Drug Guide
Vinorelbine Tartrate
Classification
Therapeutic: Antineoplastic agent
Pharmacological: Vinca alkaloid
FDA Approved Indications
- Non-small cell lung cancer (NSCLC)
- Breast cancer (adjuvant and metastatic)
Mechanism of Action
Vinorelbine inhibits microtubule polymerization by binding to tubulin, disrupting mitotic spindle formation, thereby arresting cell division in metaphase and inducing apoptosis.
Dosage and Administration
Adult: Typically 25 mg/m^2 IV on days 1 and 8 of a 21-day cycle, but regimens vary based on indication and patient response.
Pediatric: Use is investigational; dosing based on body surface area with close monitoring.
Geriatric: Adjustments based on renal and hepatic function; monitor closely due to increased sensitivity.
Renal Impairment: Use with caution; may require dose adjustment based on degree of impairment.
Hepatic Impairment: Reduce dose in patients with hepatic dysfunction due to decreased metabolism.
Pharmacokinetics
Absorption: Administered intravenously; no oral absorption.
Distribution: Widely distributed, crosses the blood-brain barrier.
Metabolism: Metabolized in the liver via CYP3A4 enzymes.
Excretion: Excreted primarily in feces; small amount in urine.
Half Life: Approximately 40-50 hours.
Contraindications
- Hypersensitivity to vinorelbine or other vinca alkaloids.
- Severe myelosuppression.
- Pregnancy (category D).
Precautions
- Monitor blood counts regularly.
- Assess hepatic and renal function before and during treatment.
- Use caution in patients with infections or other comorbidities.
Adverse Reactions - Common
- Myelosuppression (neutropenia, thrombocytopenia, anemia) (Very common)
- Nausea and vomiting (Common)
- Alopecia (Common)
- Peripheral neuropathy (Uncommon)
Adverse Reactions - Serious
- Severe neutropenia leading to infection (Possible)
- Thrombocytopenia leading to bleeding (Possible)
- Severe hypersensitivity reactions (Rare)
Drug-Drug Interactions
- CYP3A4 inhibitors (azole antifungals, macrolides) increase vinorelbine levels.
- CYP3A4 inducers (rifampin, carbamazepine) decrease efficacy.
Drug-Food Interactions
- Grapefruit juice may increase plasma levels.
Drug-Herb Interactions
N/ANursing Implications
Assessment: Monitor blood counts frequently, especially ANC.
Diagnoses:
- Risk for infection due to myelosuppression.
- Risk for bleeding due to thrombocytopenia.
Implementation: Administer IV as scheduled, monitor for signs of infection, bleeding, and peripheral neuropathy.
Evaluation: Assess blood counts, neurological status, and patient response to therapy.
Patient/Family Teaching
- Report any signs of infection, unusual bleeding, or severe neuropathy.
- Follow instructions for managing side effects.
- Avoid live vaccines during therapy.
Special Considerations
Black Box Warnings:
- Severe neutropenia leading to infection and death. Cannot be used in pregnancy due to teratogenicity.
Genetic Factors: CYP3A4 genetic polymorphisms can affect metabolism.
Lab Test Interference: May cause falsely low serum cholinesterase levels.
Overdose Management
Signs/Symptoms: Severe myelosuppression, neurotoxicity.
Treatment: Supportive care including growth factor support, blood and platelet transfusions, symptomatic management.
Storage and Handling
Storage: Store vials under refrigeration at 2-8°C.
Stability: Stable for specified period per manufacturer instructions.