Classes
DEA Class; Rx
Common Brand Names; Tasigna
- Antineoplastics, Tyrosine Kinase Inhibitor
Description
BCR-ABL tyrosine kinase inhibitor
Used in certain types of Philadelphia chromosome-positive chronic myelogenous leukemia
May cause QT prolongation; sudden death has been reported
Indications
Indicated for the treatment of Philadelphia chromosome-positive (Ph+) chronic myelogenous leukemia (CML).
Contraindications
Long QT syndrome, hypokalemia, hypomagnesemia
Adverse Effects
- Rash (33%)
- Headache (31%)
- Nausea (31%)
- Pruritus (29%)
- Fatigue (28%)
- Pyrexia (24%)
- Diarrhea (22%)
- Constipation (21%)
- Vomiting (21%)
- Arthralgia (18%)
- Cough (17%)
- Extremity pain (16%)
- Asthenia (14%)
- Muscle spasms (14%)
- Myalgia (14%)
- Abdominal pain (13%)
- Bone pain (13%)
- Back pain (12%)
- Dyspnea (11%)
- Nasopharyngitis (11%)
- Peripheral edema (11%)
Warnings
Grade 3/4 thrombocytopenia, neutropenia and anemia may occur; perform complete blood cell counts (CBC) every 2 weeks for first 2 months and then monthly thereafter, or as clinically indicated; myelosuppression was generally reversible and usually managed by withholding drug temporarily or dose reduction
Sudden deaths reported; ventricular repolarization abnormalities may have contributed to their occurrence; evaluate cardiovascular status and monitor/manage cardiovascular risk factors during therapy
QT interval reported; significant prolongation of the QT interval may occur when drug is inappropriately taken with food; avoid taking with food; prolongation of the QT interval can result in torsade de pointes, which may result in syncope, seizure, and/or death
May cause hypophosphatemia, hypokalemia, hyperkalemia, hypocalcemia, and hyponatremia; correct hypokalemia or hypomagnesemia before administration; monitor periodically during therapy
Cardiovascular events (eg, ischemic heart disease, peripheral arterial occlusive disease, ischemic cerebrovascular events) reported in patients with newly diagnosed Ph+ CML; evaluate cardiovascular status, monitor cardiovascular risk factors, and manage during therapy
Use caution in history of pancreatitis; monitor serum lipase monthly or as clinically indicated; in case lipase elevations are accompanied by abdominal symptoms, interrupt doses and consider appropriate diagnostics to exclude pancreatitis
Use caution in hepatic impairment; monitor hepatic function tests (HFTs) monthly or as clinically indicated; reduce dose and monitor QT interval
Pregnancy and Lactation
No available data in pregnant women to inform the drug-associated risk
No data are available regarding the presence of nilotinib or its metabolites in human milk or its effects on a breastfed child or on milk production
Maximum Dosage
800 mg/day PO.
800 mg/day PO.
230 mg/m2 twice daily, not to exceed 400 mg/dose.
230 mg/m2 twice daily, not to exceed 400 mg/dose.
Safety and efficacy have not been established.
How supplied
Nilotinib
capsule
- 150mg
- 200mg