Abstract
We present a patient with metastatic NSCLC harboring a compound EGFR mutation with co-occurring G719A and T790M mutation. T790M mutation was treatment emergent mutation when patient was on early generation tyrosine kinase inhibitors. Initial Guardant 360 showed that G719A was the dominant clone. Following, osimertinib, the patient had only a radiographic disease stabilization and then developed both clinical and radiographic progression. On progression, T790M was undetectable but G719A continued to be the dominant clone. Subsequent administration of afatinib led to a clinical and radiological response. To our knowledge, this is the first case report describing co-occurrence of EGFR G719A and T790M mutations and the clonal evolution during treatment with anti-EGFR therapies.
Original language | English (US) |
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Article number | LMT54 |
Journal | Lung Cancer Management |
Volume | 11 |
Issue number | 1 |
DOIs | |
State | Published - Mar 1 2022 |
Bibliographical note
Publisher Copyright:© 2022 Amit A Kulkarni.
Keywords
- afatinib
- compound mutations
- EGFR mutation
- liquid biopsy
- mutations
- next-generation sequencing
- NSCLC
- osimertinib
- rare mutations
- uncommon tyrosine kinase inhibitors
PubMed: MeSH publication types
- Case Reports