Alectinib induces marked red cell spheroacanthocytosis in a near-ubiquitous fashion and is associated with reduced eosin-5-maleimide binding

Pathology. 2021 Aug;53(5):608-612. doi: 10.1016/j.pathol.2020.10.023. Epub 2021 Feb 19.

Abstract

We reviewed haematological investigations for 43 patients treated at a single centre with alectinib, an inhibitor of anaplastic lymphoma kinase (ALK) which is considered standard first-line treatment for patients with ALK-rearranged advanced non-small cell lung cancer. Ninety-five percent of patients developed marked acanthocytosis, echinocytosis and/or spheroacanthocytosis, not observable with prior treatment with other ALK-inhibitors. Anaemia developed in 73% of patients (38% <100 g/L, 8% <80 g/L), though definite new haemolysis was present in only 11%. Eosin-5-maleimide binding was reduced in all assessed patients, and increased membrane cholesterol was identified in one patient assessed with lattice light sheet microscopy. We have identified a previously undescribed phenomenon whereby alectinib induces red cell membrane abnormalities in nearly all patients through an unclear, but likely ALK-independent, mechanism, resulting in mild anaemia without universal haemolysis.

Keywords: Alectinib; acanthocytosis; eosin-5-maleimide; spherocytosis.

MeSH terms

  • Abetalipoproteinemia / chemically induced
  • Abetalipoproteinemia / pathology*
  • Anaplastic Lymphoma Kinase / antagonists & inhibitors*
  • Anaplastic Lymphoma Kinase / metabolism
  • Anemia / chemically induced
  • Anemia / pathology
  • Carbazoles / adverse effects*
  • Carbazoles / metabolism
  • Carcinoma, Non-Small-Cell Lung / drug therapy
  • Carcinoma, Non-Small-Cell Lung / pathology*
  • Hemolysis / drug effects
  • Humans
  • Lung Neoplasms / drug therapy
  • Lung Neoplasms / pathology*
  • Maleimides / metabolism
  • Piperidines / adverse effects*
  • Piperidines / metabolism
  • Protein Kinase Inhibitors / adverse effects*
  • Protein Kinase Inhibitors / metabolism
  • Retrospective Studies

Substances

  • Carbazoles
  • Maleimides
  • Piperidines
  • Protein Kinase Inhibitors
  • ALK protein, human
  • Anaplastic Lymphoma Kinase
  • alectinib