Afatinib-associated Stevens-Johnson syndrome in an EGFR-mutated lung cancer patient

Janine Doesch1, Dirk Debus2, Christian Meyer3

  • 1Department of Respiratory Medicine, Allergology and Sleep Medicine, Paracelsus Medical University, General Hospital Nuernberg, Nuremberg, Germany.

Abstract

Insights

Afatinib, a treatment for EGFR-mutated non-small-cell lung cancer, can cause Stevens-Johnson syndrome (SJS). Early recognition and discontinuation of afatinib with glucocorticoids can lead to recovery.

Area of Science:

  • Oncology
  • Dermatology
  • Pharmacology

Background:

  • Afatinib is an approved epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor (TKI) for advanced non-small-cell lung cancer (NSCLC) with EGFR mutations.
  • Stevens-Johnson syndrome (SJS) is a rare but severe adverse event associated with EGFR-directed TKIs.

Observation:

  • A case report details a 79-year-old female with metastatic EGFR-mutated NSCLC who developed SJS after two months of first-line afatinib treatment.
  • The patient presented with severe cutaneous adverse drug reactions involving skin and mucous membranes.

Findings:

  • Discontinuation of afatinib was initiated upon SJS diagnosis.
  • Systemic glucocorticoid therapy was administered concurrently with afatinib cessation.

Implications:

  • This case highlights the importance of recognizing SJS as a potential adverse reaction to afatinib in NSCLC patients.
  • Prompt identification and appropriate management, including TKI discontinuation and glucocorticoid use, are crucial for patient recovery and improved outcomes.

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