- Acute Myeloid Leukemia (AML) – induction and consolidation therapy
Dose:
Induction: 100 mg/m² IV daily for 7 days (standard dose)
Consolidation: 1–3 g/m² IV every 12 hours for 3–5 days, usually after remission
- Acute Lymphocytic Leukemia (ALL) – in combination with other agents
Dose:Combination regimens: Cytarabine is often given 100–200 mg/m² IV daily for 7 days, combined with other agents like methotrexate or vincristine
- Chronic Myelogenous Leukemia (CML) – blast crisis
Dose:Blast crisis: 400–1000 mg/m² IV daily for 7 days (combined with other chemotherapies)
- Non-Hodgkin Lymphoma (NHL) – in combination therapy
- Meningeal Leukemia – intrathecal administration
Dose:Intrathecal injection: 50–75 mg every 2 weeks for consolidation or until remission achieved
- IV infusion vials: 100 mg/mL, 200 mg/mL
- Oral tablets: (rare, but occasionally used in off-label settings)
- Intrathecal (for cerebrospinal fluid administration)
- Injectable formulations: Lyophilized powder for reconstitution (usually for infusion)
- IV infusion: Administer over 1–2 hours, depending on dose
- Intrathecal: Administer via lumbar puncture for direct CSF injection
- Hydration: Use pre- and post-treatment hydration to prevent renal toxicity
- Antiemetics: Often co-administered due to high emetogenic potential
- Monitor blood counts regularly due to myelosuppressive effects
- Class: Antimetabolite (pyrimidine analogue)
- Mechanism of Action:
- Converted to ara-CTP (active form) → inhibits DNA polymerase → interferes with DNA replication → induces apoptosis in rapidly dividing cells
- S-phase specific (acts on cells in DNA synthesis phase)
- Primarily affects hematologic malignancies and dividing cells
- Half-life: ~1–3 hours (depends on dose and route)
- Excretion: Renal (primarily as metabolites)
- Myelosuppression (neutropenia, thrombocytopenia, anemia)
- Nausea/vomiting (high emetogenic potential)
- Mucositis (oral ulcers, GI tract issues)
- Fatigue
- Alopecia (hair loss, generally reversible)
- Rash
- Liver enzyme elevation (mild)
- Hypersensitivity to cytarabine or any of its components
- Severe bone marrow suppression (unless part of treatment)
- Active infections (requires treatment before chemotherapy)
- Pregnancy (category D)
- Myelosuppressive agents: Additive bone marrow suppression (e.g., other chemotherapy agents, certain immunosuppressants)
- Hepatotoxic drugs: Combined hepatotoxicity risk
- Live vaccines: Due to immunosuppression, live vaccines should be avoided during and for several months after cytarabine treatment
- Folic acid: May interfere with cytarabine’s effects (avoid excessive supplementation)
Drug Status
Availability | |
Pregnancy | |
Breastfeeding | |
Schedule |
BRAND NAME | STRENGTH | FORMULATION | PACK SIZE | MANUFACTURER | DISTRIBUTOR |
---|---|---|---|---|---|
Biobin | 100mg/mL | Injection | 1’s | Biochem Pharma | Sai Pharma |
Cytosar | 1000mg/5mL | Injection | 1’s | Pfizer Labs | Pfizer Labs |