Volume 47, Issue 10 p. 1191-1194
Concise Communication

Frequent brain metastases during treatment with BRAF/MEK inhibitors: A retrospective single institutional study

Yoshiyuki Nakamura

Corresponding Author

Department of Dermatology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan

Correspondence: Yoshiyuki Nakamura, M.D., Ph.D., Department of Dermatology, Faculty of Medicine, University of Tsukuba, 1‐1‐1 Tennodai, Tsukuba, Ibaraki 305‐8575, Japan. Email: ynakamura-tuk@umin.ac.jp

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Yosuke Ishitsuka

Department of Dermatology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan

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Ryota Tanaka

Department of Dermatology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan

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Naoko Okiyama

Department of Dermatology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan

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Rei Watanabe

Department of Dermatology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan

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Akimasa Saito

Department of Dermatology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan

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Junichi Furuta

Department of Dermatology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan

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Yasuhiro Fujisawa

Department of Dermatology, Faculty of Medicine, University of Tsukuba, Tsukuba, Japan

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First published: 29 June 2020
Citations: 1

Abstract

Recent clinical trials revealed that both immune checkpoint inhibitors (ICI) and BRAF/MEK inhibitors significantly prolonged survival in melanoma patients when used for both advanced stage disease and postoperative adjuvant therapy. Although BRAF/MEK inhibitors are associated with a higher objective response rate than ICI, most patients relapse during treatment. However, progression patterns during treatment with BRAF/MEK inhibitors have not been extensively investigated. Here, we retrospectively collected the data of melanoma patients initially treated with BRAF/MEK inhibitors or anti‐programmed death 1 (PD‐1) antibody monotherapy at the University of Tsukuba Hospital and compared their results. The χ2‐test revealed that frequency of brain metastasis (BM) development was significantly higher in cases treated with BRAF/MEK inhibitors compared with those with anti‐PD‐1 antibody monotherapy. In addition, BM‐free survival in cases treated with BRAF/MEK inhibitors was significantly shorter than those treated with anti‐PD‐1 antibody monotherapy. Our results indicate that BM development during treatment with BRAF/MEK inhibitors may be more frequent than anti‐PD‐1 antibody monotherapy, even though the extracranial metastases are well controlled. Therefore, we recommend frequent brain examinations during treatment with BRAF/MEK inhibitors to detect BM at an early stage and to promptly administrate ICI with local radiation therapy.

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