Two cases of advanced melanoma with <scp>BRAF L597</scp> mutation: Options for systemic treatment

The combination of BRAF and MEK kinase inhibitors is a well-established treatment for BRAF V600-mutated advanced melanoma. However, the efficacy of these therapies against less common BRAF mutations, such as BRAF L597, remains unclear. We report two cases of advanced melanoma harboring the BRAF L597 mutation. In the first case, a 77-year-old man with metastatic melanoma achieved complete remission following combination therapy with nivolumab and ipilimumab. In the second case, a 50-year-old woman with metastatic melanoma exhibited resistance to multiple systemic therapies, including nivolumab, ipilimumab, and targeted therapy with encorafenib and binimetinib. These cases highlight the variable therapeutic responses in melanoma with the BRAF L597 mutation, suggesting that immune checkpoint inhibitors may be a viable first-line treatment, particularly for patients with a high tumor mutational burden. Further studies are needed to establish optimal treatment strategies for this rare mutation.

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Publication Details

Journal
The Journal of Dermatology
Published
2025-03-25
DOI
https://doi.org/10.1111/1346-8138.17718
Primary Topic
Melanoma and MAPK Pathways
Type
article
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article

Two cases of advanced melanoma with BRAF L597 mutation: Options for systemic treatment

Manami Takahashi, Yoshihide Asano, Ryo Amagai, Taku Fujimura et al.
1 links
The Journal of Dermatology
Melanoma and MAPK Pathways
article

Two cases of advanced melanoma with BRAF L597 mutation: Options for systemic treatment

Manami Takahashi, Yoshihide Asano, Ryo Amagai, Taku Fujimura, Yusuke Muto, Yumi Kambayashi, Kenta Oka, Erika Tamabuchi, Emi Yamazaki, Akira Hashimoto
article en

Abstract

The combination of BRAF and MEK kinase inhibitors is a well-established treatment for BRAF V600-mutated advanced melanoma. However, the efficacy of these therapies against less common BRAF mutations, such as BRAF L597, remains unclear. We report two cases of advanced melanoma harboring the BRAF L597 mutation. In the first case, a 77-year-old man with metastatic melanoma achieved complete remission following combination therapy with nivolumab and ipilimumab. In the second case, a 50-year-old woman with metastatic melanoma exhibited resistance to multiple systemic therapies, including nivolumab, ipilimumab, and targeted therapy with encorafenib and binimetinib. These cases highlight the variable therapeutic responses in melanoma with the BRAF L597 mutation, suggesting that immune checkpoint inhibitors may be a viable first-line treatment, particularly for patients with a high tumor mutational burden. Further studies are needed to establish optimal treatment strategies for this rare mutation.

The Journal of DermatologyVol. 52(6)
Tohoku University (JP)
Good health and well-being
Openalex Percentile: Top 95%
Melanoma and MAPK Pathways
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