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Published on: July 21, 2018
Effective Treatment of Lung Adenocarcinoma With a Novel SLC44A1-BRAF Fusion Using Pembrolizumab Followed by
Sho Yasui1, Takayuki Honda1, Iichiro Onishi2
1Department of Respiratory Medicine, Tokyo Medical and Dental University, Tokyo, JPN.
Abstract:
The serine-threonine protein kinase B-RAF (BRAF) fusions are rarely observed in non-small cell lung cancer (NSCLC) accounting for less than 1%, and therapeutic evidence for molecular-targeted drugs is lacking, unlike for BRAF V600E mutation by RAF and MEK inhibitors. A 75-year-old female patient with no smoking history and mild renal dysfunction developed recurrent lung adenocarcinoma and was initially treated with pembrolizumab immunotherapy followed by chemotherapy using docetaxel showing a certain efficacy but the disease finally progressed. Comprehensive genome profiling showed a novel SLC44A1-BRAF fusion and the tumor progression was controlled with the MEK inhibitor trametinib. Because of the rarity of NSCLC with BRAF fusion, the description of this case would be helpful for the treatment strategy for such tumors.
Insights
A rare BRAF fusion in non-small cell lung cancer (NSCLC) was identified in a patient. Treatment with a MEK inhibitor effectively controlled tumor progression, offering a potential therapeutic strategy.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- BRAF fusions are rare oncogenic drivers in non-small cell lung cancer (NSCLC), occurring in less than 1% of cases.
- Limited therapeutic options and evidence exist for BRAF fusion-positive NSCLC, unlike for BRAF V600E mutations.
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