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Aggressive HCC biology: macrovascular invasion (portal vein tumor thrombus segmental or m...

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

IDRF-HCC-HIGH-RISK-BIOLOGY
TypeRed flag
Statusreviewed 2026-04-26 | pending_clinical_signoff
DiseasesDIS-HCC
SourcesSRC-AASLD-HCC-2023 SRC-NCCN-HCC-2025

Red Flag Origin

DefinitionAggressive HCC biology: macrovascular invasion (portal vein tumor thrombus segmental or main), AFP >1000 ng/mL at baseline (high tumor burden marker), tumor doubling-time <3 months, OR poorly differentiated histology on biopsy. Predicts worse OS regardless of BCLC stage; favors more-active 1L choice (atezo+bev > sorafenib).
Clinical directionintensify
Categoryhigh-risk-biology

Trigger Logic

{
  "any_of": [
    {
      "finding": "portal_vein_tumor_thrombus",
      "value": true
    },
    {
      "comparator": ">=",
      "finding": "afp_baseline_ng_ml",
      "threshold": 1000
    },
    {
      "comparator": "<",
      "finding": "tumor_doubling_time_months",
      "threshold": 3
    },
    {
      "finding": "poorly_differentiated_histology",
      "value": true
    }
  ],
  "type": "composite_score"
}

Notes

IMbrave150 subgroup analysis: AFP >400 derives larger benefit from atezo+bev vs sorafenib (HR 0.55 vs 0.85 overall). Macrovascular invasion (Vp1-4) traditionally precluded surgical / loco-regional options, but doesn't preclude systemic ICI-combination.

Used By

No reverse references found in the YAML corpus.