# Effective Treatment of Lung Adenocarcinoma With a Novel SLC44A1-BRAF Fusion Using Pembrolizumab Followed by Trametinib: A Case Report

**Authors:** Sho Yasui, Takayuki Honda, Iichiro Onishi, Sadakatsu Ikeda, Yasunari Miyazaki

PMC · DOI: 10.7759/cureus.54739 · Cureus · 2024-02-23

## TL;DR

A 75-year-old woman with lung adenocarcinoma responded to treatment with pembrolizumab and trametinib after a rare SLC44A1-BRAF fusion was identified.

## Contribution

Reports a novel SLC44A1-BRAF fusion in lung cancer and its effective treatment with MEK inhibition.

## Key findings

- SLC44A1-BRAF fusion was identified in a lung adenocarcinoma patient.
- Trametinib controlled tumor progression after disease progression on pembrolizumab and docetaxel.
- The case highlights potential treatment strategies for rare BRAF fusion-positive NSCLC.

## 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.

## Linked entities

- **Genes:** SLC44A1 (solute carrier family 44 member 1) [NCBI Gene 23446], BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673]
- **Proteins:** BRAF (B-Raf proto-oncogene, serine/threonine kinase)
- **Chemicals:** trametinib (PubChem CID 11707110), docetaxel (PubChem CID 148124)
- **Diseases:** lung adenocarcinoma (MONDO:0005061), non-small cell lung cancer (MONDO:0005233), NSCLC (MONDO:0005233)

## Full-text entities

- **Genes:** SIK1 (salt inducible kinase 1) [NCBI Gene 150094] {aka DEE30, MSK, SIK, SIK-1, SIK1B, SNF1LK}, ZHX2 (zinc fingers and homeoboxes 2) [NCBI Gene 22882] {aka AFR1, RAF}, BRAF (B-Raf proto-oncogene, serine/threonine kinase) [NCBI Gene 673] {aka B-RAF1, B-raf, BRAF-1, BRAF1, NS7, RAFB1}, MAP2K7 (mitogen-activated protein kinase kinase 7) [NCBI Gene 5609] {aka JNKK2, MAPKK7, MEK, MEK 7, MKK7, PRKMK7}, SLC44A1 (solute carrier family 44 member 1) [NCBI Gene 23446] {aka CD92, CDW92, CHTL1, CONATOC, CTL1}
- **Diseases:** tumor (MESH:D009369), NSCLC (MESH:D002289), Lung Adenocarcinoma (MESH:D000077192), renal dysfunction (MESH:D007674)
- **Species:** Homo sapiens (human, species) [taxon 9606]
- **Mutations:** V600E

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC10960948/full.md

## References

17 references — full list in the complete paper: https://tomesphere.com/paper/PMC10960948/full.md

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Source: https://tomesphere.com/paper/PMC10960948