PD-L1-negative non-small cell lung cancer harbouring a rare BRAF mutation with successful treatment of first-line pembrolizumab plus chemotherapy: A case report and review the literature.
Kien Hung DoTai Van NguyenPhuong Nguyen Thi BichGia Hoang NguyenVan Chu NguyenPublished in: Respirology case reports (2023)
BRAF mutations are uncommon in non-small cell lung cancer (NSCLC), accounting for less than 5% of all NSCLC cases. The utilization of targeted therapies in non-V600E BRAF mutant NSCLC is considered controversial, although non-V600E genotype is reported in ~50% of all BRAF mutant patients. We document the case of a 63-year-old patient with NSCLC harbouring a rare BRAF E501Q mutation, who had prolonged response to immunotherapy combined with chemotherapy in Vietnam. The patient was diagnosed with metastatic PD-L1-negative lung adenocarcinoma and received pembrolizumab plus chemotherapy as first-line treatment. After completing 35 cycles of pembrolizumab and pemetrexed, his disease has remained stable during the treatment-free follow-up period, and he is alive 38 months after treatment initiation at the latest follow-up. Immune-based therapy is an appropriate option for lung adenocarcinoma with rare non-V600E BRAF mutation. Further clinical studies are necessary to determine the effectiveness of using immune-based therapy in this specific population.
Keyphrases
- advanced non small cell lung cancer
- small cell lung cancer
- wild type
- metastatic colorectal cancer
- epidermal growth factor receptor
- systematic review
- locally advanced
- squamous cell carcinoma
- ejection fraction
- randomized controlled trial
- end stage renal disease
- brain metastases
- case report
- newly diagnosed
- chronic kidney disease
- prognostic factors
- radiation therapy
- stem cells
- cell therapy
- peritoneal dialysis
- replacement therapy