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Immune Checkpoint in Glioblastoma: Promising and Challenging

Overview
Journal Front Pharmacol
Date 2017 May 25
PMID 28536525
Citations 89
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Abstract

Glioblastoma (GBM) is a severe malignant brain cancer with poor overall survival. Conventional intervention remains dismal to prevent recurrence and deterioration of GBM cell. Recent years have witnessed exciting breakthroughs in novel immune strategies, especially checkpoint inhibitors, some of which have become adjuvant setting after standard of care in melanoma. Several clinical trials of checkpoint inhibitors are ongoing in glioblastoma and other brain carcinomas. Plus, synergistic combinations of checkpoint inhibitors with conventional therapy strategies-radiotherapy, temozolomide, bevacizumab, and corticosteroids are now being exploited and applied in clinical settings. This review highlights the recent developments of checkpoints in GBM immunotherapy to provide a brief and comprehensive review of current treatment options. Furthermore, we will discuss challenges remained, such as unique immune system of central nervous system (CNS), immune-related toxicities, synergies, and adverse interactions of combination therapies.

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References
1.
Deng R, Cassady K, Li X, Yao S, Zhang M, Racine J . B7H1/CD80 interaction augments PD-1-dependent T cell apoptosis and ameliorates graft-versus-host disease. J Immunol. 2014; 194(2):560-74. PMC: 4282988. DOI: 10.4049/jimmunol.1402157. View

2.
Bordon Y . Tumour immunology: A checkpoint for NK cells. Nat Rev Immunol. 2016; 16(7):402-3. DOI: 10.1038/nri.2016.68. View

3.
Zang X, Allison J . The B7 family and cancer therapy: costimulation and coinhibition. Clin Cancer Res. 2007; 13(18 Pt 1):5271-9. DOI: 10.1158/1078-0432.CCR-07-1030. View

4.
Wolchok J, Kluger H, Callahan M, Postow M, Rizvi N, Lesokhin A . Nivolumab plus ipilimumab in advanced melanoma. N Engl J Med. 2013; 369(2):122-33. PMC: 5698004. DOI: 10.1056/NEJMoa1302369. View

5.
Jiang H, Hegde S, Knolhoff B, Zhu Y, Herndon J, Meyer M . Targeting focal adhesion kinase renders pancreatic cancers responsive to checkpoint immunotherapy. Nat Med. 2016; 22(8):851-60. PMC: 4935930. DOI: 10.1038/nm.4123. View