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.

Frontiers in Oncology
|June 17, 2022
PubMed

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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