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Updated: Jul 24, 2026
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Generation of Comprehensive Thoracic Oncology Database - Tool for Translational Research
Published on: January 22, 2011
Panel discussion. Data needs in cancer
W T McGivney1, M L Barker, J E Bost
1National Comprehensive Cancer Network, Rockledge, Pennsylvania, USA.
Oncology (Williston Park, N.Y.)
|February 24, 1999
Summary
The National Comprehensive Cancer Network (NCCN) has launched a comprehensive cancer outcomes database to track patient care and outcomes. This initiative aims to improve quality improvement programs and support clinical research across NCCN sites.
Area of Science:
- Oncology
- Health Services Research
- Data Science
Background:
- The National Comprehensive Cancer Network (NCCN) developed a prospective, comprehensive outcomes database.
- This initiative followed a 2-year study to test data collection methods and systems.
- The database initially focused on 400 newly diagnosed breast cancer patients at five NCCN sites.
Purpose of the Study:
- To establish capabilities for analyzing and reporting cancer care patterns and outcomes.
- To enable NCCN members to assess guideline compliance and benchmark performance.
- To support clinical research, quality improvement, and healthcare partnerships.
Main Methods:
- Prospective data collection from NCCN sites.
- Expansion to include over 12,000 patients with common cancers within 3 years.
- Collaboration with healthcare partners to define data needs.
Main Results:
- The database is designed to facilitate the analysis of cancer care patterns and outcomes.
- It will enable performance benchmarking against NCCN clinical practice guidelines.
- The project aims to foster a continuous quality improvement program.
Conclusions:
- The comprehensive outcomes database is a key initiative for the NCCN.
- It is expected to enhance quality of care, support research, and facilitate collaborations.
- The database will provide valuable insights into cancer treatment patterns and patient outcomes.
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