Life threatening hepatotoxicity induced by Nilotinib

J Oncol Pharm Pract. 2023 Mar;29(2):465-468. doi: 10.1177/10781552221102588. Epub 2022 Jun 1.

Abstract

Introduction: Tyrosine kinase inhibitor had changed the prognosis of chronic myeloid leukemia (CML) and the overall survival had reached 95%. Unfortunately, adverse events (AEs) remain an obstacle to following successful treatment in CML impairing the quality of life and sometimes endangering the lives of patients. To this end, we show this clinical case to discuss strategies to deal with rare AEs in a way to preserve the patient's life and to maintain not only a good response to treatment but also confidence and compliance of the patient.

Case report: We report the case of a 57-year-old woman diagnosed with CML at the chronic phase who developed rare life-threatening hepatotoxicity (major cytolysis and prothrombin time fall) secondary to Nilotinib used as second-line treatment. This complication settled despite an optimal molecular response.

Management and outcome: We discuss below the follow-up and management in our center and according to the literature with more sophisticated pharmacological methods.

Discussion: Although we used to monitor disease molecular response to treatment, we need solutions and manuscripts for monitoring drug dose parameters to avoid unusual dangerous effects risking the patient life. We conclude that monitoring the disease as well as the treatment pharmacokinetics is mandatory to better carry on CML patients.

Keywords: Ehronic myeloid leukemia; Nilotinib; case report; hepatotoxicity.

Publication types

  • Case Reports

MeSH terms

  • Antineoplastic Agents* / adverse effects
  • Chemical and Drug Induced Liver Injury* / drug therapy
  • Chemical and Drug Induced Liver Injury* / etiology
  • Female
  • Humans
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive* / diagnosis
  • Leukemia, Myelogenous, Chronic, BCR-ABL Positive* / drug therapy
  • Middle Aged
  • Protein Kinase Inhibitors / adverse effects
  • Pyrimidines / adverse effects
  • Quality of Life
  • Treatment Outcome

Substances

  • Antineoplastic Agents
  • Pyrimidines
  • Protein Kinase Inhibitors