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Procarbazine

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

IDDRUG-PROCARBAZINE
TypeDrug
Aliases
IndicarbMatulaneNatulanПрокарбазин
Statusreviewed 2026-04-26 | pending_clinical_signoff
DiseasesDIS-GLIOMA-LOW-GRADE DIS-PCNSL
SourcesSRC-NCCN-BCELL-2025

Drug Facts

Classalkylating_agent — hydrazine derivative (oral non-classic alkylator)
MechanismMethylhydrazine prodrug undergoing hepatic CYP-mediated oxidation (CYP1A and CYP2B) to azoprocarbazine and ultimately to a methyldiazonium cation that methylates DNA at O6 and N7 of guanine, generating mono- adducts and inhibiting DNA, RNA, and protein synthesis. Lipophilic and crosses the blood-brain barrier — basis of its central role in PCNSL (R-MPV) and Hodgkin (BEACOPP) regimens. Reversibly inhibits monoamine oxidase (weak MAOI activity → tyramine and sympathomimetic interaction syndrome).
Typical dosingPCNSL R-MPV (DeAngelis): 100 mg/m² PO daily × 7 days every 14 days, cycles 1-5 with rituximab + HD-MTX + vincristine; continued in consolidation arms. Hodgkin BEACOPP escalated: 100 mg/m² PO days 1-7 every 21 days × 6 cycles (with bleomycin + etoposide + adriamycin + cyclophosphamide + vincristine + prednisone). PCV (oligodendroglioma): 60 mg/m² PO days 8-21 every 6 weeks.
Ukraine registeredFalse
NSZU reimbursedFalse
Ukraine last verified2026-04-27

Warnings

Notes

Patient counseling on MAOI diet (avoid aged cheese, cured/smoked meats, fermented soy, broad beans, tap beer, draft wine, marmite) is mandatory and must be documented at every cycle. Avoid all SSRIs (fluoxetine, sertraline) and decongestants for 2 weeks after last dose. R-MPV (PCNSL) and BEACOPP-escalated (Hodgkin advanced-stage IPI≥3) are the principal modern uses; both are restricted to specialist centers in UA. AML risk is the dominant late toxicity in Hodgkin survivors and a key reason ABVD remains preferred over BEACOPP in early-stage / lower-IPI disease.

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