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# vincristine
## Overview
- **Classification**: Mitotic inhibitor, Vinca alkaloid, Antineoplastic agent
- **Mechanism**: Binds to tubulin, inhibiting microtubule polymerization, causing mitotic arrest at metaphase and resulting in cell death[1][2][3][6].
## Primary Indications
1. **Acute lymphoblastic leukemia (ALL)** – Used in induction and combination chemotherapy regimens
2. **Non-Hodgkin lymphoma (NHL) and Hodgkin lymphoma** – Part of multi-agent chemo protocols
3. **Other cancers** – Neuroblastoma, Wilms' tumor, Ewing sarcoma, rhabdomyosarcoma, small cell lung cancer, and others[1][3][6].
## Adult Dosing
### Standard Dosing
**Acute lymphoblastic leukemia, lymphoma, and other malignancies**
- **Dose**: 1.4 mg/m² (max 2 mg per dose)
- **Frequency**: Once weekly or as per protocol
- **Route**: Intravenous (IV) infusion, slow push or infusion
- **Duration**: Based on chemotherapy regimen
### Dose Adjustments
- **Renal impairment**: No specific dosing adjustments recommended; use caution
- **Hepatic impairment**: Reduce dose by 50% if bilirubin 1.5–3 mg/dL; consider withholding if bilirubin >3 mg/dL due to reduced metabolism and increased toxicity risk[1][6]
- **Elderly patients**: No formal adjustment, but monitor closely for neurotoxicity
## Pediatric Dosing
### Neonates (0-28 days)
- **Dose**: 0.01–0.05 mg/kg
- **Frequency**: Weekly
- **Maximum**: Usually capped at 0.05 mg/kg or 2 mg max
- **Special Notes**: Careful monitoring due to immature liver function affecting metabolism
### Infants (1-12 months)
- **Dose**: 0.05 mg/kg
- **Frequency**: Weekly
- **Maximum**: 2 mg per dose
### Children (1-12 years)
- **Dose**: 1.5–2 mg/m² (max 2 mg) once weekly
- **Frequency**: Weekly
- **Maximum**: Adult dose equivalent (2 mg max)
### Adolescents (13-18 years)
- **Dose**: Use adult dosing (1.4 mg/m², max 2 mg)
- **Maximum**: 2 mg per dose
## Safety Information
### Contraindications
- **Absolute**: Intrathecal administration (fatal if given intrathecally)
- **Absolute**: Hypersensitivity to vincristine or any component
- **Relative**: Pre-existing peripheral neuropathy or demyelinating conditions (e.g., Charcot-Marie-Tooth syndrome)[5]
### Common Adverse Effects
- **Very Common (>10%)**: Peripheral neuropathy (sensory and motor), constipation/ileus
- **Common (1-10%)**: Jaw pain, SIADH, mild myelosuppression (rare), phlebitis at injection site
- **Serious but Rare**: Severe neurotoxicity (autonomic neuropathy, cranial nerve palsies), seizures, paralytic ileus, tumor lysis syndrome
### Key Drug Interactions
- **CYP3A4 inhibitors (e.g., azole antifungals, macrolides)**: Increased vincristine toxicity; monitor closely for neurotoxicity
- **P-glycoprotein inhibitors**: May increase vincristine levels; dose adjustment may be needed
- **Other neurotoxic drugs (e.g., other vinca alkaloids, cisplatin)**: Increased risk of additive neuropathy
## Monitoring & Follow-up
- **Before Treatment**: Baseline neurologic exam, liver function tests (LFTs), complete blood count (CBC)
- **During Treatment**: Monitor neurologic status weekly, LFTs periodically, and bowel function
- **Clinical Signs**: Watch for peripheral neuropathy signs, constipation/ileus, jaw pain, weakness
## Clinical Pearls
- 💡 **Avoid intrathecal administration at all costs** — fatal neurotoxicity occurs
- 💡 **Monitor liver function closely** to avoid toxicity, as vincristine is hepatically metabolized
- 💡 **Counsel patients on constipation prevention** and neurologic symptoms to report early
> **⚠️ Important**: This information is for educational purposes only. Always consult current prescribing information, local guidelines, and clinical judgment before prescribing.