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Procarbazine

MATULANE

Pronunciation: proe-KAR-ba-zeen

Procarbazine ballicule: receptor binding, kinetics and half-life diagram
Mechanism of action: Procarbazine ballicule

What it isAlkylating agent generating methyl radicals; Hodgkin lymphoma and brain tumors.

Why this oneIt penetrates the CNS well, which is why it persists in brain tumor regimens.

What limits it⚑ It is a weak MAO inhibitor — tyramine and serotonergic interactions apply. Disulfiram-like reaction with alcohol; secondary leukemia.

Procarbazine molecular structure (skeletal formula)
Molecular structure: Procarbazine

FDA label

BOXED WARNING Administer only by or under supervision of a physician experienced with potent antineoplastic drugs; adequate clinical and laboratory facilities must be available.
FDA dosingPopulationStartTargetMax
Hodgkin lymphoma (single agent)Adult2-4 mg/kg/day x1 week4-6 mg/kg/day until responsemaintenance 1-2 mg/kg/day
Hodgkin lymphoma (single agent)Pediatric50 mg/m²/day x1 week100 mg/m²/day until responsemaintenance 50 mg/m²/day

Renal Undefined

Hepatic Undefined

Instructions

Available strengths

Contraindications

Cautions

Adverse reactions

Pregnancy Can cause fetal harm; teratogenic; advise women of childbearing potential to avoid pregnancy

Lactation Undefined

Cost

Procarbazine (MATULANE)
Strength#/mogeneric $/unitCostPlus
50 mgcapper unitnot offered
NADAC is a voluntary CMS survey of what retail community pharmacies pay for the drugs they stock. Procarbazine is dispensed outside retail pharmacies, so it rarely appears on surveyed invoices.

Generic entryNo US generic

⚠ BOXED WARNING

Classes and tags

Clinical profile

Therapeutic safety burden3 / 4
Overdose danger2 / 4
Weight-gain liability0 / 4
Sedation liability0 / 4
QT / Torsades0 / 4
Direct muscarinic antagonism0 / 4
Embryofetal risk3 / 4

Legacy pregnancy categoryD

Defining liabilityMyelosuppression and agent-specific hepatic, cardiac, pulmonary, neurologic or reproductive toxicity require oncology monitoring.

Serotonin and MAOI

Provisional washout figures

SRI significance0 / 4
MAO-A inhibition2 / 4
Serotonin release0 / 4

Elevating mechanismMAO-A inhibitor

Non-elevating actionNone recorded

Exposure dependenceTherapeutic exposure

Washout AFTER an MAOI14 days

Evidence confidenceHigh

InterpretationAntineoplastic with clinically relevant MAOI activity; manage as an MAOI for PD interaction screening.

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