CDK 4/6 inhibitor successful rechallenge after limiting hepatic toxicity

Breast J. 2020 Feb;26(2):255-257. doi: 10.1111/tbj.13532. Epub 2019 Sep 8.

Abstract

A 59-year-old woman presented with a bone-only metastatic luminal breast cancer. She received first-line treatment with aromatase inhibitors associated with a cyclin-dependent kinase (CDK) 4/6 inhibitor, ribociclib. She developed Grade 3 elevated transaminases leading us to interrupt ribociclib permanently. Specific toxicity of the CDK 4/6 inhibitor ribociclib was retained. Once transaminase levels normalized, the patient initiated another CDK4/6 inhibitor, palbociclib, using an escalating dose without reappearance of hepatic injury. This case suggests the possibility of rechallenge after hepatic toxicity with a different CDK 4/6 inhibitor using dose escalation and careful monitoring.

Keywords: CDK 4/6 inhibitor; elevated transaminase; hepatic toxicity; luminal breast cancer; rechallenge.

Publication types

  • Case Reports

MeSH terms

  • Alanine Transaminase / blood
  • Aminopyridines / adverse effects*
  • Aromatase Inhibitors / therapeutic use
  • Aspartate Aminotransferases / blood
  • Bone Neoplasms / drug therapy*
  • Bone Neoplasms / secondary
  • Breast Neoplasms / pathology*
  • Carcinoma, Lobular / drug therapy*
  • Carcinoma, Lobular / secondary
  • Chemical and Drug Induced Liver Injury / blood
  • Chemical and Drug Induced Liver Injury / etiology*
  • Cyclin-Dependent Kinase 4 / antagonists & inhibitors
  • Cyclin-Dependent Kinase 6 / antagonists & inhibitors
  • Drug Substitution
  • Drug Therapy, Combination
  • Female
  • Humans
  • Letrozole / therapeutic use
  • Middle Aged
  • Piperazines / therapeutic use*
  • Protein Kinase Inhibitors / adverse effects*
  • Protein Kinase Inhibitors / therapeutic use
  • Purines / adverse effects*
  • Pyridines / therapeutic use*

Substances

  • Aminopyridines
  • Aromatase Inhibitors
  • Piperazines
  • Protein Kinase Inhibitors
  • Purines
  • Pyridines
  • Letrozole
  • Aspartate Aminotransferases
  • Alanine Transaminase
  • Cyclin-Dependent Kinase 4
  • Cyclin-Dependent Kinase 6
  • palbociclib
  • ribociclib