
CLOFARABINE
| Clofarabine (clo-fa-ra'been) Clolar Classifications: antineoplastic; purine antimetabolite; Therapeutic: antineoplastic; antimetabolite Prototype: 6-Mercaptopurine Pregnancy Category: D |
Availability
1 mg/mL injection.
Action
Clofarabine inhibits DNA repair within cancer cells, thus interfering with mitosis; it also disrupts the mitochondrial membrane, leading to cancer cell death.
Therapeutic Effect
Cytotoxic to rapidly proliferating and quiescent cancer cells.
Uses
Treatment of persons 121 y of age with relapsed or refractory acute lymphocytic leukemia (ALL) after at least 2 prior regimens.
Contraindications
Severe bone marrow suppression; active infection; pregnancy (category D); lactation.
Cautious Use
Renal or hepatic function impairment; thrombocytopenia; neutropenia; previous chemotherapy or radiation therapy; females of childbearing age; history of viral infections such as herpes; history of cardiac disease or hypotension.
Route & Dosage
| Acute Lymphocytic Leukemia Adult/Adolescent/Child: IV 52 mg/m2/d for 5 d |
Administration
- Do not give drugs with known renal toxicity during the 5 d of clofarabine administration.
| Intravenous PREPARE: IV Infusion: Withdraw required dose from vial using a 0.2 micron filter syringe. Further dilute with D5W or NS prior to infusion. ADMINISTER: IV Infusion: Give over 2 h. Note: It is recommended that IV fluids be given continuously throughout the 5 d of clofarabine administration. |
- Store diluted solution at room temperature. Use within 24 h of mixing.
Adverse Effects (≥1%)
CNS: Anxiety, depression, dizziness, headache, irritability, somnolence. CV: Tachycardia, pericardial infusion, left ventricular systolic dysfunction (LSVT). GI: Vomiting, nausea, and diarrhea, abdominal pain, constipation. Hematologic/Lymphatic: Anemia, leukopenia, thrombocytopenia, neutropenia, febrile neutropenia. Hepatic: Jaundice, hepatomegaly. Metabolic: Anorexia, decreased appetite, edema, decreased weight. Musculoskeletal: Arthralgia, back pain, myalgia. Respiratory: Cough, dyspnea, epistaxis, pleural effusion, respiratory distress. Skin: Dermatitis, contusion, dry skin, erythema, palmar-plantar erythrodysesthesia syndrome, pruritus. Body as a Whole: Increase risk of infection.Pharmacokinetics
Distribution: 47% protein bound. Metabolism: Negligible. Elimination: Primarily unchanged in the urine. Half-Life: 5.2 h.Nursing Implications
Assessment & Drug Effects
- Monitor vital signs frequently during infusion of clofarabine.
- Monitor closely for S&S of capillary leak syndrome or systemic inflammatory response syndrome (e.g., tachypnea, tachycardia, hypotension, pulmonary edema). If either is suspected, immediately DC IV, institute supportive measures and notify physician.
- Monitor I&O rates and pattern and watch for S&S of dehydration, including dizziness, lightheadedness, fainting spells, or decreased urine output.
- Withhold drug and notify physician if hypotension develops for any reason during 5-d period of drug administration.
- Lab tests: Baseline and periodic CBC and platelet counts (more frequent with cytopenias); frequent LFTs and kidney function test during the 5 d of clofarabine therapy.
Patient & Family Education
- Report any distressing adverse effect of therapy to physician.
- Use effective measures to avoid pregnancy while taking this drug.
Canadian drug name;
Prototype drug