Onco Wiki / Maladie

Sarcome épithélioïde

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IDDIS-EPITHELIOID-SARCOMA
TypeMaladie
Alias
EStype distal de sarcome épithélioïdesarcome épithélioïd proximal typeЕпітеліоїдна саркома
Étatreviewed 2026-05-04 | pending_clinical_signoff
MaladiesAucune déclaration
SourcesSRC-ESMO-SARCOMA-2024 SRC-EZH202-GOUNDER-2020 SRC-NCCN-SARCOMA

Informational support. All recommendations must be verified by a qualified oncologist. Engineering checks are not clinical validation or treatment approval.

Source YAML

icd_o_3_morphology8804/3
icd_o_3_topography["C49"]
icd_10C49
who_classificationWHO Soft Tissue Tumours 5th ed (2020): Epithelioid sarcoma

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Notes

Epithelioid sarcoma is defined by SMARCB1/INI1 loss and has historically poor prognosis in the proximal/aggressive variant. Tazemetostat (EZH2 inhibitor) is FDA-approved (2020) for metastatic or locally advanced epithelioid sarcoma not eligible for complete resection — the first and only FDA-approved targeted therapy. INI1 loss (detected by IHC) is the companion diagnostic. ORR ~15% in EZH-202 but durable responses seen. Note: tazemetostat is also approved for EZH2-mutant follicular lymphoma (different indication/biomarker). Distal-type has better prognosis than proximal-type; lymph node metastases are common (30%).

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