Targeted Therapy in Pediatric AML: An Evolving Landscape

The outcomes associated with pediatric acute myeloid leukemia (AML) have improved over the last few decades, with the implementation of intensive chemotherapy, hematopoietic stem cell transplant, and improved supportive care. However, even with intensive therapy and the use of HSCT, both of which carry significant risks of short- and long-term side effects, approximately 30% of children are not able to be cured. The characterization of AML in pediatrics has evolved over time and it currently involves use of a variety of diagnostic tools, including flow cytometry and comprehensive genomic sequencing. Given the adverse effects of chemotherapy and the need for additional therapeutic options to improve outcomes in these patients, the genomic and molecular architecture is being utilized to inform selection of targeted therapies in pediatric AML. This review provides a summary of current, targeted therapy options in pediatric AML.

Automated summary

The treatment outcomes of pediatric acute myeloid leukemia have improved over the last few decades with the implementation of intensive chemotherapy and comprehensive genomic sequencing. However, despite the risks and side effects, a portion of patients are still unable to be cured. Advancements in genomic and molecular research are being utilized to develop targeted therapies for pediatric AML to improve outcomes.