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Personalized Therapy in a Patient With EGFR-Mutated NSCLC Developing Sequential CCDC6-RET Fusion and BRAF V600E
Arianna Marinello1,2, Claudia Parisi1,3, Damien Vasseur4
1Department of Medical Oncology, International Center for Thoracic Cancers (CICT), Gustave Roussy, Villejuif, France.
Abstract:
In this case report, we describe a case of sequential acquired CCDC6 -RET fusion and BRAF V600E mutation observed in a patient with EGFR-mutated NSCLC treated with osimertinib and with combined selpercatinib and osimertinib. The discovery of genomic resistance mechanisms was facilitated by serial liquid and tissue biopsies and molecular tumor board discussion. After the identification of CCDC6-RET fusion, the patient received a combination of selpercatinib and osimertinib with prolonged benefit and manageable toxicity. When a novel BRAF V600E mutation was detected at progression, the molecular tumor board suggested the administration of triple therapy, adding trametinib (anti-MEK). Nevertheless, treatment was discontinued for toxicity, highlighting the challenges of using multiple drug combinations to address complex resistance.
Insights
This case report details acquired resistance mechanisms in EGFR-mutated NSCLC. Sequential CCDC6-RET fusion and BRAF V600E mutations emerged during targeted therapy, posing treatment challenges.
Area of Science:
- Oncology
- Genomics
- Pharmacology
Background:
- Non-small cell lung cancer (NSCLC) with EGFR mutations often develops resistance to targeted therapies.
- Understanding acquired resistance mechanisms is crucial for optimizing treatment strategies.
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