Case Report: A patient with the rare third-generation TKI-resistant mutation EGFR L718Q who responded to afatinib plus cetuximab combination therapy
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Updated: Aug 21, 2025

Establishment and Characterization of Three Afatinib-resistant Lung Adenocarcinoma PC-9 Cell Lines Developed with Increasing Doses of Afatinib
Published on: June 26, 2019
Guoqing Zhang1, Beibei Yan1, Yanan Guo1
1Department of Thoracic Surgery and Lung Transplantation, First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China.
Abstract:
Third-generation tyrosine kinase inhibitors (TKIs), such as osimertinib, almonertinib and furmonertinib, overcome the mechanisms of resistance to first-generation inhibitors (such as gefitinib, erlotinib and icotinib) by incorporating an acrylamide group that alkylates the Cys797 of EGFR T790M. However, drug resistance is inevitable, even for third-generation TKIs. Screening for drug-resistant mutations by repeat biopsy and repeat gene sequencing is necessary after TKI treatment. Among various third-generation TKI-resistant mutations, secondary mutation of the L718 residue of EGFR exon 18 was found in approximately 8% of patients and is responsible for drug resistance in vitro and in vivo. Furthermore, there is limited clinical experience of targeted therapy for this mutation. Herein, we report for the first time that afatinib and cetuximab combination therapy can overcome such drug resistance.
Insights
Third-generation tyrosine kinase inhibitors (TKIs) face resistance, including EGFR exon 18 mutations. Afatinib and cetuximab combination therapy shows promise in overcoming this specific drug resistance.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Third-generation tyrosine kinase inhibitors (TKIs) target EGFR T790M mutations but are subject to acquired resistance.
- Resistance to TKIs, including third-generation agents, necessitates ongoing monitoring and development of new therapeutic strategies.
- Secondary mutations in EGFR exon 18, specifically at the L718 residue, represent a significant mechanism of resistance to third-generation TKIs in approximately 8% of patients.
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