Successful desensitization under antihistamine suppression in a case with urticaria due to osimertinib

J Oncol Pharm Pract. 2022 Sep;28(6):1454-1457. doi: 10.1177/10781552221075809. Epub 2022 Jan 21.

Abstract

Introduction: Osimertinib is an approved therapy for patients with a Thr790met (T790M) mutation diagnosed with non-small cell lung cancer (NSCLC) that progresses during epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI) therapy. However, in 7-13% of patients, drug-related side effects lead to discontinuation of osimertinib treatment. In such cases, osimertinib desensitization is a treatment option that can be considered.

Case report: A 59-year-old female patient, who was followed up with the diagnosis of stage 4 NSCLC, was consulted to the allergy clinic because of urticaria. The patient developed urticaria plaques 20 h after the third dose of osimertinib tablet.

Management & outcome: With the diagnosis of osimertinib-induced urticaria, desensitization was planned for the patient. Treatment was started with a dose of 0.1 mg/day osimertinib. The procedure was completed in approximately 50 days, and a dose of 80 mg/day was reached with antihistamine suppression.

Discussion: Here, a successful osimertinib desensitization in a patient with a history of osimertinib-related type 1 allergic reaction is reported. Osimertinib desensitization is a treatment option that should be considered in cases where treatment has to be ceased due to drug-related side effects.

Keywords: Osimertinib; allergy; cancer; desensitization; drug; immunotherapy; urticaria.

Publication types

  • Case Reports

MeSH terms

  • Acrylamides
  • Aniline Compounds / adverse effects
  • Antineoplastic Agents* / adverse effects
  • Carcinoma, Non-Small-Cell Lung* / drug therapy
  • Carcinoma, Non-Small-Cell Lung* / genetics
  • ErbB Receptors / genetics
  • Female
  • Histamine Antagonists / therapeutic use
  • Histamine H1 Antagonists / therapeutic use
  • Humans
  • Indoles
  • Lung Neoplasms* / drug therapy
  • Lung Neoplasms* / genetics
  • Middle Aged
  • Mutation
  • Protein Kinase Inhibitors / adverse effects
  • Pyrimidines
  • Urticaria* / chemically induced

Substances

  • Acrylamides
  • Aniline Compounds
  • Antineoplastic Agents
  • Histamine Antagonists
  • Histamine H1 Antagonists
  • Indoles
  • Protein Kinase Inhibitors
  • Pyrimidines
  • osimertinib
  • ErbB Receptors