医学
多形性黄色星形细胞瘤
疾病
肿瘤科
靶向治疗
内科学
病理
并发症
放射治疗
免疫疗法
癌症
胶质母细胞瘤
完全响应
替莫唑胺
转移性黑色素瘤
进行性疾病
个性化医疗
贝伐单抗
星形细胞瘤
外科
易普利姆玛
精密医学
转移
诱导疗法
威罗菲尼
放射科
癌症治疗
作者
Maria Jacome,Robert Macaulay,Sheethal Cyriac,Solmaz Sahebjam,Arnold Etame,Michael Yu,Yolanda Pina
出处
期刊:Neuro-oncology
[Oxford University Press]
日期:2025-11-01
卷期号:27 (Supplement_5): v47-v47
标识
DOI:10.1093/neuonc/noaf201.0184
摘要
Abstract Leptomeningeal disease (LMD) is a rare metastatic complication with a grim prognosis for most patients and limited treatment strategies. Therapy is adjusted to the primary tumor from which it arises. Targeted therapies and personalized medicine have become cornerstones in cancer treatment but its utility in LMD has been limited. In here we report a case of a female patient who developed LMD from a Pleomorphic Xanthoastrocytoma (PXA), BRAFV600-mutated, who has shown successful response to treatment with BRAF/MEKi (Encorafinib/Binimetinib) for almost four years since initial LMD diagnosis. The effectiveness of therapy in this patient was initially observed as stable disease, with radiographic progression if BRAF/MEKi were withheld, and immediate control achieved when reinstated. Despite being just one case, this hopefully could serve as proof-of-concept for use of targeted therapy for BRAF V600E-mutated tumors with LMD progression. Patient is well up to date and to our knowledge, this is the first case reported in the literature of a PXA with LMD with successful response to targeted therapy.
科研通智能强力驱动
Strongly Powered by AbleSci AI