Osimertinib-induced Keratitis and Secondary Toxic Epidermal Necrotic Drug Eruption- A Case Report and Literature Review

Curr Drug Saf. 2024;19(2):309-312. doi: 10.2174/1574886318666230529123200.

Abstract

Background: Osimertinib is a third-generation Tyrosine Kinase inhibitor, mainly used in non-small cell lung cancer with EGFR mutation. Its efficacy and safety have been confirmed by clinical practice. Toxic epidermolysis necrotizing disease (TEN) is a severe drug eruption that is rare in clinics and has a high mortality rate. Toxic epidermal necrotic drug rash caused by Osimeritinib is even rarer.

Objective: To investigate the rare side effects of Osimertinib through a case of toxic Epidermal necrosis.

Case presentation: A 63-year-old female patient was diagnosed with lung adenocarcinoma with brain metastases, and genetic testing revealed an EGFR21 exon mutation. The disease progressed 24 days after the administration of gefitinib, then the patient switched to Osimertinib (80 mg QD) and, resulting in keratitis and secondary systemic toxic epidermolysis necrotizing disease (TEN). Finally, the patient died.

Conclusion: Although the clinical use of osimertinib is becoming widespread, the side effects may not be fully understood. Clinicians should pay more attention to the occurrence of the side reaction and deal with it in time.

Keywords: EGFR; Osimertinib; SJS/TEN; keratitis; oncology.; target-therapy.

Publication types

  • Review
  • Case Reports

MeSH terms

  • Antineoplastic Agents* / adverse effects
  • Carcinoma, Non-Small-Cell Lung* / drug therapy
  • Drug Eruptions*
  • ErbB Receptors / genetics
  • ErbB Receptors / therapeutic use
  • Female
  • Humans
  • Lung Neoplasms* / drug therapy
  • Lung Neoplasms* / genetics
  • Middle Aged
  • Necrosis / chemically induced
  • Necrosis / drug therapy
  • Pharmaceutical Preparations
  • Protein Kinase Inhibitors / adverse effects
  • Skin Diseases* / drug therapy

Substances

  • osimertinib
  • Pharmaceutical Preparations
  • Antineoplastic Agents
  • ErbB Receptors
  • Protein Kinase Inhibitors