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.
| ID | RF-NMZL-HIGH-RISK-BIOLOGY |
|---|---|
| Type | Red flag |
| Status | reviewed 2026-04-25 | pending_clinical_signoff |
| Diseases | DIS-NODAL-MZL |
| Sources | SRC-ESMO-MZL-2024 SRC-NCCN-BCELL-2025 |
Red Flag Origin
| Definition | TP53 mutation, NOTCH2 mutation (shared with SMZL), or aggressive histologic features — shorter PFS; favor R-CHOP or BR over rituximab monotherapy. |
|---|---|
| Clinical direction | intensify |
| Category | high-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.