Lomustine
From Anvita Health Wiki
Contents |
Introduction
- Tradename: CeeNu.
Indications
Dosage
- 100-130 mg/m2 once every 6 weeks
- reduce dose 25% for creatinine clearance of 10-50 mL/min
- 50% reduction in dosage if creatinine clearance < 10 mL/min
- Capsule: 10, 40, 100 mg.
Pharmacokinetics
- well absorbed orally
- distributes to all tissues
- concentrated in the CSF
- metabolized by the liver
- eliminated in the urine
- dose reductions recommended in renal dysfunction
- 1/2life is approximately 70 hours
- not dialyzable
Adverse-effects
- common (> 10%)
-
- occurs 3-6 hours after oral administration
- emetic potential high
- 60-90% < 60 mg
- > 90% > 60 mg
- onset 14 days
- nadir 4-5 weeks
- recovery 6 weeks
- less common (1-10%)
- uncommon (< 1%)
- hepatotoxicity, alopecia, renal failure, pulmonary fibrosis with cumulative doses > 600 mg, disorientation, lethargy, ataxia, dysarthria
- Toxicity:
- No known antidotes
- Treatment of toxicity is symptomatic & supportive
- drug adverse effects of alkylating agents
Drug-interactions
- cimetidine may increase myelosuppression
- phenobarbital
Mechanism-of-action
- alkylating agent
- interferes with DNA & RNA synthesis
More General Terms
Internet Database
PubChem: 3950
References
- Kaiser Permanente Northern California Regional Drug Formulary, 1998
- Drug Information & Medication Formulary, Veterans Affairs, Central California Health Care System, 1st ed., Ravnan et al eds, 1998
