Vincristine — Drug Monograph
Brand names: Oncovin, Vincasar PFS, Marqibo (liposomal)
Drug class: Vinca Alkaloid
Mechanism of Action
Binds to tubulin and inhibits polymerization of microtubules, causing mitotic arrest at the metaphase plate (M-phase specific). At higher concentrations, depolymerizes existing microtubules. Also inhibits nucleic acid and protein synthesis. Paradoxically, causes peripheral neurotoxicity by disrupting axonal transport.
FDA Indications
- Acute leukemia (ALL) — primary therapy, as part of combination regimens
- Hodgkin lymphoma (MOPP, ABVD-equivalent regimens)
- Non-Hodgkin lymphoma
- Rhabdomyosarcoma
- Neuroblastoma
- Wilms tumor
- Liposomal vincristine (Marqibo): Philadelphia chromosome-negative ALL (second or greater relapse)
Common Side Effects
- Peripheral neuropathy: dose-limiting; sensory-motor-autonomic (glove-and-stocking paresthesias, weakness, foot drop)
- Autonomic neuropathy: constipation, paralytic ileus, urinary retention, orthostatic hypotension
- Alopecia (mild to moderate)
- SIADH
- Jaw pain (after first dose — vincristine-induced pain crisis)
Clinical Pearl
Constipation from vincristine begins with the first dose — prophylactic laxatives (senna, polyethylene glycol) should be prescribed routinely. Autonomic ileus can mimic an acute abdomen. The 2 mg cap on vincristine dosing is debated — some data suggest tall patients (BSA >2 m²) are underdosed and this may reduce efficacy in ALL.
Related Therapies & Mechanisms
- Acalabrutinib (Calquence) — Lymphoma
- Bendamustine (Treanda) — Lymphoma
- Brexucabtagene autoleucel (Tecartus) — Lymphoma
- Cyclophosphamide (Cytoxan) — Lymphoma