Leptomeningeal Dissemination in TERT Promoter-mutant Anaplastic Pleomorphic Xanthoastrocytoma Responding to BRAF-MEK Inhibition: A Case Report.

NMC case report journal Pub Date : 2026-08-14 eCollection Date: 2026-01-01 DOI:10.2176/jns-nmc.2026-0094
Ryota Kitano, Hiroaki Nagashima, Hiroki Goto, Shunsuke Yamanishi, Masamitsu Nishihara, Kazuhiro Tanaka, Yoshihiro Muragaki, Takashi Sasayama
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Abstract

Pleomorphic xanthoastrocytoma is a rare brain tumor that frequently harbors the oncogenic BRAF V600E mutation. Approximately 28.6%-47% of high-grade pleomorphic xanthoastrocytomas are associated with TERT promoter mutation and leptomeningeal dissemination, for which no established treatment exists and the prognosis remains poor. Combination therapy with BRAF and MEK inhibitors has demonstrated efficacy in BRAF V600E-mutant brain tumors. We report a case of a 22-year-old man with a right temporal lobe tumor initially diagnosed as World Health Organization grade 2 pleomorphic xanthoastrocytoma after gross total resection. Two years later, the tumor recurred and underwent malignant transformation to World Health Organization grade 3 pleomorphic xanthoastrocytoma. At the third resection, pathological and genomic analyses confirmed BRAF V600E mutation together with TERT promoter mutation. Following chemoradiotherapy, spinal leptomeningeal dissemination developed. After spinal irradiation, dabrafenib plus trametinib was initiated, resulting in partial radiological response and symptomatic improvement. Although regrowth occurred 10 months after initiation of targeted therapy, the patient remains alive at the time of writing. Here, we report a case of recurrent anaplastic BRAF V600E-mutant pleomorphic xanthoastrocytoma with leptomeningeal dissemination that showed a transient but clinically meaningful response to combined BRAF-MEK inhibition and spinal radiation therapy. In addition, this case raises the possibility of an association between TERT promoter mutation and leptomeningeal dissemination, although further studies are required to clarify this relationship.

BRAF-MEK抑制对TERT启动子突变间变性多形性黄色星形细胞瘤的影响:一例报告。
多形性黄色星形细胞瘤是一种罕见的脑肿瘤,常携带致癌基因BRAF V600E突变。约28.6%-47%的高级别多形性黄色星形细胞瘤与TERT启动子突变和脑膜轻散有关,目前尚无明确的治疗方法,预后仍较差。BRAF和MEK抑制剂联合治疗BRAF v600e突变脑肿瘤已被证明有效。我们报告一例22岁男性右颞叶肿瘤,经大体全切除后,最初诊断为世界卫生组织2级多形性黄色星形细胞瘤。两年后,肿瘤复发并恶性转化为世界卫生组织三级多形性黄色星形细胞瘤。第三次切除时,病理和基因组分析证实BRAF V600E突变和TERT启动子突变。放化疗后,脊髓脊髓轻脑膜播散。脊柱照射后,开始使用达非尼加曲美替尼,导致部分放射反应和症状改善。虽然在开始靶向治疗10个月后出现了再生,但在撰写本文时患者仍然存活。在这里,我们报告了一例复发性间变性BRAF v600e突变多形性黄质星形细胞瘤伴轻脑膜播散,该病例对BRAF- mek联合抑制和脊柱放射治疗表现出短暂但有临床意义的反应。此外,该病例提出了TERT启动子突变与轻脑膜传播之间存在关联的可能性,尽管需要进一步的研究来阐明这种关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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