Targeted Therapy in Pediatric AML: An Evolving Landscape.
LaQuita M JonesKatherine TarlockTodd M CooperPublished in: Paediatric drugs (2021)
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.
Keyphrases
- acute myeloid leukemia
- allogeneic hematopoietic stem cell transplantation
- hematopoietic stem cell
- flow cytometry
- healthcare
- end stage renal disease
- ejection fraction
- emergency department
- single cell
- quality improvement
- newly diagnosed
- locally advanced
- palliative care
- acute lymphoblastic leukemia
- copy number
- squamous cell carcinoma
- adipose tissue
- stem cells
- peritoneal dialysis
- patient reported outcomes
- mesenchymal stem cells
- risk assessment
- prognostic factors
- metabolic syndrome
- human health
- bone marrow
- adverse drug
- health insurance