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Mantle cell lymphoma with blastoid / pleomorphic morphology OR TP53 mutation OR del(17p)...

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

IDRF-MCL-BLASTOID-OR-TP53
TypeRed flag
Statusreviewed 2026-04-25 | pending_clinical_signoff
DiseasesDIS-MCL
SourcesSRC-ESMO-MCL-2024 SRC-NCCN-BCELL-2025

Red Flag Origin

DefinitionMantle cell lymphoma with blastoid / pleomorphic morphology OR TP53 mutation OR del(17p) — chemoimmuno-resistant aggressive variant; route directly to BTKi-based therapy
Clinical directionintensify
Categoryhigh-risk-biology
Shifts algorithmALGO-MCL-1L

Trigger Logic

{
  "any_of": [
    {
      "finding": "blastoid_morphology",
      "value": true
    },
    {
      "finding": "pleomorphic_morphology",
      "value": true
    },
    {
      "finding": "BIO-TP53-MUTATION",
      "value": "positive"
    },
    {
      "comparator": ">",
      "finding": "BIO-KI67-PROLIFERATION-INDEX",
      "threshold": 30
    },
    {
      "finding": "tp53_mutation",
      "value": true
    },
    {
      "finding": "del_17p",
      "value": true
    },
    {
      "finding": "ki67_above_30_percent",
      "value": true
    }
  ],
  "type": "composite_clinical"
}

Notes

Blastoid/pleomorphic + TP53-mutant MCL has poor response to chemoimmuno (BR/R-CHOP/R-DHAP) — survival impact substantial. Direct route to BTKi-based (acalabrutinib + rituximab; consolidation with allo-SCT or CAR-T at progression).

Used By

Algorithms

Biomarker

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