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Case-based visualization of a patient cohort using SEER epidemiologic data.
Christian Maier1, Thomas Bürkle1, Hans-Ulrich Prokosch1
1Friedrich-Alexander-University Erlangen/Nuernberg.
Integrating the Surveillance, Epidemiology and End Results (SEER) cancer registry with electronic health records offers potential for clinical decision-making. However, missing data elements like receptor status limit its current utility in patient care.
Area of Science:
- Oncology
- Public Health
- Health Informatics
Background:
- Cancer registry data are crucial for epidemiological tracking and informing clinical decisions.
- Limited integration exists between public cancer datasets and electronic patient records for clinical use.
- Electronic patient records lack direct access to comprehensive cancer registry information.
Purpose of the Study:
- To implement a proof-of-concept integration of the SEER (Surveillance, Epidemiology and End Results) dataset with a digital breast cancer tumor board.
- To evaluate the utility of this integration within a German university hospital's clinical setting.
- To explore dynamic data visualization for cohort composition and survival analysis.
Main Methods:
- Integration of the public SEER dataset with a digital breast cancer tumor board system.
- Utilizing routine documentation for data input and dynamic visualization.
- Generating cohort composition and Kaplan-Meier survival plots.
- Conducting an evaluation of the implemented system.
Main Results:
- Successful proof-of-concept integration was established.
- Dynamic visualizations of cohort composition and survival plots were generated.
- Favorable feedback was received on the concept and implementation.
- Key data elements, such as receptor status, were identified as missing in the SEER dataset, limiting clinical utility.
Conclusions:
- The integration of SEER data into clinical workflows is feasible and conceptually valuable.
- The current SEER dataset's limitations, particularly missing crucial clinical data, restrict its direct application in individual patient diagnostic and treatment decisions.
- Further development is needed to enhance the completeness of registry data for improved clinical utility.
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