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AML with FLT3-ITD or FLT3-TKD mutation — addition of midostaurin (or gilteritinib in r/r)...

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IDRF-AML-FLT3-ACTIONABLE
TipoSinal de alerta
Estadoreviewed 2026-04-25 | pending_clinical_signoff
DoençasDIS-AML
FontesSRC-ELN-AML-2022 SRC-NCCN-AML-2025 SRC-RATIFY-STONE-2017

Origem da bandeira vermelha

DefiniçãoAML with FLT3-ITD or FLT3-TKD mutation — addition of midostaurin (or gilteritinib in r/r) to induction is required (RATIFY trial)
Direcção clínicaintensificar
Categoriahigh-risk-biology
Algoritmo de deslocamentosALGO-AML-1L

Lógica de Desencadeamento

{
  "any_of": [
    {
      "finding": "flt3_itd",
      "value": true
    },
    {
      "finding": "flt3_tkd",
      "value": true
    },
    {
      "finding": "flt3_mutation",
      "value": "positive"
    }
  ],
  "type": "biomarker"
}

Notas

Triggers addition of midostaurin 50 mg PO BID days 8-21 to 7+3 induction + HiDAC consolidation in fit patients. Gilteritinib is the r/r-AML standard. NOT applicable for unfit patients on ven+aza (FLT3-targeting in that setting under investigation; not yet standard). Access: midostaurin not Ukraine-reimbursed — major barrier. STUB — requires clinical co-lead signoff.

Usado por

Algoritmos

Indicação

Sinal de alerta