TY - JOUR
T1 - Checkpoint inhibitor immunotherapy for glioblastoma
T2 - current progress, challenges and future outlook
AU - Gedeon, Patrick C.
AU - Champion, Cosette D.
AU - Rhodin, Kristen E.
AU - Woroniecka, Karolina
AU - Kemeny, Hanna R.
AU - Bramall, Alexa N.
AU - Bernstock, Joshua D.
AU - Choi, Bryan D.
AU - Sampson, John H.
N1 - Funding Information:
This work was supported by funding from the National Institutes of Health: F30CA196199 (P.C. Gedeon), R01NS085412 (J.H. Sampson), U01NS090284 (J.H. Sampson), R01CA177476 (J.H. Sampson), R01NS086943 (J.H. Sampson), and R01NS099463 (J.H. Sampson). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. Figures 1, 2, and 3 were illustrated specifically for this manuscript by Megan Llewellyn, MSMI. Copyright Duke University. Printed here with permission under a CC-BY 4.0 license.
Publisher Copyright:
© 2020 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2020/10
Y1 - 2020/10
N2 - Introduction: Despite maximal surgical resection and chemoradiation, glioblastoma (GBM) continues to be associated with significant morbidity and mortality. Novel therapeutic strategies are urgently needed. Given success in treating multiple other forms of cancer, checkpoint inhibitor immunotherapy remains foremost amongst novel therapeutic strategies that are currently under investigation. Areas covered: Through a systematic review of both published literature and the latest preliminary data available from ongoing clinical studies, we provide an up-to-date discussion on the immune system in the CNS, a detailed mechanistic evaluation of checkpoint biology in the CNS along with evidence for disruption of these pathways in GBM, and a summary of available preclinical and clinical data for checkpoint blockade in GBM. We also include a discussion of novel, emerging targets for checkpoint blockade which may play an important role in GBM immunotherapy. Expert opinion: Evidence indicates that while clinical success of checkpoint blockade for the treatment of GBM has been limited to date, through improved preclinical models, optimization in the context of standard of care therapies, assay standardization and harmonization, and combinatorial approaches which may include novel targets for checkpoint blockade, checkpoint inhibitor immunotherapy may yield a safe and effective therapeutic option for the treatment of GBM.
AB - Introduction: Despite maximal surgical resection and chemoradiation, glioblastoma (GBM) continues to be associated with significant morbidity and mortality. Novel therapeutic strategies are urgently needed. Given success in treating multiple other forms of cancer, checkpoint inhibitor immunotherapy remains foremost amongst novel therapeutic strategies that are currently under investigation. Areas covered: Through a systematic review of both published literature and the latest preliminary data available from ongoing clinical studies, we provide an up-to-date discussion on the immune system in the CNS, a detailed mechanistic evaluation of checkpoint biology in the CNS along with evidence for disruption of these pathways in GBM, and a summary of available preclinical and clinical data for checkpoint blockade in GBM. We also include a discussion of novel, emerging targets for checkpoint blockade which may play an important role in GBM immunotherapy. Expert opinion: Evidence indicates that while clinical success of checkpoint blockade for the treatment of GBM has been limited to date, through improved preclinical models, optimization in the context of standard of care therapies, assay standardization and harmonization, and combinatorial approaches which may include novel targets for checkpoint blockade, checkpoint inhibitor immunotherapy may yield a safe and effective therapeutic option for the treatment of GBM.
KW - antibodies
KW - Cancer
KW - checkpoint inhibitors
KW - clinical trials
KW - glioma
KW - immunotherapy
UR - http://www.scopus.com/inward/record.url?scp=85090961530&partnerID=8YFLogxK
U2 - 10.1080/17512433.2020.1817737
DO - 10.1080/17512433.2020.1817737
M3 - Review article
C2 - 32862726
AN - SCOPUS:85090961530
SN - 1751-2433
VL - 13
SP - 1147
EP - 1158
JO - Expert Review of Clinical Pharmacology
JF - Expert Review of Clinical Pharmacology
IS - 10
ER -