What is a key feature of the pediatric registry compared to others?

A key feature of a pediatric registry is its focus on a specific population, which typically includes patients from birth up to 18 years of age, and sometimes extends to young adults up to age 30. This distinguishes it from other cancer registries that may encompass a broader age range, including both children and adults.

The pediatric registry is designed to capture data specific to childhood cancers, which often have different etiologies, treatment responses, and outcomes compared to cancers that typically affect adults. By occasionally including cases up to age 30, the pediatric registry can also monitor transition periods where young adults may still be affected by conditions typically classified under pediatric oncology, allowing for a more comprehensive understanding of cancer trends in younger populations. This focus on a defined age group is crucial for developing age-appropriate treatment protocols and addressing the unique needs of younger patients.