webinar will include presentations from NPCR, SEER, and the NAACCR XML Data Exchange Workgroup. If you are interested in the impact that NAACCR XML will have on your registry or organization and you would like to know the latest news on the XML transition, be sure to attend this webinar.

SEER*Stat is a powerful statistical application that is available free of charge from the US National Cancer Institute and provides a mechanism for the analysis of population-based cancer registry data. It has modules for the analysis and reporting of the four most common cancer-related metrics: incidence, survival, prevalence, and mortality.

SEER*Stat is a powerful statistical application that is available free of charge from the US National Cancer Institute and provides a mechanism for the analysis of population-based cancer registry data. It has modules for the analysis and reporting of the four most common cancer-related metrics: incidence, survival, prevalence, and mortality.

During the 2017 Louisiana Legislative Session, a new law was signed requiring that the Louisiana Tumor Registry (LTR) produce and release cancer incidence counts and rates at the census tract level. Previously, cancer statistics could be released to the public at the parish (county) level. To comply with this law, the LTR convened a team, including experts from NCI-SEER and IMS, to develop the appropriate methodology to produce incidence rates at the census tract level while ensuring rate stability and patient confidentiality. The objective of this presentation is to describe the LTR's experience with identifying the appropriate population source, selecting the time period for the analysis, and producing reliable cancer statistics at the census tract level, as well as to share a summary of the results.