ESR1 ligand-binding-domain hotspot Y537S or D538G — the two dominant hotspots (~70% of al...
Детермінований перегляд YAML-сутності з джерельної бази. Клінічний авторитет лишається за вказаними source ID та статусом клінічного sign-off.
| ID | RF-BREAST-ESR1-Y537S-D538G-CANDIDATE |
|---|---|
| Тип | Тривожна ознака |
| Статус | переглянуто 2026-04-29 |
| Хвороби | DIS-BREAST |
| Джерела | SRC-EMERALD-BIDARD-2022 SRC-ESMO-BREAST-METASTATIC-2024 SRC-NCCN-BREAST-2025 |
Походження тривожної ознаки
| Визначення | ESR1 ligand-binding-domain hotspot Y537S or D538G — the two dominant hotspots (~70% of all ESR1-LBD mutations) acquired in HR+/HER2- metastatic breast progressing on aromatase inhibitor. EMERALD (Bidard 2022) randomized post-AI ± CDK4/6i HR+ MBC to elacestrant vs endocrine standard-of-care; PFS benefit was concentrated in the ESR1-mutant subgroup (mPFS 3.8 vs 1.9 mo, HR 0.55). Y537S is associated with more aggressive biology than D538G in some series. Candidate RF refines RF-BREAST-ESR1-MUT-ACTIONABLE for the predominant hotspots specifically targeted by elacestrant data. |
|---|---|
| Клінічний напрям | intensify |
| Категорія | high-risk-biology |
Логіка спрацьовування
{
"any_of": [
{
"finding": "esr1_y537s",
"value": true
},
{
"finding": "esr1_d538g",
"value": true
},
{
"finding": "esr1_hotspot",
"value": "Y537S"
},
{
"finding": "esr1_hotspot",
"value": "D538G"
},
{
"finding": "esr1_mutation",
"value": "Y537S"
},
{
"finding": "esr1_mutation",
"value": "D538G"
}
],
"type": "biomarker"
}
Нотатки
Hotspot-specific narrowing of RF-BREAST-ESR1-MUT-ACTIONABLE. Y537S + D538G together account for ~70% of LBD mutations and are the hotspots most consistently represented in EMERALD subgroup analyses. Test on ctDNA at progression on AI ± CDK4/6i — preferred specimen due to subclonal + polyclonal nature of ESR1 mutations in tissue. Priority 67 sits between the broad ESR1-MUT-ACTIONABLE (70) and the AKT/PIK3CA family (65) — the engine should fire both this hotspot RF and the broader ESR1 RF when applicable; conflict resolution defers to clinical_direction (both intensify, no conflict). When ESR1-WT post-AI: elacestrant did not show benefit; switch to fulvestrant + capivasertib / alpelisib if PIK3CA / AKT1 / PTEN altered. EMERALD trial Source ingested (SRC-EMERALD-BIDARD-2022).
Де використовується
Indications
IND-BREAST-HR-POS-MAINT-CDK46I- IND-BREAST-HR-POS-MAINT-CDK46IIND-BREAST-HR-POS-MET-1L-CDKI- IND-BREAST-HR-POS-MET-1L-CDKI