Drug Guide
Altretamine
Classification
Therapeutic: Antineoplastic agent
Pharmacological: Alkylating agent
FDA Approved Indications
- Ovarian cancer, persistent or recurrent
Mechanism of Action
Altretamine is an alkylating agent that interferes with DNA synthesis by forming cross-links, leading to cell death, particularly in ovarian cancer cells.
Dosage and Administration
Adult: Initially, 5 mg orally 4 times daily for 14 days, then 2-week rest, repeating cycles.
Pediatric: Not typically used in pediatric patients.
Geriatric: No specific dose adjustment; monitor for toxicity.
Renal Impairment: Use with caution; no specific adjustments provided.
Hepatic Impairment: Use with caution; no specific adjustments provided.
Pharmacokinetics
Absorption: Well absorbed orally.
Distribution: Widely distributed, crosses the blood-brain barrier.
Metabolism: Hepatic, primarily via demethylation.
Excretion: Renal, mainly as metabolites.
Half Life: Approximately 8 hours.
Contraindications
- Known hypersensitivity
Precautions
- Monitor blood counts regularly, as myelosuppression is common.
- Use with caution in hepatic impairment.
- Potential for neurotoxicity and other adverse effects; adjust dose or discontinue as needed.
Adverse Reactions - Common
- Nausea, vomiting (Common)
- Myelosuppression (Common)
- Alopecia (Less common)
Adverse Reactions - Serious
- Bone marrow suppression leading to anemia, leukopenia, thrombocytopenia (Serious)
- Neurotoxicity (peripheral neuropathy) (Less common)
- Hemorrhagic cystitis (Less common)
Drug-Drug Interactions
- CNS depressants, other myelosuppressive agents
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor CBC regularly, assess for signs of neurotoxicity and other adverse effects.
Diagnoses:
- Risk for infection related to myelosuppression.
- Risk for tissue injury related to hemorrhagic cystitis.
Implementation: Administer as prescribed, monitor blood counts, provide supportive care.
Evaluation: Assess for response to therapy and adverse effects, adjust treatment plan accordingly.
Patient/Family Teaching
- Report signs of infection, bleeding, or unusual neurological symptoms.
- Use effective contraception during therapy and for at least 6 months after.
- Avoid alcohol and hepatotoxic drugs.
- Attend regular blood tests as scheduled.
Special Considerations
Black Box Warnings:
- Potentially severe myelosuppression, including leukopenia and thrombocytopenia, which can be life-threatening.
Genetic Factors: None specified.
Lab Test Interference: May affect hepatic and hematologic laboratory tests.
Overdose Management
Signs/Symptoms: Severe myelosuppression, neurological symptoms.
Treatment: Supportive care including growth factors, transfusions, and symptomatic management; no specific antidote.
Storage and Handling
Storage: Store at room temperature, protected from light and moisture.
Stability: Stable when stored properly, check expiration date regularly.