Summary
Abstract Allogeneic hematopoietic stem cell transplantation (HSCT) is the only curative treatment for patients with high- risk acute myeloid leukemia (AML). However, HSCT is affected by graft-versus-host disease (GvHD) and graft- versus-leukemia (GvL) effects, both are mediated by donor T lymphocytes and significantly impact treatment success and thus overall outcome. AML patients commonly harbor FLT3/internal tandem duplication (FLT3-ITD), a mutation in the receptor tyrosine kinase FLT3 that is associated with poor prognosis. FLT3 targeted therapies have proven clinical benefit particularly w
