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TP53 mutation, NOTCH2 mutation (shared with SMZL), or aggressive histologic features — sh...

Deterministic view of the source YAML entity. Clinical authority remains with the cited source IDs and reviewer sign-off state.

IDRF-NMZL-HIGH-RISK-BIOLOGY
TypeRed flag
Statusreviewed 2026-04-25 | pending_clinical_signoff
DiseasesDIS-NODAL-MZL
SourcesSRC-ESMO-MZL-2024 SRC-NCCN-BCELL-2025

Red Flag Origin

DefinitionTP53 mutation, NOTCH2 mutation (shared with SMZL), or aggressive histologic features — shorter PFS; favor R-CHOP or BR over rituximab monotherapy.
Clinical directionintensify
Categoryhigh-risk-biology

Trigger Logic

{
  "any_of": [
    {
      "finding": "tp53_mutation",
      "value": true
    },
    {
      "finding": "notch2_mutation",
      "value": true
    }
  ],
  "type": "biomarker"
}

Notes

NMZL molecular landscape overlaps SMZL; adverse markers warrant combination chemoimmuno. Indication-level decision.

Used By

No reverse references found in the YAML corpus.