用曲美替尼抑制MEK是治疗神经节胶质瘤的成功方法。

Clinical case reports and reviews Pub Date : 2020-06-01 Epub Date: 2020-05-08
Eliza Baird Daniel, Douglas E Ney, Jean M Mulcahy Levy
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引用次数: 0

摘要

神经节神经胶质瘤主要是由神经元和神经胶质成分组成的低级别原发性脑肿瘤,常见于儿科和青年人群。在大多数情况下,手术切除这些肿瘤是可以治愈的。然而,肿瘤位于大脑的重要中心可能使手术干预不合适。此外,一部分肿瘤发展为间变性神经节胶质瘤,尽管切除,预后也很差。MAPK通路的激活突变,如BRAF V600E,已经在许多这些肿瘤中被发现。携带这种突变的肿瘤对MEK抑制疗法表现出易感性。然而,仍有一部分神经节胶质瘤在MAPK通路中不包含已知的突变,因此未被MEK抑制治疗靶向。在这里,我们介绍了一位年轻的成年神经节胶质瘤患者,没有确定的MAPK通路激活突变,他对曲美替尼的MEK抑制表现出显著和持续的反应。
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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MEK inhibition with trametinib is a successful therapy in ganglioglioma.

Gangliogliomas are predominantly low-grade primary brain tumors comprised of neuronal and glial components that are found in both pediatric and young adult populations. In the majority of cases, surgical resection of these tumors is curative. However, tumor location in eloquent centers of the brain can make surgical intervention inappropriate. Additionally, a subset of tumors progress to anaplastic ganglioglioma which carries a poor prognosis, despite resection. Activating mutations in the MAPK pathway, such as BRAF V600E, have been identified in many of these tumors. Tumors carrying such mutations have demonstrated susceptibility to MEK inhibition therapy. However, there remains a subset of ganglioglioma that do not contain a known mutation in the MAPK pathway and thus have not been targeted with MEK inhibition therapy. Here, we present a young adult ganglioglioma patient without identified MAPK pathway activation mutations who demonstrated a significant and sustained response to MEK inhibition with trametinib.

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