Infusion reaction rescue protocol (mAb / chemotherapy IRR Grade ≥2)
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-DEXAMETHASONE |
|---|
| ID | REG-IRR-RESCUE-PROTOCOL |
|---|---|
| Type | Regimen |
| Status | reviewed 2026-04-27 | pending_clinical_signoff |
| Diseases | None declared |
| Sources | SRC-ESMO-DLBCL-2024 SRC-NCCN-BCELL-2025 |
Notes
CTCAE v5.0 IRR grading + NCCN/ESMO/MASCC anaphylaxis management framework. Highest-risk agents for IRR: rituximab cycle 1 (~75% any-grade, ~10% G3+), obinutuzumab cycle 1 day 1 (~65%), daratumumab cycle 1 (~50% IV; ~13% SC), amivantamab cycle 1 day 1 (~65% IV; ~13% SC), cetuximab cycle 1 (~3% G3+; SE US ~20% with alpha-gal IgE), paclitaxel (~10% any-grade; cremophor vehicle hypersensitivity), carboplatin/oxaliplatin (cumulative; cycles 6+ — true IgE-mediated, desensitization protocol indicated), L-asparaginase (anaphylaxis ~5-10% with native E. coli formulation; less with PEG-asparaginase / Erwinia), bleomycin (rare; idiosyncratic). Premedication standard: acetaminophen 650-1000 mg PO + diphenhydramine 25-50 mg PO/IV + ranitidine 50 mg IV (or famotidine 20 mg IV) ≥30 min before infusion; add IV steroid for high-risk agents (rituximab cycle 1, obinutuzumab cycle 1, daratumumab cycle 1, amivantamab cycle 1, taxanes). Slow first-cycle infusion rate is universally protective. Desensitization (incremental dose escalation over 3-4h with 12-step protocol) allows continuation of life-saving therapy in true IgE-mediated reactions — requires allergy/immunology + ICU-capable setting.
Used By
No reverse references found in the YAML corpus.