Immunotherapy and radiation for high-grade glioma: a narrative review

被引:9
|
作者
Fakhoury, Kareem R. [1 ]
Ney, Douglas E. [2 ,3 ]
Ormond, D. Ryan [3 ]
Rusthoven, Chad G. [1 ]
机构
[1] Univ Colorado, Anschutz Med Ctr, Dept Radiat Oncol, Aurora, CO USA
[2] Univ Colorado, Anschutz Med Ctr, Dept Neurol, Aurora, CO USA
[3] Univ Colorado, Anschutz Med Ctr, Dept Neurosurg, Aurora, CO USA
关键词
Glioblastoma (GBM); vaccine; adoptive transfer; immune checkpoint inhibitor (ICI); radiotherapy; NEWLY-DIAGNOSED GLIOBLASTOMA; CHIMERIC ANTIGEN RECEPTOR; GROWTH-FACTOR RECEPTOR; PROGRESSION-FREE SURVIVAL; LONG-TERM SURVIVAL; DENDRITIC CELL VACCINATION; RANDOMIZED PHASE-III; FIXED TUMOR VACCINE; TRANSFERRED T-CELLS; RECURRENT GLIOBLASTOMA;
D O I
10.21037/tcr-20-1933
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Glioblastoma and other high-grade gliomas (HGGs) are the most common and deadly primary brain tumors. Due to recent advances in immunotherapy and improved clinical outcomes in other disease sites, the study of immunotherapy in HGG has increased significantly. Herein, we summarize and evaluate existing evidence and ongoing clinical trials investigating the use of immunotherapy in the treatment of HGG, including therapeutic vaccination, immune checkpoint inhibition, adoptive lymphocyte transfer, and combinatorial approaches utilizing radiation and multiple modalities of immunotherapy. Special attention is given to the mechanisms by which radiation may improve immunogenicity in HGG, why this motivates the study of radiation in combination with immunotherapy, and how to determine optimal dosing and scheduling of radiation. Though larger randomized controlled trials have not consistently shown improvements in clinical outcomes, this area of research is still in its early stages and a number of important lessons can be taken away from the studies that have been completed to date. Many studies found a subset of patients who experienced durable responses, and analysis of their immune cells and tumor cells can be used to identify biomarkers that predict therapeutic response, as well as additional glioma-specific targets that can enhance therapeutic efficacy in a challenging tumor type.
引用
收藏
页码:2537 / 2570
页数:34
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