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μνλΌλΉ(νν **Ara-C**λ‘ λΆλ¦Ό)μ μ£Όλ‘ κ°μ κ³ μμ΄μ λ¦Όνλ§λ΄κ³ μ’ μ, 골μμ¦μμ± μ§ν(λ°±νλ³) λ° μ€μΆμ κ²½κ³ λ¦Όνμ’ μΉλ£μ μ¬μ©λλ ν©μ± νΌλ¦¬λ―Έλ λ΄ν΄λ μ€μλ λμ¬κΈΈνμ μ λλ€. > **μμ μμ :** μ ν΅μ μΈ μ’ μν μΈμλ μνλΌλΉμ μμ μ κ²½νμμ κ°μ **μμΈ λΆλͺ μ μλ§λμΌ(MUE)** λ° μ‘μμ’ μ± μλ§λμΌ(GME)μ λν ν΅μ¬ λ©΄μμ΅μ μλ²μΌλ‘ λ리 μ¬μ©λ©λλ€. μ§μμ μ λ§₯ μ£Όμ (CRI) λλ κ³ μ©λ νΌν μ£Όμ¬ νλ‘ν μ½λ‘ ν¬μ¬ν λ νμ‘λμ₯λ²½μ ν΅κ³Όν μ μμ΄ μ€μΆμ κ²½κ³ μΌμ¦μ± μ§νμ λ§€μ° ν¨κ³Όμ μ λλ€.
μμ© κΈ°μ : Cytarabine is a cell-cycle phase-specific antimetabolite that acts principally during the **S-phase** (active DNA synthesis). * **Intracellular Conversion:** Cytarabine enters the cell and is phosphorylated into its active form, **cytarabine triphosphate**. * **Enzyme Inhibition:** This active metabolite competes with deoxycytidine triphosphate β incorporates into DNA β potently inhibits **DNA polymerase**. * **Result:** Inhibition of DNA synthesis and repair, leading to cell death in rapidly dividing cells. Under certain conditions, it may also block cells from transitioning from the G1 phase to the S phase.
λλ¬Ό μ’ λ³ μ©λ
- Susceptible neoplastic diseases Β· 100 mg/m2 Β· IV/SC Β· continuous infusion over 2-3 days or divided and given IV or SC for 2-4 days Β· 2-4 days Β· Dosed in mg/m2 (NOT mg/kg). Cats are generally dosed similarly to dogs.
- Neoplastic diseases Β· 200-300 mg/m2 (usually 1-1.5 grams per horse per dose) Β· SC/IM/IV Β· every 1-2 weeks Β· Consultation with a veterinary oncologist is encouraged before use.
- Susceptible neoplastic diseases Β· 100 mg/m2 Β· IV/SC Β· continuous infusion over 2-3 days or divided and given IV or SC for 2-4 days Β· 2-4 days Β· Dosed in mg/m2 (NOT mg/kg). Use only as a general guide.
μ©λμ λ©΄ν μμ μ λ¬Έκ°λ₯Ό μν μμ μ°Έκ³ μλ£μ λλ€. νμ μ΅μ λΌλ²¨κ³Ό κ°λ³ νμμ λν΄ νμΈνμμμ€.
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κΈκΈ°
- Hypersensitivity to cytarabine
- Pregnancy (potentially teratogenic and embryotoxic)
μ΄μλ°μ
- Myelosuppression (leukopenia, anemia, thrombocytopenia)
- Anorexia
- Nausea
- Vomiting
- Diarrhea
- Conjunctivitis
- Oral ulceration
- Neurotoxicity
- Hepatotoxicity
- Fever
- Anaphylaxis (rare)
μ½λ¬Ό μνΈμμ©
- Digoxin Β· Cytarabine may decrease the amount of digoxin (tablets only) absorbed after oral dosing due to intestinal mucosa alterations; effect may persist for several days after cytarabine discontinuation.
- Flucytosine (5-FC) Β· Cytarabine may antagonize the anti-infective activity of flucytosine; monitor for decreased efficacy.
- Gentamicin Β· Cytarabine may antagonize the anti-infective activity of gentamicin; monitor for decreased efficacy.
λͺ¨λν°λ§
- Efficacy (tumor response or resolution of neurologic signs)
- Hemograms (mandatory; monitor for myelosuppression, nadir typically at 5-7 days)
- Liver function tests (periodic)
- Kidney function tests (periodic)
κ³Όμ©λ
Efficacy and toxicity are dependent on both the dose and the rate of administration. In dogs, the IV LD50 is 384 mg/kg when given over 12 hours, but drops to 48 mg/kg when infused IV over 120 hours. In the event of an inadvertent overdose, aggressive supportive therapy should be instituted.
VetSheet μ½λ¬Ό λ νΌλ°μ€λ λ©΄ν μμ μ λ¬Έκ°λ₯Ό μν μμ μμ¬κ²°μ 보쑰 λꡬμ΄λ©°, μ λ¬Έμ νλ¨μ΄λ μ μ‘°μ¬μ μ΅μ λΌλ²¨μ λμ νμ§ μμ΅λλ€.