Acute myeloid leukemia
ICD-10 C92.0 · ICD-11 2A60

Consolidation Treatment for ELN Favourable or Intermediate Risk AML After Achieving CR/CRi with Second Induction

This protocol addresses adults with acute myeloid leukaemia classified as ELN favourable or intermediate risk who have achieved complete remission (CR) or CR with incomplete haematological recovery (CRi) following a second induction cycle — and who do not have core binding factor AML, therapy-related AML, AML with myelodysplasia-related changes, FLT3-ITD/TKD-positive disease, or ELN adverse-risk features.

Clinical Scenario

ELN favourable or intermediate risk AML, specifically excluding: core binding factor AML, therapy-related AML, AML with myelodysplasia-related changes, FLT3-ITD/TKD-positive disease, and ELN adverse-risk classification. In patients where none of these markers is present, standard induction chemotherapy is the initial approach.

Preceding Treatment Step

The prior step was a second induction cycle — either repeating the initial induction regimen or a regimen incorporating intermediate-dose cytarabine (IDAC), such as FLAG-Ida. The aim was to achieve CR/CRi (fewer than 5% blasts in the bone marrow). Having reached that remission milestone, this consolidation protocol defines the next phase of management.

Consolidation Approach (Partial Overview)

Post-remission management for these patients involves either chemotherapy consolidation or haematopoietic cell transplantation. The appropriate pathway differs by ELN risk group and by individual patient factors. The complete algorithm — including risk-stratified sequencing and eligibility considerations — is in the full protocol.

Instant Access to Structured Evidence-Based Regimens
References
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