75 years old or who have comorbidities that prevent the use of intensive induction chemotherapy (in combination with low-dose cytarabine).Contraindicated in:
30 days following treatmentUse Cautiously in:
CV: atrial fibrillation, bradycardia, chest pain, peripheral edema, tachycardia, QT interval prolongation, VENTRICULAR ARRHYTHMIAS.
Derm: rash, alopecia.
F and E: hyperkalemia, hypokalemia, hypomagnesemia, hyponatremia.
GI: abdominal pain, constipation, diarrhea, hyperbilirubinemia, ↑liver enzymes, metallic taste, mucositis, nausea, vomiting.
GU: renal impairment, ↓ fertility (males).
Hemat: anemia, bleeding, neutropenia, thrombocytopenia.
MS: ↑creatine kinase (CK), muscle spasm, pain.
Drug-Drug:
6 cycles (in absence of unacceptable toxicity). Concurrent use of CYP3A inducer: If current dosage 100 mg once daily, ↑ to 200 mg once daily; if current dosage 50 mg once daily, ↑ to 100 mg once daily.Therapeutic Classification: antineoplastics
Pharmacologic Classification: hedgehog pathway inhibitors
Absorption: 77% absorbed following oral administration; absorption ↓ by high-fat, high-calorie foods.
Distribution: Extensively distributed to tissues.
Protein Binding: 91%.
Metabolism/Excretion: Mostly metabolized in the liver by the CYP3A4 isoenzyme, and to some extent by CYP2C8 and UGT1A9. 42% excreted in urine (20% as unchanged drug), 42% excreted in feces (20% as unchanged drug).
Half-life: 17.4 hr.