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ELN 2022 Risk (AML)

Haematological Malignancies

Favorable, intermediate, or adverse AML risk assignment using ELN 2022 genetics.

Calculated Interpretation

Intermediate Risk

Intermediate risk includes FLT3-ITD without adverse lesions and non-favorable/non-adverse profiles.

EVIDENCE SYNTHESIS

Clinical Reference Hub

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

CLINICAL INSIGHT

When to Use

Primary Use

  • Favorable, intermediate, or adverse AML risk assignment using ELN 2022 genetics.
CLINICAL INSIGHT

How it Works

Clinical Inputs

Core-binding factor fusion
NPM1 mutation
In-frame bZIP CEBPA mutation
TP53 mutation
Myelodysplasia-related gene mutation
Adverse cytogenetics
KMT2A rearrangement
RUNX1 mutation
ASXL1 mutation
BCOR mutation

Interpretive Logic

  • Adverse lesions override favorable markers.
  • FLT3-ITD without adverse lesions now sits in intermediate risk regardless of allelic ratio.
  • Core binding factor, mutated NPM1, and bZIP CEBPA patterns remain favorable.
CLINICAL INSIGHT

Practical Pearls

Result Bands

Favorable
Intermediate
Adverse
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

Favorable, intermediate, or adverse AML risk assignment using ELN 2022 genetics.

OpiCalc Medical Oncology ModuleHaematological Malignancies2026
CLINICAL INSIGHT

Background

Context

ELN 2022 Risk (AML) is included in the oncology module as a structured decision-support tool for haematological malignancies workflows.

No clinical reference data available.