Volume 52, Issue 6 pp. 1090-1093
CONCISE COMMUNICATION

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

Ryo Amagai

Ryo Amagai

Department of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan

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Taku Fujimura

Corresponding Author

Taku Fujimura

Department of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan

Correspondence

Taku Fujimura, Department of Dermatology, Tohoku University Graduate School of Medicine, 1-1 Seiryo-machi, Aoba-ku, Sendai, Miyagi 980-8574, Japan.

Email: [email protected]

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Yumi Kambayashi

Yumi Kambayashi

Department of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan

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Manami Takahashi-Watanabe

Manami Takahashi-Watanabe

Department of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan

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Emi Yamazaki

Emi Yamazaki

Department of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan

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Erika Tamabuchi

Erika Tamabuchi

Department of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan

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Kenta Oka

Kenta Oka

Department of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan

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Yusuke Muto

Yusuke Muto

Department of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan

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Akira Hashimoto

Akira Hashimoto

Department of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan

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Yoshihide Asano

Yoshihide Asano

Department of Dermatology, Tohoku University Graduate School of Medicine, Sendai, Japan

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First published: 25 March 2025

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.

CONFLICT OF INTEREST STATEMENT

None declared.

DATA AVAILABILITY STATEMENT

All data generated or analyzed during this study are included in this article. Further inquiries can be directed to the corresponding author.

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