Case Report: Afatinib Sensitivity in Rare EGFR E746_L747delinsIP Mutated LUAD With Peritoneal Metastases
Lili Zhang1,2, Lu Yang3, Binxu Sun1,2
1Department of Oncology, First Teaching Hospital of Tianjin University of Traditional Chinese Medicine, Tianjin, China.
Abstract:
Patients with non-small cell lung cancer harboring the epidermal growth factor receptor (EGFR)-sensitive mutations are known to benefit significantly from EGFR tyrosine kinase inhibitors (TKIs), such as erlotinib, gefitinib, icotinib, or afatinib. However, the efficacy of EGFR-TKIs against rare mutations has not yet been well investigated. Here, we report a female patient with advanced lung adenocarcinoma (LUAD), carrying a rare mutation of EGFR Exon19 E746_L747delinsIP, who was administered first-generation EGFR-TKIs as the first-line treatment. The patient continued to progress slowly until peritoneal metastases have occurred. Subsequently, the patient was treated with anlotinib for 5 months until disease progression. Given the finding of the same EGFR rare mutation in peritoneal effusion without other EGFR-TKI resistance mutations, the patient received afatinib with a tremendous response. Our results may be of clinical relevance for patients with LUAD carrying this rare mutation, and these findings warrant further investigation.
Insights
This study highlights a rare EGFR mutation in lung adenocarcinoma. Afatinib showed a significant response in a patient with this mutation, suggesting potential therapeutic value.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors (TKIs) are effective for non-small cell lung cancer (NSCLC) with common EGFR mutations.
- The efficacy of EGFR-TKIs against rare EGFR mutations remains largely uninvestigated.
Observation:
- A patient with advanced lung adenocarcinoma (LUAD) presented with a rare EGFR Exon19 E746_L747delinsIP mutation.
- Initial treatment with first-generation EGFR-TKIs resulted in slow progression and eventual peritoneal metastasis.
- Subsequent treatment with anlotinib led to disease progression.
Findings:
- The rare EGFR mutation was detected in peritoneal effusion without common resistance mutations.
- Afatinib treatment yielded a tremendous response in the patient with this rare mutation.
Implications:
- This case suggests afatinib may be a viable treatment option for LUAD patients with the rare EGFR Exon19 E746_L747delinsIP mutation.
- Further clinical investigation is warranted to confirm the efficacy of afatinib in similar cases.
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