Acute leukemias

AMLALL
GeneticsProliferative: FLT3, JAK-2, C-KIT, ABL1
Inhibition of differentiation: RARA, NPM1
Epigenetic modulators: DNMT3A
NOTCH1, WT1, EZH2
t(12;21), t(9;22)
EpidemiologyOlder adultsChildren and older adults
Staging/classificationFAB (M0-M7)
WHO (I-VI)
FAB (L1-L3)
WHO (13 groups)
Additional informationAcute promyelocytic leukemia (APL) is a type of AML, WHO class I with t(15;17)
RA receptors are disrupted, promyelocytes accumulate with Auer rods (MPO aggregation; risk for DIC)
t(12;21) has a good prognosis, mostly seen in children

t(9;22) has a bad prognosis, mostly seen in adults (Philadelphia chromosome; BCR-ABL fusion)
TreatmentInduction: Cytarabine + anthracyclin (7+3)
Postinduction: Several doses of high-dose cytarabine
In FLT3 mutations: midostaurin
Anti-CD33










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