Durvalumab consolidation post-CRT (NSCLC stage III unresectable)
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.
| Components | DRUG-DURVALUMAB |
|---|
| ID | REG-DURVA-CONSOLIDATION-PACIFIC |
|---|---|
| Type | Regimen |
| Status | pending_clinical_signoff |
| Diseases | None declared |
| Sources | SRC-ESMO-NSCLC-EARLY-2024 SRC-NCCN-NSCLC-2025 |
Notes
PACIFIC: 5-year OS 43% (durva) vs 33% (placebo) post-concurrent CRT in stage III unresectable NSCLC. Standard of care.
Used By
Indication
IND-NSCLC-STAGE-III-PACIFIC- IND-NSCLC-STAGE-III-PACIFIC