Clinical and Pathologic Complete Response to Gefitinib in a Patient with SqCLC Harboring EGFR p.E746_S752delinsV

Weitao Zhuang1,2, Chao Zhang3, Yong Tang1

  • 1Department of Thoracic Surgery, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, 510080, People's Republic of China.

Oncotargets and Therapy
|September 23, 2021
PubMed

Insights

A rare EGFR mutation in advanced squamous cell lung cancer (SqCLC) responded completely to neoadjuvant gefitinib. This suggests EGFR testing benefits select SqCLC patients, particularly females and light smokers.

Area of Science:

  • Oncology
  • Molecular Biology
  • Genetics

Background:

  • Targeted therapy development for squamous cell lung cancer (SqCLC) faces challenges due to limited actionable mutations and predicting treatment efficacy.
  • Epidermal Growth Factor Receptor (EGFR) mutations are crucial targets in non-small cell lung cancer, but their role in SqCLC is less defined.

Observation:

  • A case of treatment-naïve stage IIIB SqCLC with a rare EGFR p.E746_S752delinsV mutation was identified.
  • The patient received neoadjuvant gefitinib, a first-generation EGFR tyrosine kinase inhibitor (TKI).

Findings:

  • The patient achieved a clinical complete response to neoadjuvant gefitinib.
  • Pathological complete response was confirmed post-surgical resection.
  • No disease recurrence was observed during a 20-month follow-up period.

Implications:

  • First-generation EGFR TKIs may be a viable neoadjuvant treatment option for advanced SqCLC patients with the specific EGFR p.E746_S752delinsV mutation.
  • EGFR mutation testing could offer clinical benefits for SqCLC patients, especially in specific demographics like females and never/former light smokers.

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