Cytarabine (Arabinofuranosyl Cytidine, ARA-C, Cytosine Arabinoside, Cytosar-U)
Indications
- Acute Myeloid Leukemia (AML) (see Acute Myeloid Leukemia, [[Acute Myeloid Leukemia]]): prior to bone marrow transplant
- Non-Hodgkin’s Lymphoma (see Lymphoma, [[Lymphoma]])
Pharmacology
- Pyrimidine Analog Which Impairs DNA Synthesis: specific for the S-phase of the cell cycle
- Cytarabine is Rapidly Converted into Cytosine Arabinoside Triphosphate -> Cell Cycle is Held in the S Phase: impairs DNA synthesis
- This most impacts rapidly dividing cells, which require DNA replication for mitosis
- Cytarabine Inhibits DNA/RNA Polymerases and Nucleotide Reductase: these enzymes are required for DNA synthesis
- Inhibits Deoxycytidine Utilization: when used as an anti-viral
Administration
Dose Adjustment
Adverse Effects
Gastrointestinal Adverse Effects
- Acute Pancreatitis (see Acute Pancreatitis, [[Acute Pancreatitis]]): questionable association
Neurologic Adverse Effects
Pulmonary Adverse Effects
Acute Lung Injury-ARDS (see Acute Lung Injury-ARDS, [[Acute Lung Injury-ARDS]])
- Epidemiology: associated with intensive regimens
- Clinical
- Timing of Onset
- 13-28% developed their lung injury during ARA-C administration
- 50% developed lung injury during within a month of completing ARA-C administration
- Treatment: supportive
- Prognosis: may be fatal
Other Adverse Effects
References