ACG Case Reports Journal · 2019 · 11 citations · 5 references
PharmacyPharmacologyPharmacotherapyClinical PharmacologyHepatologyHepatotoxicologyHepatic Dose ModificationHepatic ImpairmentHepatic ToxicityHepatotoxicity ManagementLiver DiseaseMonitoring In Hepatic ImpairmentChronic Myeloid Leukemia TherapyDose-related Liver ToxicityDrug-induced Liver Injury MonitoringHepatic Function TestsHepatic Safety PharmacologyLiver Toxicity AssessmentTyrosine Kinase Inhibitor HepatotoxicityTyrosine Kinase Inhibitor Therapy
Idiosyncratic hepatotoxicity is a leading reason for the discontinuation or dose modification of Food and Drug Administration (FDA)-approved medications in the United States. We report the case of a 53-year-old woman with chronic myeloid leukemia who developed acute cholestatic hepatitis in response to the tyrosine kinase inhibitor nilotinib. Nilotinib was discontinued, and the patient's liver function tests normalized over the next 3 months. We conclude that nilotinib may cause life-threatening hepatotoxicity and recommend that patients on the medication undergo regular monitoring of their liver tests.
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Nilotinib versus Imatinib for Newly Diagnosed Chronic Myeloid Leukemia
Giuseppe Saglio, Dong‐Wook Kim, Surapol Issaragrisil et al. · New England Journal of Medicine · 2010 · 1.7K citations · Full text
Hagop M. Kantarjian, Francis J. Giles, Norbert Gattermann et al. · Blood · 2007 · 745 citations · Full text
Medicine, Oncology, Pharmacology +9
UGT1A1 promoter polymorphism increases risk of nilotinib-induced hyperbilirubinemia
Jonathan B. Singer, Yaping Shou, Francis J. Giles et al. · Leukemia · 2007 · 122 citations