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Treatment Approaches for EGFR-Mutated Lung Cancers

A special issue of International Journal of Molecular Sciences (ISSN 1422-0067). This special issue belongs to the section "Molecular Oncology".

Deadline for manuscript submissions: 30 September 2026 | Viewed by 54

Special Issue Editor


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Guest Editor
Department of Medicine, Faculty of Medicine, Chiang Mai University, Chiang Mai, Thailand
Interests: lung cancer; common cancer; palliative care

Special Issue Information

Dear Colleagues,

Targeting EGFR (epidermal growth factor receptor)-mutated lung cancer represents a major paradigm shift in the management of non-small-cell lung cancer (NSCLC), transitioning from conventional cytotoxic chemotherapy to precision-based targeted therapy. This transformation has significantly improved clinical outcomes and ushered in a new therapeutic era.

The role of EGFR tyrosine kinase inhibitors (TKIs) has expanded from metastatic and unresectable disease to resected early-stage NSCLC in the adjuvant setting, marking an important milestone in precision oncology. To further enhance efficacy and overcome resistance, combination strategies have been explored. EGFR–MET bispecific antibodies and anti-angiogenic therapies have demonstrated promising clinical benefit, particularly in resistant settings.

In patients with brain metastases, the combination of Osimertinib and chemotherapy has shown significant improvements in response rates, progression-free survival (PFS) and overall survival (OS).

Although immunotherapy has historically demonstrated limited efficacy in EGFR-mutated NSCLC, recent studies suggest that combining immunotherapy with chemotherapy and/or anti-angiogenic agents may improve outcomes after progression on prior EGFR TKI therapy.

Resistance to EGFR TKIs remains inevitable and involves multiple mechanisms, including EGFR-dependent alterations (T790M, C797S and amplification), EGFR-independent pathways (MET and HER2/3 amplification, downstream signaling and AXL activation) and phenotypic transformation such as small-cell lung cancer and epithelial–mesenchymal transition. Molecular reassessment through re-biopsy or liquid biopsy is essential to guide subsequent treatment.

Circulating tumor DNA (ctDNA) is an emerging tool for detecting minimal residual disease, guiding therapy and predicting survival.

This Special Issue highlights current and emerging strategies to improve outcomes in EGFR-mutated lung cancer.

Dr. Busyamas Chewaskulyong
Guest Editor

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Keywords

  • NSCLC
  • EGFR TKIs
  • osimertinib
  • chemotherapy
  • EGFR–MET bispecific antibodies
  • immunotherapy
  • anti-angiogenesis
  • resistance mechanisms
  • ctDNA
  • brain metastases

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