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Epoetin alfa / Darbepoetin alfa

Deterministic view of the source YAML entity. Clinical authority remains with the cited source IDs and reviewer sign-off state.

IDDRUG-EPOETIN-ALFA
TypeDrug
Aliases
Aranesp (darbepoetin)ESAEpogenEprexErythropoiesis-stimulating agentProcritrHuEPOЕпоетин альфа / Дарбепоетин альфа
Statusreviewed 2026-04-25 | pending_clinical_signoff
DiseasesDIS-MDS-LR
SourcesSRC-ESMO-MDS-2021 SRC-NCCN-AML-2025

Drug Facts

ClassErythropoiesis-stimulating agent (ESA, recombinant erythropoietin)
MechanismRecombinant human erythropoietin / hyperglycosylated analog (darbepoetin). Binds erythroid progenitor EPO receptor → erythroid expansion. 1L for symptomatic anemia in lower-risk MDS with low endogenous EPO (≤500 mU/mL) and modest transfusion burden (≤2U/mo).
Typical dosingMDS-LR anemia: epoetin alfa 60,000 IU SC weekly OR darbepoetin 150-300 μg SC weekly. Re-evaluate at 8-12 weeks; if Hb response (≥1.5 g/dL rise) → continue, else discontinue. Target Hb 11-12 g/dL (do not exceed).
Ukraine registeredTrue
NSZU reimbursedTrue
Ukraine last verified2026-04-27

Warnings

Notes

MDS-LR 1L for symptomatic anemia if endogenous EPO ≤500 mU/mL AND TD ≤2U/month — response rate ~50-60% in this selected population. Add G-CSF in non-responders if RS-MDS. Target Hb 10-12 g/dL — do NOT exceed (boxed warning). Iron supplementation as needed. Switch to luspatercept on ESA failure (MEDALIST) — both reimbursement-asymmetric in Ukraine (ESA reimbursed, luspatercept not).

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Regimens