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病例报告:成功使用MEK抑制剂作为辅助方法治疗儿科MAP4-RAF1融合阳性实体瘤。

Case report: Successful use of MEK inhibitors as an adjuvant approach in the treatment of pediatric MAP4-RAF1 fusion-positive solid tumor.

作者信息

Yang Shen, Zhang Shixuan, Wang Jiarong, Zhang Nan, Wang Jinhu, Jiang Mawei, Meng Deguang, Xie Jinrong, Chang Xiaofeng, Cheng Haiyan, Wang Huanmin

机构信息

Department of Oncology Surgery, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing, 100045, China.

Research and Innovation Center, Shanghai Pudong Hospital, Fudan University, Shanghai, 201203, China.

出版信息

NPJ Precis Oncol. 2025 Jun 21;9(1):201. doi: 10.1038/s41698-025-00996-5.

Abstract

RAF protein kinase acts downstream of RAS in the MAPK pathway, and mutations in the RAF family protein BRAF are frequently observed in adult tumours, with MEK inhibitors proving effective in treatment. However, RAF family protein RAF1 fusions are rare, particularly in pediatric soft tissue tumors, and the efficacy of targeted therapies remains uncertain. This study presents a rare case of a MAP4-RAF1 fusion-positive solid tumor in a child, unresponsive to conventional chemotherapy, surgery, second-line chemotherapy, and sorafenib-targeted therapy. Protein structure simulations predicted trametinib to exhibit optimal efficacy among MEK inhibitors in structural modelling, and it then demonstrated clinical effectiveness in this child. This study underscores the importance of molecular interaction simulations in precise drug screening for clinical decision-making and highlights MEK inhibitors' potential as adjunctive therapy for pediatric RAF1 fusion tumors.

摘要

RAF蛋白激酶在MAPK通路中作用于RAS下游,RAF家族蛋白BRAF的突变在成人肿瘤中经常被观察到,事实证明MEK抑制剂在治疗中有效。然而,RAF家族蛋白RAF1融合很少见,尤其是在儿童软组织肿瘤中,靶向治疗的疗效仍不确定。本研究报告了一例罕见的儿童MAP4-RAF1融合阳性实体瘤病例,该病例对传统化疗、手术、二线化疗和索拉非尼靶向治疗均无反应。蛋白质结构模拟预测曲美替尼在结构建模中在MEK抑制剂中表现出最佳疗效,随后在该儿童中证明了其临床有效性。本研究强调了分子相互作用模拟在精确药物筛选以用于临床决策中的重要性,并突出了MEK抑制剂作为儿童RAF1融合肿瘤辅助治疗的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e5e3/12182580/34f97f770a1b/41698_2025_996_Fig1_HTML.jpg

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