医学
免疫系统
嵌合抗原受体
胶质瘤
放射治疗
肿瘤微环境
中枢神经系统
T细胞
促炎细胞因子
舱室(船)
癌症研究
免疫学
炎症
内科学
海洋学
地质学
作者
Bryce C. Thomas,Dilana E. Staudt,Alicia M. Douglas,Michelle Monje,Nicholas A. Vitanza,Matthew D. Dun
标识
DOI:10.1016/j.trecan.2023.07.007
摘要
Diffuse midline glioma (DMG) is a fatal pediatric cancer of the central nervous system (CNS). The location and infiltrative nature of DMG prevents surgical resection and the benefits of palliative radiotherapy are temporary; median overall survival (OS) is 9-11 months. The tumor immune microenvironment (TIME) is 'cold', and has a dominant immunosuppressive myeloid compartment with low levels of infiltrating lymphocytes and proinflammatory molecules. Because survival statistics have been stagnant for many decades, and therapies targeting the unique biology of DMG are urgently needed, this has prompted the clinical assessment of chimeric antigen receptor (CAR) T cell therapies in this setting. We highlight the current landscape of CAR T cell therapy for DMG, the role the TIME may play in the response, and strategies to overcome treatment obstacles.
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