WHO 2016: CLASSIFICATION OF HIGH-RISK AML SUBTYPES: t-AML AND AML-MRC

THERAPY-RELATED AML (T-AML)

According to WHO, t-AML is defined as previously untreated AML with a history of prior cytotoxic therapy1,2*

Cytotoxic therapies associated with development of t-AML2 :

  1. Alkylating agents and radiation
    1. Latency period of 4–10 years
  2. Topoisomerase II inhibitors
    1. Latency period of 2–3 years
  3. Immunosuppressive therapies
    1. Latency period of 3–4 years

AML, WITH MYELODYSPLASIA-RELATED CHANGES (AML-MRC)

AML: ≥20% blasts in peripheral blood2

AML arising from a prior MDS or an MDS/MPN2

OR

AML with an MDS-related cytogenetic abnormality2

OR

AML with multilineage dysplasia2

A diagnosis of AML-MRC may require cytogenetic testing or a morphology exam for confirmation1

aml-history
aml-history

The classification of AML has been updated to reflect breakthroughs in disease understanding1,3,4

  • The VYXEOS indication is based on the WHO 2016 classification of AML1
  • The 2022 WHO and ICC classifications have revised the definition of AML-MRC and t-AML3,4
classification-en-desk
classification-en-mob

Myelodysplasia-related cytogenetic abnormalities as described in the WHO 2022 and ICC 2022 Guidelines

The WHO 2022 and ICC classifications share overlapping cytogenetic abnormalities

who-classification
who classification
CA-VYX-2400006-E | March 2024