Rare Case Presentation of Imatinib Induced Hepatotoxicity

Abstract Imatinib, a tyrosine kinase inhibitor, is a life-saving treatment for Chronic myeloid leukemia (CML) and several other malignancies. Imatinib induced hyperbilirubinemia and hepatic toxicity is seldom reported among all side effects. not a widely known fact. We present a case of a 25 year old male patient who developed hyperbilirubinemia while on imatinib for treatment of CML. On further genetic testing for polymorphism, the patient is homozygous for UGT1A1*28 polymorphism. Due to persistent hyperbilirubinemia while on 400 mg, dose was reduced to 300 mg daily. The patient's hyperbilirubinemia was manageable with a minimal decrement of 25% from the initial dose of imatinib. If handled in a timely fashion by a physician, it helps to control hyperbilirubinemia while the patient receives a reduced dosage of imatinib for life long treatment of CML.

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Publication Details

Journal
Zenodo (CERN European Organization for Nuclear Research)
Published
2025-07-30
DOI
https://doi.org/10.5281/zenodo.18195925
Primary Topic
Chronic Myeloid Leukemia Treatments
Type
article
Field-Weighted Citation Impact
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article

Rare Case Presentation of Imatinib Induced Hepatotoxicity

International Journal of Medical Science and Advanced Clinical Research (IJMACR)
Zenodo (CERN European Organization for Nuclear Research)
Chronic Myeloid Leukemia Treatments
article

Rare Case Presentation of Imatinib Induced Hepatotoxicity

International Journal of Medical Science and Advanced Clinical Research (IJMACR)
article en

Abstract

Abstract Imatinib, a tyrosine kinase inhibitor, is a life-saving treatment for Chronic myeloid leukemia (CML) and several other malignancies. Imatinib induced hyperbilirubinemia and hepatic toxicity is seldom reported among all side effects. not a widely known fact. We present a case of a 25 year old male patient who developed hyperbilirubinemia while on imatinib for treatment of CML. On further genetic testing for polymorphism, the patient is homozygous for UGT1A1*28 polymorphism. Due to persistent hyperbilirubinemia while on 400 mg, dose was reduced to 300 mg daily. The patient's hyperbilirubinemia was manageable with a minimal decrement of 25% from the initial dose of imatinib. If handled in a timely fashion by a physician, it helps to control hyperbilirubinemia while the patient receives a reduced dosage of imatinib for life long treatment of CML.

Zenodo (CERN European Organization for Nuclear Research)
Advanced Pharma (US)
Openalex Percentile: Top 23%
Chronic Myeloid Leukemia Treatments
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