Osimertinib-Associated Toxic Epidermal Necrolysis in a Lung Cancer Patient Harboring an EGFR Mutation-A Case Report and a Review of the Literature

Medicina (Kaunas). 2020 Aug 11;56(8):403. doi: 10.3390/medicina56080403.

Abstract

Toxic epidermal necrolysis (TEN) and Stevens-Johnson syndrome (SJS) are life-threatening dermatologic adverse events in the same category, caused by a delayed-type drug hypersensitivity reaction. Although skin toxicity is common during treatment with epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs), osimertinib-associated TEN is quite rare-thus far, only one report has been published from China. We report a case of an 80-year-old Japanese woman with lung adenocarcinoma harboring an EGFR-sensitizing mutation who was treated with osimertinib as the first-line treatment. Forty-six days after osimertinib induction, diffuse erythematous rash rapidly spread over the patient's trunk along with vesicles and purpuric macules; furthermore, she developed targetoid erythema on the face. Despite osimertinib discontinuation and corticosteroid treatment, diffuse erythema with Nikolsky's sign, general epidermal detachment, erosion and loose blisters developed over her entire body including the face. Based on her symptoms, TEN was diagnosed and thus, intravenous immunoglobulin was immediately administered for 4 days. The treatment ameliorated TEN-associated skin toxicity and caused epithelialization. Reports on osimertinib-associated SJS/TEN are scarce and only one report each on SJS and TEN from China is available. This is the first report of osimertinib-associated TEN from Japan. Cases of EGFR-TKI-associated SJS/TEN have been reported predominantly from Asian countries, suggesting ethnicity and genetic linkage play a role in the underlying mechanism.

Keywords: EGFR tyrosine kinase inhibitor; ethnicity; non-small-cell lung cancer; osimertinib; toxic epidermal necrolysis.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Acrylamides / adverse effects*
  • Adenocarcinoma / drug therapy
  • Adenocarcinoma / genetics*
  • Aged, 80 and over
  • Aniline Compounds / adverse effects*
  • Antineoplastic Agents / adverse effects*
  • Asian People / genetics
  • ErbB Receptors / genetics
  • Female
  • Humans
  • Immunoglobulins, Intravenous / therapeutic use
  • Lung Neoplasms / drug therapy
  • Lung Neoplasms / genetics*
  • Mutation
  • Protein Kinase Inhibitors / adverse effects*
  • Stevens-Johnson Syndrome / drug therapy
  • Stevens-Johnson Syndrome / ethnology
  • Stevens-Johnson Syndrome / etiology*
  • Stevens-Johnson Syndrome / pathology

Substances

  • Acrylamides
  • Aniline Compounds
  • Antineoplastic Agents
  • Immunoglobulins, Intravenous
  • Protein Kinase Inhibitors
  • osimertinib
  • EGFR protein, human
  • ErbB Receptors