Current State of Immunotherapy for Treatment of Glioblastoma
- PMID: 30790064
- PMCID: PMC6394457
- DOI: 10.1007/s11864-019-0619-4
Current State of Immunotherapy for Treatment of Glioblastoma
Abstract
At this time, there are no FDA-approved immune therapies for glioblastoma (GBM) despite many unique therapies currently in clinical trials. GBM is a highly immunosuppressive tumor and there are limitations to a safe immune response in the central nervous system. To date, there have been several failures of phase 3 immune therapy clinical trials in GBM. These trials have targeted single components of an antitumor immune response. Learning from these failures, the future of immunotherapy for GBM appears most hopeful for combination of immune therapies to overcome the profound immunosuppression of this disease. Understanding biomarkers for appropriate patient selection as well as tumor progression are necessary for implementation of immunotherapy for GBM.
Keywords: CAR-T; Checkpoint inhibitors; Glioblastoma; Immunotherapy; Vaccine.
Conflict of interest statement
Conflict of Interest
Tresa McGranahan declares that she has no conflict of interest. Kate Elizabeth Therkelsen declares that she has no conflict of interest. Sarah Ahmad declares that she has no conflict of interest. Seema Nagpal has received clinical trial funding from Inovio/Regeneron and Tocagen, has received research support from Nektar Therapeutics, and has received compensation from Nektar Therapeutics for service as a consultant.
Human and Animal Rights and Informed Consent
This article does not contain any studies with human or animal subjects performed by any of the authors.
Similar articles
-
Advances in Experimental Targeted Therapy and Immunotherapy for Patients with Glioblastoma Multiforme.Anticancer Res. 2017 Jan;37(1):21-33. doi: 10.21873/anticanres.11285. Anticancer Res. 2017. PMID: 28011470 Review.
-
Clinical Trials Investigating Immune Checkpoint Blockade in Glioblastoma.Curr Treat Options Oncol. 2017 Aug;18(8):51. doi: 10.1007/s11864-017-0492-y. Curr Treat Options Oncol. 2017. PMID: 28785997 Review.
-
Treatment Progress of Immune Checkpoint Blockade Therapy for Glioblastoma.Front Immunol. 2020 Nov 30;11:592612. doi: 10.3389/fimmu.2020.592612. eCollection 2020. Front Immunol. 2020. PMID: 33329578 Free PMC article. Review.
-
Immunotherapy as a New Therapeutic Approach for Brain and Spinal Cord Tumors.Adv Exp Med Biol. 2023;1394:73-84. doi: 10.1007/978-3-031-14732-6_5. Adv Exp Med Biol. 2023. PMID: 36587382
-
An Update on the Role of Immunotherapy and Vaccine Strategies for Primary Brain Tumors.Curr Treat Options Oncol. 2015 Nov;16(11):54. doi: 10.1007/s11864-015-0371-3. Curr Treat Options Oncol. 2015. PMID: 26454859 Review.
Cited by
-
IL-18, a therapeutic target for immunotherapy boosting, promotes temozolomide chemoresistance via the PI3K/AKT pathway in glioma.J Transl Med. 2024 Oct 21;22(1):951. doi: 10.1186/s12967-024-05755-x. J Transl Med. 2024. PMID: 39434175 Free PMC article.
-
Oncolytic Virotherapy in Glioma Tumors.Int J Mol Sci. 2020 Oct 14;21(20):7604. doi: 10.3390/ijms21207604. Int J Mol Sci. 2020. PMID: 33066689 Free PMC article. Review.
-
Engineered smart materials for RNA based molecular therapy to treat Glioblastoma.Bioact Mater. 2023 Nov 27;33:396-423. doi: 10.1016/j.bioactmat.2023.11.007. eCollection 2024 Mar. Bioact Mater. 2023. PMID: 38059120 Free PMC article.
-
Considering the Experimental use of Temozolomide in Glioblastoma Research.Biomedicines. 2020 Jun 4;8(6):151. doi: 10.3390/biomedicines8060151. Biomedicines. 2020. PMID: 32512726 Free PMC article. Review.
-
Preclinical Modeling of Surgery and Steroid Therapy for Glioblastoma Reveals Changes in Immunophenotype that are Associated with Tumor Growth and Outcome.Clin Cancer Res. 2021 Apr 1;27(7):2038-2049. doi: 10.1158/1078-0432.CCR-20-3262. Epub 2021 Feb 4. Clin Cancer Res. 2021. PMID: 33542075 Free PMC article.
References
References and Recommended Reading
Papers of particular interest, published recently, have been highlighted as: • Of importance •• Of major importance
-
- Chongsathidkiet P, Jackson C, Koyama S, Loebel F, Cui X, Farber SH, Woroniecka K, Elsamadicy AA, Dechant CA, Kemeny HR, Sanchez-Perez L, Cheema TA, Souders NC, Herndon JE, Coumans JV, Everitt JI, Nahed BV, Sampson JH, Gunn MD, Martuza RL, Dranoff G, Curry WT, Fecci PE. Sequestration of T cells in bone marrow in the setting of glioblastoma and other intracranial tumors. Nat Med. 2018;24:1459–1468. doi: 10.1038/s41591-018-0135-2. - DOI - PMC - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical