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WHO 2022 / ICC 2022 AML

Haematological Malignancies

Molecularly defined AML classification using key defining rearrangements and mutations.

Calculated Interpretation

AML, NOS / requires integrated morphologic review

WHO 2022 / ICC 2022 classification is driven by defining molecular and cytogenetic lesions.

EVIDENCE SYNTHESIS

Clinical Reference Hub

Curated insights • How it Works • Practical Pearls • Evidence Base

CLINICAL INSIGHT

When to Use

Primary Use

  • Molecularly defined AML classification using key defining rearrangements and mutations.
CLINICAL INSIGHT

How it Works

Clinical Inputs

PML::RARA
RUNX1::RUNX1T1
CBFB::MYH11
KMT2A rearrangement
DEK::NUP214
BCR::ABL1
NPM1 mutation
In-frame bZIP CEBPA mutation
TP53 mutation
Myelodysplasia-related gene mutation
Myelodysplasia-related cytogenetics

Interpretive Logic

  • Defining fusions and canonical mutations override morphology-only buckets.
  • Myelodysplasia-related AML is recognized by defining cytogenetic or gene features.
  • TP53-mutated AML is treated as a distinct high-risk biologic group.
CLINICAL INSIGHT

Practical Pearls

Result Bands

Fusion-defined AML
Mutation-defined AML
MR-AML
CLINICAL INSIGHT

Next Steps

Suggested Next Steps

  • Interpret the result in the full disease-specific clinical context.
  • Correlate with pathology, imaging, performance status, and multidisciplinary guidance.
CLINICAL INSIGHT

Evidence Base

Evidence Base

Molecularly defined AML classification using key defining rearrangements and mutations.

OpiCalc Medical Oncology ModuleHaematological Malignancies2026
CLINICAL INSIGHT

Background

Context

WHO 2022 / ICC 2022 AML is included in the oncology module as a structured decision-support tool for haematological malignancies workflows.

No clinical reference data available.