OpenOnco
UA EN

Onco Wiki / Drug

Brentuximab vedotin

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

IDDRUG-BRENTUXIMAB-VEDOTIN
TypeDrug
Aliases
AdcetrisБрентуксимаб ведотин
Statusreviewed 2026-04-25 | pending_clinical_signoff
DiseasesDIS-AITL DIS-ALCL DIS-CHL DIS-MF-SEZARY
SourcesSRC-NCCN-BCELL-2025

Drug Facts

ClassAnti-CD30 antibody-drug conjugate (MMAE payload)
MechanismCD30-targeted IgG1 conjugated to MMAE via cleavable linker — internalized by CD30+ cells, releases MMAE intracellularly → microtubule disruption → apoptosis.
Typical dosingALCL/PTCL CD30+ 1L (CHP-Bv): 1.8 mg/kg IV day 1 of 21-day cycle × 6. Hodgkin 1L (A+AVD): 1.2 mg/kg IV days 1+15 of 28-day cycle × 6. Mycosis fungoides r/r (CD30+ ≥10%): 1.8 mg/kg IV every 3 weeks.
Ukraine registeredTrue
NSZU reimbursedTrue
Ukraine last verified2026-04-27

Warnings

Notes

Used in: 1L T-cell lymphomas with CD30+ (ALCL universal CD30+; ~40-60% PTCL NOS / AITL CD30+) — ECHELON-2 trial showed CHP-Bv superior to CHOP. 1L Hodgkin (A+AVD = ABVD with brentuximab replacing bleomycin — ECHELON-1; bleomycin removed due to lung toxicity additive risk). R/R cutaneous lymphomas (MF/Sézary CD30+, primary cutaneous ALCL). NEVER combine with bleomycin. Ukraine: registered, NOT НСЗУ-reimbursed.

Used By

Contraindications

Regimens