An EGFR-mutated Lung Adenocarcinoma Undergoing Squamous Cell Carcinoma Transformation Exhibited a Durable Response to
Mitsuo Sato1, Akira Matsui1, Yoshie Shimoyama2
1Department of Respiratory Medicine, Nagoya University Graduate School of Medicine, Japan.
Abstract:
Squamous cell carcinoma (SCC) transformation has been identified as a mechanism of resistance to first-generation epidermal growth factor receptor tyrosine kinase inhibitors (EGFR-TKIs), gefitinib or erlotinib, in EGFR-mutated lung cancer. However, whether second- or third-generation TKIs can overcome resistance due to SCC transformation remains unclear. We herein report an EGFR-mutated lung adenocarcinoma undergoing transformation into SCC that exhibited a durable response to afatinib, which is a second-generation irreversible EGFR-TKI. We suggest that afatinib can be considered as a treatment option for EGFR-mutated tumor undergoing SCC transformation, particularly in the absence of a T790M mutation.
Insights
Squamous cell carcinoma transformation can cause resistance to EGFR-TKIs in lung cancer. Afatinib, a second-generation TKI, showed a durable response in an EGFR-mutated lung adenocarcinoma undergoing this transformation.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- First-generation EGFR-TKIs (gefitinib, erlotinib) face resistance via squamous cell carcinoma (SCC) transformation in EGFR-mutated lung cancer.
- The efficacy of newer-generation TKIs against SCC transformation is not well-established.
Observation:
- A case of EGFR-mutated lung adenocarcinoma is presented.
- This tumor underwent transformation into squamous cell carcinoma.
Findings:
- The transformed tumor exhibited a sustained response to afatinib, a second-generation irreversible EGFR-TKI.
- This response occurred despite the SCC transformation, a known resistance mechanism.
Implications:
- Afatinib may be a viable treatment option for EGFR-mutated lung tumors that transform into SCC.
- This is particularly relevant when the T790M resistance mutation is absent.
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