Recommendations for Diagnosis and Treatment of Children with Transient Abnormal Myelopoiesis (TAM) and Myeloid Leukemia in Down Syndrome (ML-DS).
Sina Al-KershiRichard GolnikMarius FlasinskiKatharina WaackMareike RascheUrsula CreutzigMichael DworzakDirk ReinhardtJan-Henning KlusmannPublished in: Klinische Padiatrie (2021)
Children with Down syndrome are at a high risk of developing transient abnormal myelopoiesis (TAM; synonym: TMD) or myeloid leukemia (ML-DS). While most patients with TAM are asymptomatic and go into spontaneous remission without a need for therapy, around 20% of patients die within the first six months due to TAM-related complications. Another 20-30% of patients progress from TAM to ML-DS. ML-DS patients are particularly vulnerable to therapy-associated toxicity, but the prognosis of relapsed ML-DS is extremely poor - thus, ML-DS therapy schemata must strive for a balance between appropriate efficacy (to avoid relapses) and treatment-related toxicity. This guideline presents diagnostic and therapeutic strategies for TAM and ML-DS based on the experience and results of previous clinical studies from the BFM working group, which have helped reduce the risk of early death in symptomatic TAM patients using low-dose cytarabine, and which have achieved excellent cure rates for ML-DS using intensity-reduced treatment protocols.
Keyphrases
- end stage renal disease
- ejection fraction
- acute myeloid leukemia
- low dose
- chronic kidney disease
- newly diagnosed
- peritoneal dialysis
- bone marrow
- prognostic factors
- oxidative stress
- young adults
- stem cells
- systemic lupus erythematosus
- dendritic cells
- high dose
- immune response
- risk factors
- patient reported
- patient reported outcomes
- diffuse large b cell lymphoma
- high intensity
- blood brain barrier
- replacement therapy
- ulcerative colitis