What are the two main types of data collected by tumor registries?

Tumor registries primarily focus on collecting comprehensive information related to cancer occurrences and their management. The two main types of data they collect are demographic data and clinical data.

Demographic data includes vital statistics about the patients, such as age, gender, race, and geographic location. This information is essential for understanding the epidemiology of cancer and identifying at-risk populations. It allows researchers and public health officials to evaluate cancer trends and disparities across different demographics.

Clinical data encompasses details regarding the diagnosis, treatment, and outcomes of cancer. This includes information about tumor characteristics, staging, treatment protocols, and follow-up results. Clinical data is crucial for assessing the quality of care, effectiveness of treatments, and overall survival rates.

By focusing on these two categories, tumor registries can effectively compile a comprehensive dataset that supports cancer research, treatment optimization, and public health initiatives.