TY - JOUR
T1 - Advanced Immunotherapy Approaches for Glioblastoma
AU - Ma, Yifan
AU - Yang, Zhaogang
AU - Huntoon, Kristin
AU - Jiang, Wen
AU - Kim, Betty Y.S.
N1 - Funding Information:
Y.M. and Z.Y. contributed equally to this work. The authors thank Jonathan Feinberg for editing the manuscript. This work was supported by grant from the National Cancer Institute R21 5R21CA252344 (Z.Y.).
Publisher Copyright:
© 2021 Wiley-VCH GmbH
PY - 2021/8
Y1 - 2021/8
N2 - Glioblastoma multiforme (GBM) is the most aggressive primary central nervous system (CNS) tumor, and treatment for GBM is regarded as the most challenging task in clinical oncology. Although multiple treatments are available, including surgery, chemotherapy, and radiotherapy, these conventional therapies barely improve the functional prognosis and life quality of patients with glioblastoma. Immunotherapy, has become a promising approach for treating GBM because of the ability to overcome the blood–brain barrier (BBB) and complicated unique tumor immune microenvironment. Developing an efficient immunotherapy for GBM requires understanding the glioblastoma immune microenvironment; accordingly, this study begins by summarizing this and what it indicates for the development of immunological effects. Then current immunotherapy management for GBM and advanced studies including checkpoint inhibitors, cell vaccines, and extracellular vesicle-based immunotherapy is reviewed. Because monotherapies are inadequate for treating GBM, combinational GBM immunotherapy with other classical cancer therapies, especially chemo-immunotherapy, radiotherapy-immunotherapy, and the combination of gene therapy and immunotherapy, is introduced and discussed. The recent progress introduced in this review suggests that cancer immunotherapy and its combinatory therapies are highly promising treatment modalities for glioblastoma patients. However, systematical and in-depth investigations are required to improve the efficacy of GBM immunotherapy for future clinical translation.
AB - Glioblastoma multiforme (GBM) is the most aggressive primary central nervous system (CNS) tumor, and treatment for GBM is regarded as the most challenging task in clinical oncology. Although multiple treatments are available, including surgery, chemotherapy, and radiotherapy, these conventional therapies barely improve the functional prognosis and life quality of patients with glioblastoma. Immunotherapy, has become a promising approach for treating GBM because of the ability to overcome the blood–brain barrier (BBB) and complicated unique tumor immune microenvironment. Developing an efficient immunotherapy for GBM requires understanding the glioblastoma immune microenvironment; accordingly, this study begins by summarizing this and what it indicates for the development of immunological effects. Then current immunotherapy management for GBM and advanced studies including checkpoint inhibitors, cell vaccines, and extracellular vesicle-based immunotherapy is reviewed. Because monotherapies are inadequate for treating GBM, combinational GBM immunotherapy with other classical cancer therapies, especially chemo-immunotherapy, radiotherapy-immunotherapy, and the combination of gene therapy and immunotherapy, is introduced and discussed. The recent progress introduced in this review suggests that cancer immunotherapy and its combinatory therapies are highly promising treatment modalities for glioblastoma patients. However, systematical and in-depth investigations are required to improve the efficacy of GBM immunotherapy for future clinical translation.
KW - cancer immunotherapy
KW - combination therapy
KW - glioblastoma multiforme
KW - immune microenvironment
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U2 - 10.1002/adtp.202100046
DO - 10.1002/adtp.202100046
M3 - Review article
AN - SCOPUS:85108912611
SN - 2366-3987
VL - 4
JO - Advanced Therapeutics
JF - Advanced Therapeutics
IS - 8
M1 - 2100046
ER -