TY - JOUR
T1 - Advances in Immunotherapy for the Treatment of Adult Glioblastoma
T2 - Overcoming Chemical and Physical Barriers
AU - Lechpammer, Mirna
AU - Rao, Rohan
AU - Shah, Sanjit
AU - Mirheydari, Mona
AU - Bhattacharya, Debanjan
AU - Koehler, Abigail
AU - Toukam, Donatien Kamdem
AU - Haworth, Kevin J.
AU - Pomeranz Krummel, Daniel
AU - Sengupta, Soma
N1 - Funding Information:
S.S.G. is supported by the Harold C. Schott Endowment and the Pam and Tom Mischell Funds. K.J.H. is supported by NIH. grant R01HL148451. D.P.K. and K.J.H. are supported by the UCGNI and Brain Tumor Center Pilot Funds.
Publisher Copyright:
© 2022 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2022/4/1
Y1 - 2022/4/1
N2 - Glioblastoma, or glioblastoma multiforme (GBM, WHO Grade IV), is a highly aggressive adult glioma. Despite extensive efforts to improve treatment, the current standard-of-care (SOC) regimen, which consists of maximal resection, radiotherapy, and temozolomide (TMZ), achieves only a 12–15 month survival. The clinical improvements achieved through immunotherapy in several extracranial solid tumors, including non-small-cell lung cancer, melanoma, and non-Hodgkin lymphoma, inspired investigations to pursue various immunotherapeutic interventions in adult glioblastoma patients. Despite some encouraging reports from preclinical and early-stage clinical trials, none of the tested agents have been convincing in Phase III clinical trials. One, but not the only, factor that is accountable for the slow progress is the blood–brain barrier, which prevents most antitumor drugs from reaching the target in appreciable amounts. Herein, we review the current state of immunotherapy in glioblastoma and discuss the significant challenges that prevent advancement. We also provide thoughts on steps that may be taken to remediate these challenges, including the application of ultrasound technologies.
AB - Glioblastoma, or glioblastoma multiforme (GBM, WHO Grade IV), is a highly aggressive adult glioma. Despite extensive efforts to improve treatment, the current standard-of-care (SOC) regimen, which consists of maximal resection, radiotherapy, and temozolomide (TMZ), achieves only a 12–15 month survival. The clinical improvements achieved through immunotherapy in several extracranial solid tumors, including non-small-cell lung cancer, melanoma, and non-Hodgkin lymphoma, inspired investigations to pursue various immunotherapeutic interventions in adult glioblastoma patients. Despite some encouraging reports from preclinical and early-stage clinical trials, none of the tested agents have been convincing in Phase III clinical trials. One, but not the only, factor that is accountable for the slow progress is the blood–brain barrier, which prevents most antitumor drugs from reaching the target in appreciable amounts. Herein, we review the current state of immunotherapy in glioblastoma and discuss the significant challenges that prevent advancement. We also provide thoughts on steps that may be taken to remediate these challenges, including the application of ultrasound technologies.
KW - Brain tumors
KW - Gliomas
KW - Immune checkpoint inhibitors
KW - Immunotherapy
KW - Ultrasound
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U2 - 10.3390/cancers14071627
DO - 10.3390/cancers14071627
M3 - Review article
AN - SCOPUS:85126970402
VL - 14
JO - Cancers
JF - Cancers
SN - 2072-6694
IS - 7
M1 - 1627
ER -