Soft tissue sarcoma (STS) · None
Deterministic view of the source YAML entity. Clinical authority remains with the cited source IDs and reviewer sign-off state.
Knowledge-base record for audit. Provisional clinical content: this is not a prescription. An oncologist must verify original sources, applicability and review status. Full rules and constraints are in the YAML.
| Track | standard |
|---|---|
| Linked regimen | None |
| ID | IND-COSTELLO-CARRIER-SURVEILLANCE |
|---|---|
| Type | Indication |
| Status | reviewed 2026-05-19 | pending_clinical_signoff |
| Diseases | DIS-SOFT-TISSUE-SARCOMA |
| Sources | SRC-ESMO-SARCOMA-2024 SRC-NCCN-BLADDER-2025 SRC-NCCN-GENETIC-FAMILIAL-BREAST-OVARIAN-2025 |
Notes
STUB pending two-Co-Lead signoff per CHARTER §6.1 dev-mode. Standard-track Costello-syndrome confirmed-carrier surveillance per Gripp / Costello Syndrome Family Network consensus. Disease anchor DIS-SOFT-TISSUE-SARCOMA covers embryonal RMS; neuroblastoma + bladder TCC cancer-spectrum noted in rationale.
Used By
Indication
IND-COSTELLO-CARRIER-INTENSIFIED- IND-COSTELLO-CARRIER-INTENSIFIED