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Sager et al. Neuroimmunol Neuroinflammation 2018;5:25              Neuroimmunology
               DOI: 10.20517/2347-8659.2018.12                              and Neuroinflammation




               Review                                                                        Open Access


               A concise review of immunotherapy for glioblastoma


               Omer Sager, Ferrat Dincoglan, Selcuk Demiral, Bora Uysal, Hakan Gamsiz, Bahar Dirican,
               Murat Beyzadeoglu
               Department of Radiation Oncology, University of Health Sciences, Gulhane Medical Faculty, Ankara 06018, Turkey.

               Correspondence to:  Assoc.  Prof. Omer Sager,  Department  of  Radiation Oncology,  University of  Health  Sciences,  Gulhane
               Medical Faculty, Gn.Tevfik Sağlam Cd. Etlik , Ankara 06018, Turkey. E-mail: omersager@gmail.com

               How to cite this article: Sager O, Dincoglan F, Demiral S, Uysal B, Gamsiz H, Dirican B, Beyzadeoglu M. A concise review of
               immunotherapy for glioblastoma. Neuroimmunol Neuroinflammation 2018;5:25. http://dx.doi.org/10.20517/2347-8659.2018.12
               Received: 26 Mar 2018    First Decision: 26 Apr 2018    Revised: 31 May 2018    Accepted: 5 Jun 2018    Published: 15 Jun 2018

               Science Editor: Athanassios P. Kyritsis    Copy Editor: Jun-Yao Li    Production Editor: Cai-Hong Wang



               Abstract
               Glioblastoma (GB) is the most common and aggressive form of primary brain tumors in adults with a universally poor
               prognosis despite multimodal management including surgery, chemotherapy and radiation therapy. Among the novel
               therapeutic strategies, immunotherapy deserves particular attention with its potential to evoke biologic response and
               harness the host immune system. Considerable success achieved for other tumors has elicited great enthusiasm and
               prompted research on immunotherapy for GB. While the central nervous system has traditionally been thought of
               as an immune-privileged site, our understanding is being refined with emerging evidence. Several studies have been
               conducted and more are under way to establish the role of immunotherapy in management of GB. Immunotherapy of GB
               has yet resulted in mixed success with conflicting research findings, emphasizing the need for extensive study before its
               integration into routine clinical practice. Although there is a lot of room for improvement, immunotherapy for GB may be
               feasible and serve as a viable management strategy broadening and strengthening the therapeutic armamentarium to
               combat this deadly disease. Herein, we present a concise review of immunotherapy for GB.

               Keywords: Glioblastoma, immunotherapy, glioma, vaccine, passive immunotherapy, active immunotherapy, cytokine
               therapy, central nervous system



               INTRODUCTION
               Glioblastoma (GB) constitutes the most common and aggressive form of primary brain tumors in
               adults . Management of newly diagnosed GB includes maximal tumor resection followed by adjuvant
                    [1]
               chemoradiotherapy. The landmark study by European Organisation for Research and Treatment of Cancer
               (EORTC)/National Cancer Institute of Canada Clinical Trials Group (NCIC-CTG) in 2005 has reported

                           © The Author(s) 2018. Open Access This article is licensed under a Creative Commons Attribution 4.0
                           International License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use,
                sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long
                as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license,
                and indicate if changes were made.


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