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.
| ID | RF-HCC-HIGH-RISK-BIOLOGY |
|---|---|
| Type | Red flag |
| Status | reviewed 2026-04-26 | pending_clinical_signoff |
| Diseases | DIS-HCC |
| Sources | SRC-AASLD-HCC-2023 SRC-NCCN-HCC-2025 |
Red Flag Origin
| Definition | Aggressive 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 direction | intensify |
| Category | high-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.