Drug Guide
Streptozocin
Classification
Therapeutic: Antineoplastic, Alkylating agent
Pharmacological: Nitrosourea compound, Alkylating agent
FDA Approved Indications
- Treatment of pancreatic islet cell carcinoma
Mechanism of Action
Streptozocin is a nitrosourea compound that acts as an alkylating agent, causing DNA damage in cancer cells, leading to cell death, particularly in pancreatic islet cell tumors.
Dosage and Administration
Adult: Typically 500 mg/m² IV once a day for 5 consecutive days, repeated every 4-6 weeks, adjusted based on response and tolerability.
Pediatric: Safety and efficacy not established; use with caution and under specialist supervision.
Geriatric: Adjust dosage based on renal function and tolerability.
Renal Impairment: Use cautiously; may require dose adjustment due to increased toxicity risk.
Hepatic Impairment: Use cautiously; no specific dosage recommendation available.
Pharmacokinetics
Absorption: Administered IV, so absorption is complete and rapid.
Distribution: Widely distributed; crosses the blood-brain barrier.
Metabolism: Metabolized minimally; undergoes hepatic processing.
Excretion: Primarily excreted via the kidneys.
Half Life: Approximately 15-20 minutes in plasma.
Contraindications
- Hypersensitivity to streptozocin or other nitrosoureas.
- Pre-existing renal or hepatic impairment.
Precautions
- Monitor renal and hepatic function closely.
- Risk of myelosuppression, nephrotoxicity, and neurotoxicity.
- Use with caution in pregnant or breastfeeding women; potential teratogenicity and risk to infant.
Adverse Reactions - Common
- Nausea and vomiting (Common)
- Myelosuppression (anemia, leukopenia, thrombocytopenia) (Common)
- Nephrotoxicity (Common)
Adverse Reactions - Serious
- Neurotoxicity (including seizures, coma) (Serious)
- Secondary malignancies (rare) (Rare)
Drug-Drug Interactions
- Other myelosuppressive agents, nephrotoxic drugs, or hepatotoxic drugs.
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Monitor blood counts, renal and hepatic function regularly.
Diagnoses:
- Risk for infection due to myelosuppression.
- Risk for renal impairment.
Implementation: Administer IV as ordered, monitor vital signs and lab values, manage side effects, ensure hydration.
Evaluation: Assess response to therapy and toxicity; adjust treatment as necessary.
Patient/Family Teaching
- Report signs of infection, bleeding, or unusual neuro symptoms promptly.
- Maintain adequate hydration.
- Avoid pregnancy.
Special Considerations
Black Box Warnings:
- Risk of severe myelosuppression leading to infections.
- Potential for secondary malignancies.
Genetic Factors: N/A
Lab Test Interference: May cause transient increases in serum transaminases and serum creatinine; interpret lab results with caution.
Overdose Management
Signs/Symptoms: Severe myelosuppression, neurotoxicity, nephrotoxicity.
Treatment: Supportive care, intensive monitoring, possible use of growth factors, renal support if needed.
Storage and Handling
Storage: Store at room temperature, protected from light.
Stability: Stable when stored properly, discard any unused portion after designated expiration.