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MDS with TP53 mutation (mono- or biallelic) — distinct WHO 5th-ed entity with poor outcom...

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IDRF-MDS-TP53-MUTATION
TypeSignal d’alerte
Étatreviewed 2026-04-25 | pending_clinical_signoff
MaladiesDIS-MDS-HR DIS-MDS-LR
SourcesSRC-ESMO-MDS-2021 SRC-IPSS-M-BERNARD-2022 SRC-NCCN-AML-2025

Origine du drapeau rouge

DéfinitionMDS with TP53 mutation (mono- or biallelic) — distinct WHO 5th-ed entity with poor outcomes on HMA monotherapy and reduced alloHCT benefit; consideration of intensified / experimental therapy or palliative intent
Direction cliniqueintensifier
Catégoriehigh-risk-biology
Algorithme de décalageALGO-MDS-HR-1L

Logique de déclenchement

{
  "any_of": [
    {
      "finding": "tp53_mutation",
      "value": true
    },
    {
      "finding": "tp53_biallelic",
      "value": true
    },
    {
      "finding": "del_17p",
      "value": true
    },
    {
      "comparator": ">=",
      "finding": "tp53_vaf_pct",
      "threshold": 10
    }
  ],
  "type": "biomarker"
}

Notes

TP53-mutated MDS is its own WHO 5th-edition entity with median OS ~6-9 months on standard HMA. AlloHCT carries higher relapse risk vs TP53-wt. Active research questions: ven+aza vs aza alone, magrolimab + aza (failed phase-3 ENHANCE), eprenetapopt + aza (mixed results). NOT clear best regimen — flagged as intensify but the algorithm should also surface palliative-intent option. STUB — requires clinical co-lead signoff.

Utilisé par

Algorithmes

Biomarqueur

Indication

Signal d’alerte