Treatment Progress of Immune Checkpoint Blockade Therapy for Glioblastoma

被引:38
|
作者
Zhang, Na [1 ]
Wei, Li [1 ]
Ye, Meng [2 ]
Kang, Chunsheng [1 ,3 ]
You, Hua [1 ]
机构
[1] Guangzhou Med Univ, Affiliated Canc Hosp & Inst, Med Oncol Dept, Guangzhou, Peoples R China
[2] Ningbo Univ, Med Oncol Dept, Affiliated Hosp, Med Sch, Ningbo, Peoples R China
[3] Tianjin Med Univ Gen Hosp, Tianjin Neurol Inst, Key Lab Postneuroinjury Neurorepair & Regenerat C, Dept Neurosurg,Lab Neurooncol, Tianjin, Peoples R China
来源
FRONTIERS IN IMMUNOLOGY | 2020年 / 11卷
基金
中国国家自然科学基金;
关键词
glioblastoma; immunotherapy; checkpoint inhibitors; checkpoint blockade therapy; resistance mechanism; TUMOR; RESISTANCE; IMMUNOTHERAPY; INFILTRATION; NEOANTIGENS; INHIBITION; ONCOLOGY;
D O I
10.3389/fimmu.2020.592612
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Glioblastoma (GBM) is a highly malignant and aggressive primary brain tumor mostly prevalent in adults and is associated with a very poor prognosis. Moreover, only a few effective treatment regimens are available due to their rapid invasion of the brain parenchyma and resistance to conventional therapy. However, the fast development of cancer immunotherapy and the remarkable survival benefit from immunotherapy in several extracranial tumor types have recently paved the way for numerous interventional studies involving GBM patients. The recent success of checkpoint blockade therapy, targeting immunoinhibitory proteins such as programmed cell death protein-1 and/or cytotoxic T lymphocyte-associated antigen-4, has initiated a paradigm shift in clinical and preclinical investigations, and the use of immunotherapy for solid tumors, which would be a potential breakthrough in the field of drug therapy for the GBM treatment. However clinical trial showed limited benefits for GBM patients. The main reason is drug resistance. This review summarizes the clinical research progress of immune checkpoint molecules and inhibitors, introduces the current research status of immune checkpoint inhibitors in the field of GBM, analyzes the molecular resistance mechanism of checkpoint blockade therapy, proposes corresponding re-sensitive strategies, and describes a reference for the design and development of subsequent clinical studies on immunotherapy for GBM.
引用
收藏
页数:7
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