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Updated: Mar 23, 2026

Establishment and Characterization of Three Afatinib-resistant Lung Adenocarcinoma PC-9 Cell Lines Developed with Increasing Doses of Afatinib
Published on: June 26, 2019
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.
Introduction:
Afatinib is a tyrosine kinase inhibitor (TKI), that has been approved for treating patients with epidermal growth factor receptor (EGFR) mutated advanced non-small-cell lung cancer (NSCLC). Stevens-Johnson syndrome (SJS) related to EGFR directed TKIs is a rare adverse event.
Case Presentation:
We report a case of a 79-year-old white female with EGFR-mutated, metastatic non-small-cell lung cancer treated with afatinib as first-line palliative treatment, who developed a SJS after two months of treatment. Discontinuation of the TKI and systemic glucocorticoid treatment led to improvement of symptoms and recovery.
Conclusion:
Severe adverse cutaneous drug reactions that predominantly involve the skin and mucous membranes during treatment with afatinib should alert clinicians to suspect SJS and react appropriately.
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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