Table 1.

Major clinically relevant differences among ELN 2022, fifth edition of the WHO, and the ICC 2022 of myeloid neoplasms

ELN 2022 & ICC 2022WHO fifth edition
MDS/AML (without AML-defining genetic alterations) 10%-19% blasts Designated as MDS-IB2 (10%-19% bone marrow or 5%-19% peripheral blood or Auer rods) 
AML with antecedent MDS, MDS/MPN, or prior exposure to therapy Myelodysplasia added as a diagnostic qualifier Included as a separate entity, AML-MR 
AML with NPM1 mutations, KMT2A rearrangement, MECOM rearrangement, and NUP98 rearrangement Requires ≥10% blasts in bone marrow or peripheral blood Can be diagnosed irrespective of blast count 
AML with CEBPA mutation Requires ≥10% blasts in bone marrow or peripheral blood
Includes only bzip mutations 
Requires ≥20% blasts in bone marrow or peripheral blood
Includes biallelic and bzip mutations 
TP53 mutation Included separately in the hierarchical classification Not included as a separate entity for AML 
Therapy-related Added as a diagnostic qualifier Included as separate entity AML-pCT 
ELN 2022 & ICC 2022WHO fifth edition
MDS/AML (without AML-defining genetic alterations) 10%-19% blasts Designated as MDS-IB2 (10%-19% bone marrow or 5%-19% peripheral blood or Auer rods) 
AML with antecedent MDS, MDS/MPN, or prior exposure to therapy Myelodysplasia added as a diagnostic qualifier Included as a separate entity, AML-MR 
AML with NPM1 mutations, KMT2A rearrangement, MECOM rearrangement, and NUP98 rearrangement Requires ≥10% blasts in bone marrow or peripheral blood Can be diagnosed irrespective of blast count 
AML with CEBPA mutation Requires ≥10% blasts in bone marrow or peripheral blood
Includes only bzip mutations 
Requires ≥20% blasts in bone marrow or peripheral blood
Includes biallelic and bzip mutations 
TP53 mutation Included separately in the hierarchical classification Not included as a separate entity for AML 
Therapy-related Added as a diagnostic qualifier Included as separate entity AML-pCT 

bzip, basic leucine zipper; MDS, myelodysplasia; MDS-IB2, MDS with increased blasts; MPN, myeloproliferative neoplasm; pCT, post cytotoxic therapy.

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