Research and Training Programs

Clinical and genetic risk factors associated with adverse long-term health outcomes after curative therapies in individuals with sickle cell disease

The primary objective is to implement a personalized approach to curative therapies for children and adults with sickle cell disease (SCD) to maximize benefits while minimizing adverse outcomes. Current efforts to understand long-term health outcomes after these therapies are limited. The focus on initial treatment success recalls developments in pediatric oncology during the 1980s, where effective therapies eventually led to increased risks of organ dysfunction and malignancies.