Prospects of immune checkpoint modulators in the treatment of glioblastoma

被引:330
作者
Preusser, Matthias [1 ,2 ]
Lim, Michael [3 ]
Hafler, David A. [4 ]
Reardon, David A. [5 ]
Sampson, John H. [6 ]
机构
[1] Med Univ Vienna, Dept Med 1, A-1090 Vienna, Austria
[2] Med Univ Vienna, Ctr Comprehens Canc, CNS Tumours Unit, A-1090 Vienna, Austria
[3] Johns Hopkins Univ, Sch Med, Baltimore, MD 21287 USA
[4] Yale Univ, Dept Neurol, Sch Med, Yale New Haven Hosp, New Haven, CT 06520 USA
[5] Dana Farber Canc Inst, Ctr Neurooncol, Boston, MA 02215 USA
[6] Duke Univ, Sch Med, Div Neurosurg, Durham, NC 27705 USA
关键词
TUMOR-INFILTRATING LYMPHOCYTES; RESPONSE ASSESSMENT CRITERIA; PRIMARY BRAIN-TUMORS; LIGAND; PD-L1; NIVOLUMAB ANTI-PD-1; ADVANCED MELANOMA; CTLA-4; BLOCKADE; CLINICAL-RESPONSE; B7-H1; EXPRESSION; PATIENTS PTS;
D O I
10.1038/nrneurol.2015.139
中图分类号
R74 [神经病学与精神病学];
学科分类号
100204 [神经病学];
摘要
Glioblastoma is the most common primary brain tumour in adults. Prognosis is poor: even with the current gold-standard first-line treatment-maximal safe resection and combination of radiotherapy with temozolomide chemotherapy-the median overall survival time is only approximately 15-17 months, because the tumour recurs in virtually all patients, and no commonly accepted standard treatment for recurrent disease exists. Several targeted agents have failed to improve patient outcomes in glioblastoma. Immunotherapy with immune checkpoint inhibitors such as ipilimumab, nivolumab, and pembrolizumab has provided relevant clinical improvements in other advanced tumours for which conventional therapies have had limited success, making immunotherapy an appealing strategy in glioblastoma. This Review summarizes current knowledge on immune checkpoint modulators and evaluates their potential role in glioblastoma on the basis of preclinical studies and emerging clinical data. Furthermore, we discuss challenges that need to be considered in the clinical development of drugs that target immune checkpoint pathways in glioblastoma, such as specific properties of the immune system in the CNS, issues with radiological response assessment, and potential interactions with established and emerging treatment strategies.
引用
收藏
页码:504 / 514
页数:11
相关论文
共 113 条
[1]
Tim-3: An Emerging Target in the Cancer Immunotherapy Landscape [J].
Anderson, Ana C. .
CANCER IMMUNOLOGY RESEARCH, 2014, 2 (05) :393-398
[2]
[Anonymous], 2014, AV BEV PRESCR INF
[3]
[Anonymous], 2014, OPD NIV PRESCR INF
[4]
[Anonymous], 2015, KEYTR PEMBR PRESCR I
[5]
PD-1 Blockade with Nivolumab in Relapsed or Refractory Hodgkin's Lymphoma [J].
Ansell, Stephen M. ;
Lesokhin, Alexander M. ;
Borrello, Ivan ;
Halwani, Ahmad ;
Scott, Emma C. ;
Gutierrez, Martin ;
Schuster, Stephen J. ;
Millenson, Michael M. ;
Cattry, Deepika ;
Freeman, Gordon J. ;
Rodig, Scott J. ;
Chapuy, Bjoern ;
Ligon, Azra H. ;
Zhu, Lili ;
Grosso, Joseph F. ;
Kim, Su Young ;
Timmerman, John M. ;
Shipp, Margaret A. ;
Armand, Philippe .
NEW ENGLAND JOURNAL OF MEDICINE, 2015, 372 (04) :311-319
[6]
Nivolumab (anti-PD-1; BMS-936558, ONO-4538) in combination with platinum-based doublet chemotherapy (PT-DC) in advanced non-small cell lung cancer (NSCLC). [J].
Antonia, Scott Joseph ;
Brahmer, Julie R. ;
Gettinger, Scott N. ;
Chow, Laura Quan Man ;
Juergens, Rosalyn A. ;
Shepherd, Frances A. ;
Laurie, Scott Andrew ;
Gerber, David E. ;
Goldman, Jonathan Wade ;
Shen, Yun ;
Harbison, Christopher ;
Alaparthy, Suresh ;
Chen, Allen C. ;
Borghaei, Hossein ;
Rizvi, Naiyer A. .
JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (15)
[7]
Nivolumab (anti-PD-1; BMS-936558, ONO-4538) and ipilimumab in first-line NSCLC: Interim phase I results. [J].
Antonia, Scott Joseph ;
Gettinger, Scott N. ;
Chow, Laura Quan Man ;
Juergens, Rosalyn A. ;
Borghaei, Hossein ;
Shen, Yun ;
Harbison, Christopher ;
Chen, Allen C. ;
Ready, Neal ;
Rizvi, Naiyer A. .
JOURNAL OF CLINICAL ONCOLOGY, 2014, 32 (15)
[8]
Distinct effects of human glioblastoma immunoregulatory molecules programmed cell death ligand-1 (PDL-1) and indoleamine 2,3-dioxygenase (IDO) on tumour-specific T cell functions [J].
Avril, Tony ;
Saikali, Stephan ;
Vauleon, Elodie ;
Jary, Anne ;
Hamlat, Abderrahmane ;
De Tayrac, Marie ;
Mosser, Jean ;
Quillien, Veronique .
JOURNAL OF NEUROIMMUNOLOGY, 2010, 225 (1-2) :22-33
[9]
The nature of activatory and tolerogenic dendritic cell-derived signal II [J].
Bakdash, Ghaith ;
Sittig, Simone P. ;
van Dijk, Tjeerd ;
Figdor, Carl G. ;
de Vries, L. Jolanda M. .
FRONTIERS IN IMMUNOLOGY, 2013, 4
[10]
Focal Radiation Therapy Combined with 4-1BB Activation and CTLA-4 Blockade Yields Long-Term Survival and a Protective Antigen-Specific Memory Response in a Murine Glioma Model [J].
Belcaid, Zineb ;
Phallen, Jillian A. ;
Zeng, Jing ;
See, Alfred P. ;
Mathios, Dimitrios ;
Gottschalk, Chelsea ;
Nicholas, Sarah ;
Kellett, Meghan ;
Ruzevick, Jacob ;
Jackson, Christopher ;
Albesiano, Emilia ;
Durham, Nicholas M. ;
Ye, Xiaobu ;
Tran, Phuoc T. ;
Tyler, Betty ;
Wong, John W. ;
Brem, Henry ;
Pardoll, Drew M. ;
Drake, Charles G. ;
Lim, Michael .
PLOS ONE, 2014, 9 (07)