Drug Guide
Vincristine Sulfate
Classification
Therapeutic: Antineoplastic agent
Pharmacological: Vinca alkaloid
FDA Approved Indications
- Acute lymphoblastic leukemia (ALL)
- Hodgkin's lymphoma
- Non-Hodgkin's lymphomas
- Neuroblastoma
- Wilms tumor
Mechanism of Action
Vincristine binds to tubulin, inhibiting microtubule formation in mitotic spindle fibers, leading to cell cycle arrest at metaphase and apoptosis.
Dosage and Administration
Adult: Dosage varies based on condition; typical dose is 1.4 mg/m^2 IV once weekly. Careful dose adjustments are necessary for toxicity.
Pediatric: Typically 0.05 to 0.16 mg/kg IV weekly, not exceeding adult dose, with adjustments based on response and toxicity.
Geriatric: Use with caution; monitor for increased toxicity.
Renal Impairment: Adjust dosage as needed; no specific guidelines but monitor closely.
Hepatic Impairment: Use caution; no specific guidelines—monitor for toxicity.
Pharmacokinetics
Absorption: Not applicable (administered IV).
Distribution: Wide distribution; crosses blood-brain barrier to some extent.
Metabolism: Hepatic metabolism; primarily through cytochrome P450 enzymes.
Excretion: Primarily via bile; small amount via urine.
Half Life: Approximately 85 hours in adults.
Contraindications
- Hypersensitivity to vincristine or other vinca alkaloids.
Precautions
- Neurotoxicity risk — monitor neurological status, avoid intrathecal administration.
- Leukopenia, gastrointestinal disturbances, and SIADH should be monitored.
- Pregnancy — teratogenic, and potential fetal harm. Use during pregnancy only if clearly needed.
Adverse Reactions - Common
- Peripheral neuropathy (Common)
- Hair loss (Less common)
- Constipation (Common)
- SIADH (syndrome of inappropriate antidiuretic hormone secretion) (Less common)
Adverse Reactions - Serious
- Severe neurotoxicity (e.g., seizures, paralysis) (Rare)
- Myelosuppression (neutropenia, thrombocytopenia) (Less common)
- Extravasation leading to tissue necrosis (Serious, if occurs)
Drug-Drug Interactions
- Potential additive neurotoxicity with other neurotoxic agents
- Caution with CYP3A4 inhibitors/inducers affecting metabolism.
Drug-Food Interactions
N/ADrug-Herb Interactions
N/ANursing Implications
Assessment: Neurological status, complete blood counts, signs of extravasation.
Diagnoses:
- Risk for peripheral neurotoxicity
- Risk for infection due to myelosuppression
Implementation: Administer IV as prescribed, monitor IV site for extravasation, provide supportive care for side effects.
Evaluation: Assess for neurotoxicity, hematologic response, and overall patient tolerance.
Patient/Family Teaching
- Report numbness, tingling, weakness or paralysis.
- Avoid contact with people with infections due to immunosuppression.
- Report signs of tissue necrosis at injection site.
Special Considerations
Black Box Warnings:
- Neurotoxicity — risk of irreversible effects.
Genetic Factors: None specific.
Lab Test Interference: May cause false-positive tests for bilirubin or certain enzymes.
Overdose Management
Signs/Symptoms: Severe neurotoxicity, paralysis, seizures.
Treatment: Supportive care; no specific antidote. Immediate discontinuation and supportive measures are essential.
Storage and Handling
Storage: Store at controlled room temperature, away from light.
Stability: Stable at room temperature for the duration of the shelf life.