Turn your cancer data into better decisions. NCDB Reporting Tools give CoC-accredited cancer programs actionable insights to evaluate care, benchmark performance, strengthen data quality, and identify opportunities for improvement.
The National Cancer Database (NCDB) provides Commission on Cancer (CoC)-accredited programs with reporting tools to monitor patient outcomes, assess quality, benchmark performance, improve data accuracy, and support accreditation.
Using data submitted through the Rapid Cancer Reporting System (RCRS), NCDB reports provide insight into patient demographics, staging, treatment, outcomes, and quality measure performance—helping cancer programs understand their performance and identify opportunities for improvement.
Primary Use
Monitor compliance with CoC evidence-based quality measures and identify cases requiring review or quality improvement.
Data Included
Case eligibility, concordance status, estimated performance rates (EPR), numerator/denominator counts, treatment summaries, and benchmark statu
Primary Use
Identify patients approaching or exceeding treatment timelines to improve timeliness of care and support quality measure compliance.
Data Included
Cases approaching or exceeding treatment timelines for selected Quality Measures, plus applicable edit errors.
Primary Use
Evaluate long-term patient outcomes and compare survival across patient groups.
Data Included
Overall observed survival by cancer site, stage, sex, age, and comorbidity.
Primary Use
Use an annual executive-level summary to benchmark performance and identify quality improvement priorities.
Data Included
Annual PowerPoint summary combining Hospital Comparison, Survival, RCRS quality measures, operative mortality, and risk-adjusted survival.
Primary Use
Benchmark clinical practice, treatment patterns, timeliness, and disparities against CoC state, regional, and national programs.
Data Included
Patient demographics, stage distribution, tumor characteristics, treatments, and Days-to-Treatment metrics compared with CoC state, regional, and national program benchmarks including complete data submitted within the prior month.
Primary Use
Compare quality measure performance across facilities, states, regions, ACS Divisions, program categories, and CoC programs.
Data Included
Quality measure performance compared with CoC facility, state, region, ACS Division, program category, or all CoC programs, with demographic stratification.
Primary Use
Identify missing, unknown, or incomplete registry data to improve data quality.
Data Included
Registry data fields with missing, unknown, or incomplete values compared with national five-year averages within RCRS.
Primary Use
Track monthly submissions, edit-free rates, and timeliness to support RCRS reporting requirements.
Data Included
Monthly case upload status, percentage of edit-free submissions, diagnosis year progress, primary site counts, and submission timeliness for complete analytic cancer cases submitted to RCRS
Primary Use
Monitor submission status, registry errors, duplicate records, and data submitted to RCRS.
Data Included
Complete and incomplete RCRS submitted cases, diagnosis year, primary site, submission history, edit errors, duplicate cases, and case details.
Primary Use
Access HIPAA-compliant, de-identified patient-level NCDB data for research, outcomes analysis, and quality improvement.
Data Included
HIPAA-compliant, de-identified patient-level NCDB research dataset.