International Pleuropulmonary Blastoma/<italic>DICER1</italic> Registry, Children's Minnesota, Minneapolis, Minnesota, USA,
Cancer and Blood Disorders, Children's Minnesota, Minneapolis, Minnesota, USA,
Pediatr Neurosurg. 2022;57(1):63-68. doi: 10.1159/000519889. Epub 2021 Nov 8.
Low-grade neuroepithelial tumors are a heterogeneous group of central nervous system tumors that are generally indolent in nature but in rare instances can progress to include leptomeningeal dissemination.
We present a case of a patient with a low-grade neuroepithelial tumor of indeterminate type with symptomatic leptomeningeal dissemination despite 3 chemotherapy regimens and radiotherapy. Somatic targetable mutation testing showed an FGFR1_TACC1 fusion. Therapy with pazopanib/topotecan was initiated, and disease stabilization was achieved. He received pazopanib/topotecan for a total of 2 years and is now >2 years from completion of treatment and continues to do well with no evidence of disease.
This case highlights the utility of targetable mutation testing in therapeutic decision-making and the novel use of systemic pazopanib/topotecan therapy for refractory low-grade neuroepithelial tumor within the context of this clinical situation and specific mutation profile.
低级别神经上皮肿瘤是一组异质性中枢神经系统肿瘤,通常性质惰性,但在极少数情况下会进展为包括软脑膜播散。
我们报告了一例低级别神经上皮肿瘤,不定型,尽管接受了 3 种化疗方案和放疗,但仍有症状性软脑膜播散。体细胞靶向突变检测显示 FGFR1_TACC1 融合。开始使用帕唑帕尼/拓扑替康治疗,疾病稳定。他总共接受了 2 年的帕唑帕尼/拓扑替康治疗,目前已完成治疗 2 年以上,且情况良好,无疾病证据。
本病例强调了靶向突变检测在治疗决策中的应用价值,以及在这种临床情况下和特定突变谱中,系统使用帕唑帕尼/拓扑替康治疗难治性低级别神经上皮肿瘤的新方法。