The ALL-BFM registry has the primary goal of collecting population-based medical data from children and adolescents with ALL, regardless of participation in a clinical trial.
The collection and regular evaluation of the data is intended to contribute to ensuring the quality of structure, processes and results in the diagnosis and treatment of children with ALL in accordance with the guidelines for pediatric oncology (KiOn-RL). This also includes the possibility of analyzes for historical comparison with previous study populations or with ALL cohorts from other study groups.
The ALL-BFM registry has the primary goal of collecting population-based medical data from children and adolescents with ALL, regardless of participation in a clinical trial.
The collection and regular evaluation of the data is intended to contribute to ensuring the quality of structure, processes and results in the diagnosis and treatment of children with ALL in accordance with the guidelines for pediatric oncology (KiOn-RL). This also includes the possibility of analyzes for historical comparison with previous study populations or with ALL cohorts from other study groups.
