Immunotherapy of glioblastoma: Recent advances and future prospects.

Glioblastoma (GBM) stands out as the most common, aggressive form of primary malignant brain tumor conferring a devastatingly poor prognosis. Despite aggressive standard-of-care in surgical resection and chemoradiation with temozolomide, the median overall survival of patients still remains no longer than 15 months, due to significant tumor heterogeneity, immunosuppression induced by the tumor immune microenvironment and low mutational burden. Advances in immunotherapeutic approaches have revolutionized the treatment of various cancer types and become conceptually attractive for glioblastoma. In this review, we provide an overview of the basic knowledge underlying immune targeting and promising immunotherapeutic strategies including CAR T cells, oncolytic viruses, cancer vaccines, and checkpoint blockade inhibitors that have been recently investigated in glioblastoma. Current clinical trials and previous clinical trial findings are discussed, shedding light on novel strategies to overcome various limitations and challenges.

Introduction

Glioblastoma (GBM) remains the most prevalent and malignant glial tumor (WHO grade IV astrocytoma), which represents more than 50% of all primary brain tumors in the United States, with an annual incidence of roughly 3 per 100,000 people.[1] Until now, it is highly aggressive and recalcitrant to almost all current standard-of-care treatments, which entail chemotherapy and radiation following complete resection. Despite such aggressive regimens, the median overall survival of patients remains no longer than 15 months from enrollment just prior to radiation therapy and concomitant chemotherapy with temozolomide, with a 5-year survival rate less than 10%.[2-4] The success of immunotherapy has been established in various solid tumors, including melanoma, prostate cancer, non-small-cell lung cancer, and renal cell carcinoma, bourgeoning success in the thriving field of immunotherapy.[5] According to recent advances in our understanding of GBM, its characteristics of rapid growth rate, proclivity to infiltrate vital brain compartments, molecular heterogeneity, regenerative capability of treatment-resistant cancer cells, and controlling concentrations of chemotherapeutic agents in the central nervous system (CNS) at lower levels have been contributing to its inexorable recurrence, resistance to therapy, and rapid progression.[6]

This review covers several major immunotherapeutic modalities targeting GBMs, including chimeric antigen receptor (CAR) T cells, oncolytic viruses (OVs), cancer vaccines, checkpoint blockade inhibitors, and combinatorial therapies (Figure 1). We will also briefly discuss the rationale of these approaches, along with its limitations and unique challenges faced when treating GBMs.

Figure 1.

Overview of the current immunotherapeutic modalities for the treatment of glioblastoma.

CNS immune privilege

The central nervous system was formerly recognized as an immune privileged site ascribed to the fully developed blood-brain barrier (BBB) and microglial surveillance. The BBB is a network of tissue and blood vessels that consists of non-fenestrated cells, forming endothelial tight junctions.[7] These semipermeable connections selectively prevent leakage of hydrophilic solutes whereas allowing the exchange of hydrophobic solutes and active transport of circulating nutrients.[8] The BBB also prevents or limits most pathogen invasion, excluding certain bacterial pathogens (Streptococcus pneumoniae, Neisseria meningitidis, group B Streptococcus, Escherichia coli) that adopted specific strategies. The strategies involve not only the release of various substances that bind to cellular receptors, resulting in the necrosis of endothelial cells or disruption of the intercellular junction, but also interactions enabling bacterial transcytosis across the endothelium.[9] Given this property, most immune cells such as lymphocytes, monocytes, and dendritic cells are blocked from entry in the quiescent state. Microglia acts as the primary immune cells of the CNS that moves constantly to survey the surrounding parenchyma, presenting antigens to lymphocytes and expressing major histocompatibility complex class II molecules (MHCII).[10] Although they can polarize to either a classical proinflammatory phenotype or to an anti-inflammatory phenotype, the immune surveillance of antigens prefers an environment that maintains neuronal homeostasis in the setting of uninflamed CNS.

It is now clear that during an CNS infection, the immune system mounts a full-scale systemic response to antigens.[11] Other events including traumatic brain injury, autoimmunity, toxicity of metabolites, or accumulation of misfolded proteins can also induce CNS inflammation, potentiating the ingress of peripheral immune cells across the BBB.[12] In 2015, structures similar to conventional lymphatic pathways paralleling the dural venous sinuses were identified in rodents, which changed our understanding of the brain’s immune environment.[13] When endogenous danger molecules are released and detected, peripheral immune cells promptly infiltrate the CNS by crossing the BBB, evoking robust inflammatory responses. It is believed that this process provides the essential substrate for immunotherapy directed toward brain tumors.[14]

Immunosuppressive mechanisms of GBM

GBM is regarded as the most aggressive form of primary brain tumor, attributing to its rapid growth rate, brain tissue infiltrating capacity, molecular heterogeneity, treatment-resistant cancer cells, and the ability to limit the concentration of chemotherapeutic agents in the CNS. Despite immunotherapy being a promising strategy, tapping into the immunological mechanism of the CNS to develop durable antitumor responses remains challenging. In fact, GBM displays similar traits that immunotherapy-responsive tumors display; however, it wields extensive immunosuppressive mechanisms and further benefits from its location in the CNS.[15] Overcoming intrinsic resistance, correcting systemic immunosuppression, countering adaptive resistance, and adjusting to acquired resistance are key for reversing the immunosuppressive machinery of GBM.[6] Intrinsic resistance reflects the molecular and clinical characteristics, including the location, tissue of origin, and its biological features. A study developed a surgical multisampling scheme that collected spatially distinct tumor fragments from 11 GBM patients, and uncovered extensive intratumor heterogeneity showing different subtypes within the same tumor.[16] This brings up a problem as selective eradication of clones susceptible to treatment is followed by progressive accelerating proliferation of resistant ones. Nevertheless, mounting an immune response that targets several diverse antigens is exceedingly risky of antigenic overlap with normal tissue for a cocktail of tumor-associated antigens (TAAs). However, it is not an issue for multiple neoantigens derived from autologous tumor cells. The ‘Three Es Hypothesis’ is an immune editing concept for understanding these interactions.[17] It describes immune cells and tumor cells engaging on a continuum of elimination, equilibrium, and escape. The immune surveillance acts as an extrinsic tumor suppressor, eliminating precancerous clones, and sculpting the phenotype of tumors by selecting the least immunogenic ones. This selective pressure leads to equilibrium and escape in the end, causing GBM to evolve and gain adaptive resistance. One study interfered with PD-1 signaling, which broadened T cells’ antitumor responses and provided more target choices via epitope spreading, allowing T cells to adapt to a tumor’s evolving molecular profile.[18] Therefore, immunotherapy should target neoantigens that is essential for tumor survival across various subtypes while being absent on healthy tissue. While neoantigens are addressed by intralesional cytolytic virus, autologous tumor antigen-based vaccines, as well as immune checkpoint inhibitors, they are not a strategy for CAR T cells or peptide vaccines.

The GBM microenvironment also plays a fundamental role in tumor immune evasion, leading to immunosuppression (Figure 2). In the uninflamed CNS, tissue-resident microglia, which functions as the main APC, make up the majority of the myeloid composition. Microglia are believed to enhance tumor infiltration in preclinical studies, leading to tumor progression and increased invasiveness. A study of cultured murine brain slices found that microglia increased the activity of metalloprotease-2, which caused increased breakdown of extracellular matrix and thereby promoted tumor invasiveness.[19] Another study showed that elevated inflammatory cytokines secreted by microglia contribute to the expansion of GBM.[20] As mentioned, the BBB guards the entry of most immune cells in the quiescent state. However, chemo-attractants secreted by the GBM cells, including CCL2, CCL5, CXCL and SDF-1 actively recruit tumor-associated macrophages (TAMs) and myeloid-derived suppressor cells (MDSCs) across the BBB.[21] Generally, TAMs have been shown to boost the expression of immune checkpoints, support cancer stem cells, and drive epithelial to mesenchymal transition (EMT), while MDSCs being the main source of TGF-β and PD-L1. Together they account for up to half of the immune compartment, significantly modulating the GBM microenvironment.[22-24] Inhibiting CCL2, CCL5 activity has been shown to reduce tumor migration and invasion.[25,26] The CCL2 secreted by GBM can induce high influx of regulatory T cells (Tregs), shifting tumor cytokine milieu toward immunosuppression, ultimately preventing the elimination of tumor cells.[27,28] GBM cells can also overexpress colony stimulating factor (CSF-1), which acts as chemo-attractants, promoting formation of high-grade gliomas in mice.[29] CSF-1 receptor inhibitors were given to patients with recurrent GBM in a phase II study, but showed no efficacy,[30] indicating that the resistance is GBM microenvironment driven.[31] Most of the newly recruited TAMs are polarized into anti-inflammatory M2 macrophages via the direct influence of GBM cells to produce a pro-tumor microenvironment (TME). The M2 phenotype TAMs can release anti-inflammatory cytokines such as IL-6, IL-10, and TGF-β, contributing to the immunosuppressive microenvironment.[32] Furthermore, GBM cells can express complement regulators including Factor H, C1-inactivator, and CD59 to avoid complement attack, enhancing immunosuppression.[33,34]

Figure 2.

Overview of immunosuppressive pathways in glioblastoma.

Immunotherapy is currently being increasingly pursued due to its potential to address the challenges noted above. Developing a curative immunotherapy for GBM must not only overcome immunotolerance and generate sufficient responses to tumor antigens, but also circumvent the evolving escape mechanisms in the immunosuppressive microenvironment. Despite preclinical data supporting immunotherapy as a viable approach for GBM patients and arduous efforts to treat them, the results have not been translated to patients.[35] At present, ongoing studies using combinatory approaches while augmenting current immunotherapeutic strategies are pointing the way for this revolutionary treatment in cancer care.

Immunotherapeutic strategies

Chimeric antigen receptor (CAR) T cells

CAR T cells demonstrate a promising strategy to counter challenges imposed by the BBB and TME as a form of adoptive cell T cell therapy (ACT). ACT is the reinfusion of autologous or allogenic antitumor T cells to attack tumor-specific antigens that are highly expressed on the surface of tumor cells while absent on normal cells. T-cells engineered in vitro with a lentiviral vector allows the construction of an autologous cell product to stably express a high-affinity single-chain fragment variable (scFv) that is specific for a target of interest. The scFv is fused to a transmembrane region, one or more co-stimulatory domains, and an intracellular signaling domain derived from the CD3ζ molecule of the endogenous T cell receptor (TCR). This grants the autologous T cells the ability to be activated upon scFv recognition of antigen, which then induces clustering and immobilization of the CAR molecules. Signals are initiated through the tyrosine kinase ζ-associated protein of 70 kDa (ZAP70) when the ITAM domains on the CD3ζ chain are phosphorylated, thereby evoking T cell effector response that includes releasing of cytokines, proliferation, cytotoxicity, and metabolic transformations.[36] The antitumoral function of CAR T cells is thought to be mainly through release of cytokines, the granzyme and perforin axis, as well as the Fas and Fas ligand axis.[37] These attributes endow CAR T cells with the ability to overcome the immunosuppression present in the TME. Until now, CAR T cells have demonstrated great clinical efficacy against hematopoietic malignancies, but applicability of CAR T cells for GBM is still being explored (Table 1).[38]

Table 1.

Summary of CAR T cells and oncolytic viruses used in clinical trials.

Trial name (ClinicalTrials.gov Identifier)	Treatment	Phase of trial	Number of participants	Primary end point or outcomes	Summary of results
CAR T-cell therapies
NCT00730613	IL13 Rα2-targeted CAR T cells	I	3	Feasibility and safety	Grade 3 adverse events were observed, median OS 11 months
NCT02208362	IL13 Rα2-targeted CAR T cells	I	92	AEs and DLT	Ongoing study, estimated completion date 1/2022
NCT04661384	IL13 Rα2-targeted CAR T cells	I	30	AEs and OS	Ongoing study, estimated completion date 12/2023
NCT04003649	IL13 Rα2-targeted CAR T cells with or without nivolumab and ipilimumab	I	60	AEs, DLT, feasibility, and OS	Ongoing study, estimated completion date 12/2022
NCT03726515	EGFRvIII-directed CAR T cells in combination with pembrolizumab	I	7	OS, PFS, and ORR	Study completed, no available info
NCT02209376	EGFRvIII-directed CAR T cells	I	11	AEs	No DLT was observed, median OS 8 months
NCT01454596	EGFRvIII-directed CAR T cells with cyclophosphamide, fludarabine and aldesleukin	I/II	18	AEs and PFS	DLT was observed at highest dose, median OS 6.9 months
NCT04385173	B7-H3-targeted CAR T cells with temozolomide	I	12	AEs, MTD, OS, and PFS	Ongoing study, estimated completion date 6/2024
NCT04077866	B7-H3-targeted CAR T cells with or without temozolomide	I/II	40	OS and PFS	Ongoing study, estimated completion date 5/2023
NCT01109095	HER2 CMV-specific CAR T cells	I	16	DLT	Study completed, no available info
Oncolytic viral therapies
NCT02798406	DNX-2401 (Delta-24-RGD adenovirus) and i.v. pembrolizumab (anti-PD-1 antibody)	II	48	ORR by interval tumor size change	Ongoing study, expected completion 08/2023
NCT01956734)	DNX-2401 (Delta-24-RGD adenovirus) and TMZ	I	31	Number of patients with AEs	No AEs related to DNX-2401
NCT00805376	DNX-2401 (conditionally replication-competent adenovirus) ± surgery	I	37	MTD	Treatment induced tumor infiltration by CD8+ and T-bet+ cells
NCT02062827	M032 (modified strain of HSV-1) by intratumoural infusion	I	36	MTD
NCT00390299	MV-CEA (measles virus expressing carcinoembryonic antigen) before or after surgery	I	40	Toxicity and MTD	Study suspended for unknown reason
NCT02026271	Ad-RTS-hIL-12 (INXN-2001, adenovirus modified to deliver hIL-2) and oral veledimex (INXN-1001, activator ligand)	I	48	Safety and tolerability	Response correlated with CD8+ (cytotoxic) and FoxP3+ (regulatory) T-cell counts in the peripheral blood
NCT02457845	G207 (modified oncolytic strain of HSV-1) single-dose inoculation	I	18	Safety and tolerability
NCT02986178	PVSRIPO (genetically recombinant nonpathogenic poliovirus:rhinovirus chimera) ± lomustine	II	62	OS at 24 months
NCT03152318	rQNestin34.5v.2 (oncolytic HSV-1) + cyclophosphamide	I	108	MTD	Ongoing study, estimated completion 07/2022
NCT03714334	DNX-2440 conditionally replication-competent adenovirus with O×40 ligand (T-cell stimulator)	I	24	Treatment-related adverse events
NCT01470794	Toca 511 (vocimagene amiretrorepvec) injection to resection cavity of recurrent glioblastoma, and Toca FC (extended-release 5-FU)	I	58	DLT	Durable complete responses were observed
NCT03330197	Ad-RTS-hIL-12 + veledimex	I	25	Safety and tolerability
NCT03896568	Ad5-DNX-2401 (oncolytic adenovirus) in bone marrow human mesenchymal stem cells	I	36	MTD	Ongoing study, estimated completion 05/2022
NCT03294486	TG6002 (modified vaccinia virus) and 5-FC	II	78	Safety, DLT, and rate of tumor progression at 6 months
NCT01301430	H-1 parvovirus (H-1PV)	II	18	Safety and DLT	No DLTs; 1 patient had a SUSAR that was not considered a DLT
NCT1491893	PVSRIPO (genetically recombinant nonpathogenic poliovirus:rhinovirus chimera)	I	61	MTD	21% long-term survivors at 36 months
NCT02197169	DNX-2401 (Delta-24-RGD adenovirus) ± IFN-γ	I	37	ORR by interval tumor size change	No benefit with the addition of IFN/IFN poorly tolerated
NCT02414165	Toca 511 (vocimagene amiretrorepvec) and Toca FC (extended release 5-FC)	II/III	403	OS	Stopped prematurely for lack of efficacy

IL13 Rα2-Specific CAR T cells

The interleukin-13 receptor subunit alpha-2 (IL13 Rα2) is a monomeric receptor for interleukin 13 that is present in up to 60% of GBMs and is associated with the activation of proinflammatory and immune pathways.[39,40] Its over-expression in GBM patients activates the phosphatidylinositol-3 kinase/AKT/mammalian target of rapamycin pathway, leading to poor prognosis and increased tumor invasiveness.[41,42] In a preclinical study, a second-generation IL13 Rα2-directed CAR T cell comprising a mutated IL13-zetakine extracellular domain (IL13.E13K.R109K) that is linked to a CD28 costimulatory and CD3ζ signaling domain was engineered. By demonstrating reduced but persisting activity against normal tissue, whereas being potently activated in the presence of IL13 Rα2, these CAR T cells proved enhanced selectivity for IL13 Rα2 over IL13Ra1/IL4Ra. Further tests applying single intracranial injections of IL13-zetakine CAR T cells in a human glioma xenograft model resulted in noticeable increases in median overall survival.[43] In 2015, a first-in-human pilot safety and feasibility trial evaluating IL13-zetakine CAR T cells was conducted in three patients with recurrent GBM. IL13 Rα2-directed CAR T cells were delivered via an implanted reservoir/catheter system into the resection cavity, inducing controllable temporary brain inflammation. Although the CAR T cells were well tolerated, adverse events were observed, including grade 3 headaches and a transient grade 3 neurologic event. Tumor tissue analysis revealed overall reduction in IL13 Rα2 expression and MRI analysis indicated a persistent increase in tumor necrotic volume, possibly extending duration of overall survival.[44] Following this trial, the group developed a second-generation IL13-zetakine CAR T cell with a 4-1BB costimulatory domain and a mutated IgG4-Fc linker to reduce off-target interactions while boosting antitumor potential. A 50-year-old man presented with recurrent GBM and multifocal leptomeningeal disease was enrolled. He was treated with 6 cycles of intracavitary infusions of CAR T cells that were administered into the resected tumor cavity followed by another 10 cycles of infusions into the ventricular system. Despite inhibiting the tumor progression locally during the intracavitary infusions, other intracranial tumors progressed and new spinal lesions were found. Subsequently, the fifth intraventricular infusion resulted in substantial reduction of all intracranial and spinal tumors with a 77–100% decrease in tumor size. However, regression of all tumors lasted for only 7.5 months and recurrence was observed at new locations along with low IL13 Rα2 expression, encouraging combinatory therapies to address the antigen-loss relapse.[45]

EGFRvIII-Specific CAR T cells

The epidermal growth factor receptor variant III (EGFRvIII), resulting from an in-frame deletion of exons 2–7 of EGFR gene, is the most common mutation of this receptor that occurs heterogeneously in up to 30% of GBM specimens.[46,47] EGFRvIII alteration was thought to be associated with shorter survival in GBM until recently suggested otherwise. Data showed that the prognosis for EGFRvIII patients might not differ from that of EGFR-amplified patients.[48] One group discovered that EGFRvIII-directed CAR T cells were able to regulate tumor growth in xenogeneic subcutaneous and orthotopic models of human EGFRvIII (+) GBM, leading to a phase I clinical trial involving patients with either residual or recurrent GBM.[49] This study was eventually terminated prior to completion as the sponsor decided to pursue combination therapies. A first-in-human study was carried out by treating a single dose of autologous EGFRvIII-directed CAR T cells to 10 patients with recurrent GBM. The results suggested that the infusion was safe and feasible, showing no off-tumor toxicities or cytokine release syndrome and noticeable levels of EGFRvIII-directed CAR T cells in the peripheral blood. Although the study was not designed for efficacy evaluation, tumor regression was not observed in any patients according to magnetic resonance imaging. In total, 7 out of 10 patients underwent surgical intervention following CAR T cell therapy and tumor tissue analysis revealed decreased EGFRvIII expression among five of them. Further investigation of the TME found increased expression of regulatory T cells as well as immunosuppressive molecules, particularly IDO1 and FoxP3, indicating immunoediting.[50] Another phase I clinical trial treated 18 patients with recurrent GBM, where the presence of EGFRvIII was confirmed by PCR and biopsy. Third-generation EGFRvIII-directed CAR T cells containing CD28 and 4-1BB costimulatory domains were delivered in a dose-escalating manner. Patients started to develop respiratory symptoms within hours post-infusion at the highest dose levels, implying that dose-limiting toxicity was reached despite showing no signs of clinical benefit. Although median overall survival was 6.9 months, 2 patients survived over a year and a third patient managed to remain alive up to 59 months post-infusion.[51] In 2019, an approach was developed to treat EGFRvIII-negative, EGFR-positive glioblastoma by combining a EGFRvIII scFv with a bispecific T-cell engager (BiTE). The BiTEs are bispecific synthetic antibodies that bind to two appropriate target antigens, serving as bridges to enhance the immune interactions and to improve antibody specificity.[52] Recently, dual receptor circuits were used in a study to integrate recognition of multiple antigens,[53] which enables controlled tumor cell death by targeting antigens that are not totally tumor specific. These SynNotch-CAR T cells improved the specificity, completeness, and persistence over conventional T cell therapy against glioblastoma.

B7-H3-Specific CAR T cells

The B7-H3 (also known as CD276), a type I transmembrane protein, plays a key role in the activation or inhibition of T-cell function. It was recognized as an important costimulatory molecule belonging to the B7 and CD28 families.[54] Until now, challenges still remain such as creation of a unified view on the receptor of the B7-H3 and further elucidation of its regulation of immune responses. Particularly, B7-H3 was found to be highly overexpressed among a wide range of human cancer cells and correlates with negative clinical outcomes as well as poor prognoses in patients, making it a valuable target for immunotherapy.[55-57] In our previous study, we constructed a third-generation B7-H3-directed CAR with 4-1BB and CD28 costimulatory domain and transduced it into T cells by lentivirus. In vitro and in vivo assessment of GBM samples from patients and cell lines was performed to analyze the antitumor effects of the engineered CAR T cells. Our results showed 58% B7-H3 positivity among the clinical samples, primary tumor cells and cell lines. B7-H3 expression level was also found to be correlated to the malignancy grade of glioma and the poor survival. In the preclinical models, potent antitumor effects of B7-H3-directed CAR T cells against GBM were demonstrated, leading to a clinical evaluation of the therapeutic potential in treating recurrent GBM at our institution.[58] A 56-year-old woman presenting with recurrent GBM in the left frontal and parietal lobe was enrolled. The patient received craniotomy and standard-of-care in the past two years. Pathological analysis revealed a high but heterogeneous B7-H3 expression, which was also confirmed by flow cytometry assay of primary tumor cells. The patient underwent intracavitary infusions of B7-H3 targeted CAR T cells in a in a dose-escalating manner for 7 cycles, after which the patient dropped out of the clinical study. Although no adverse events of grade 3 or higher were observed, the patient suffered from headaches and appeared in altered consciousness as well as drowsiness. Significant reduction of the recurrent GBM was shown by MRI analysis and clinical response sustained for up to 50 days post-infusion. Unfortunately, the tumor became resistant to the therapy and relapsed, suggesting the development of multi-antigen directed CAR T cells or using combinatory therapies.[59,60]

HER2-Specific CAR T cells

The human epidermal growth factor 2 (HER2), formerly discovered as an overexpressed TAA in certain types of breast cancer, is a transmembrane glycoprotein with an extracellular ligand binding domain and an intracellular tyrosine kinase domain.[61] HER2 is expressed across a wide array of biologically diverse CNS tumors including GBM, ependymoma, and medulloblastoma, but it is not expressed on normal CNS tissue, making it an appealing target.[62] Monoclonal antibodies, such as trastuzumab, have limited effects in CNS tumors due to the BBB and lower HER2 expression relative to breast cancer.[63] A preclinical study of HER2-specific T cells from 10 GBM patients that were generated by transduction with a retroviral vector showed promising results.[61] The group then conducted a clinical trial to treat 17 patients with progressive HER2-positive glioblastoma. They utilized a second-generation CAR encoding FRP5 (anti-Her2) scFv and a CD28 signaling endodomain. The treatments were well tolerated with CAR T cells being detected up to 12 months since the infusion while showing no dose-limiting toxic effects. However, lack of expansion of the CAR T cells and no significant survival benefit were observed with a median overall survival of 11.1 months.[64] An interim analysis of HER2-specific CAR T cells treatment for 3 young participants suggested that repeated locoregional infusion were viable and that correlative cerebrospinal fluid markers could be helpful for measuring CAR T cell activity in the CNS.[65] A recent preclinical study addresses targeting 3 antigens using a single CAR T cell product, including HER2, IL13 Rα2 and ephrin-A2 in 15 primary samples. This highlighted the improved cytokine release and cytotoxicity in comparison to monospecific or bispecific CAR T cells, shedding light on the potential utility of trivalent CAR T cell therapy for GBM.[66]

Oncolytic viruses

In recent years, OVs are a novel class of therapeutic remedy in various solid tumors treatment including GBM. OVs offer a dual mechanism of antitumor responses of tumor-specific cell killing and the induction of systemic antitumor immunity (innate and adaptive).[67] OVs induce immunogenic cell death of tumor cells. In this process, TAAs, damage-associated molecular patterns (DAMPs), and pathogen-associated molecular patterns (PAMPs) are released from the disrupted tumor cells.[68] Both DAMPs and PAMPs act as a potent stimulus for the effective innate immunity through activating the pattern recognition receptors, such as toll-like receptors. In addition, DAMPs and PAMPs can further improve the antigen cross-presentation and adaptive immune responses.[69,70] Moreover, OVs activate a proinflammatory immune response and increase the production of CXCL9, CXCL10 and CXCL11, which can promote T cells trafficking and tumor infiltration.[71]

The efficacy of OVs such as adenovirus, herpes simplex virus, measles virus, parvovirus, poliovirus, and zika virus against GBM has been demonstrated in preclinical studies.[72-76] In the case of clinical trials, a variety of OVs are currently under investigation in clinical trials with some encouraging data.[77] Initial clinical trials of OVs have showed satisfying safety profile and promising efficacy, which also offer some evidence of intratumoral viral replication and lymphocytes infiltration.[78-80] Here, we summarize ongoing clinical trials based on virotherapy for the treatment of GBM.

A phase I clinical trial (NCT01470794) showed the safety and efficacy of Toca 511 treating 56 recurrent high-grade gliomas patients. In 23 patients who are eligible for the follow-up phase III study, the median OS was 14.4 months and OS was 65.2% and 34.8% at 1 and 2 years, respectively. More encouragingly, 5 patients had a complete response and survived 33.9–52.2 months after Toca 511 treatment.[81] DNX-2401 (Delta-24-RGD; tasadenoturev) is a tumor-selective, replication-competent oncolytic adenovirus. Preclinical studies demonstrated antiglioma efficacy.[82] A phase I, dose-escalation clinical trial of DNX-2401 was tested in 37 patients with recurrent malignant glioma. The safety and response were evaluated across 8 dose levels (1 × 10e7-3 × 10e10 vp in 1 mL) in GBM patients who received a single intratumoral injection of DNX-2401. 20% of patients survived over 3 years after treatment and three patients had over 95% reduction of the enhancing tumor with a PFS of over 3 years. In another subgroup, analyses of post-treatment tumor specimens showed that DNX-2401 replicates and spreads within the tumor. In addition, DNX-2401 can induce intratumoral CD8+ and T-bet+ T cells infiltration and decrease the expression of transmembrane immunoglobulin mucin-3.[83] In Toca 511 and DNX-2401 trials, both offered encouraging results that approximately 20% of GBM patients show complete response after receiving OVs intratumorally. Meanwhile, virotherapy-associated severe adverse events are rare with no dose-limiting toxicities.[81,83]

Oncolytic H-1 parvovirus, an attenuated parvovirus, showed a slight improvement in the median OS in GBM patients who received intratumorally administration. Encouragingly, an increasing number of infiltrating lymphocytes and IFN-r levels was observed.[84]

PVSRIPO, a live attenuated poliovirus type 1 (Sabin) vaccine with its cognate internal ribosome entry site replaced with that of human rhinovirus type 2. PVSRIPO received breakthrough therapy designation from the FDA in May 2016 based on the findings of a phase I study in patients with recurrent GBM.[85] PVSRIPO recognizes the poliovirus receptor CD155, which is widely upregulated on malignant cells of solid tumors and in major components of the TME such as antigen-presenting cells.[86-88] In a phase I dose-finding and toxicity study in 61 recurrent supratentorial grade IV malignant glioma patients, convection-enhanced and intratumoral delivery of PVSRIPO was evaluated. In total, 19% of the patients had grade 3 or higher PVSRIPO-related adverse events and no neuropathogenicity or virus shedding was observed. Overall survival among the patients who received PVSRIPO reached a plateau of 21% (95% confidence interval, 11 to 33) at 24 months that was sustained at 36 months. Moreover, encouragingly, about 20% of patients remained alive for 57–70 months after the PVSRIPO injection.[89] A phase II randomized trial of PVSRIPO alone or in combination with a single cycle of lomustine in patients with recurrent grade IV malignant glioma (NCT02986178) is ongoing.

Herpes simplex virus-1 (HSV-1) is a double-stranded, linear DNA virus. HSV-1 has been widely investigated and applied to the treatment of various solid tumor including GBM.[90] HSV-1 has a large genome size of 152kb and most segments are non-essential. Therefore, HSV-1 can incorporate multiple large transgenes into its genome.[91] G207 is one genetically engineered HSV-1 variants, which contains deletion of the diploid γ1 34.5 neurovirulence gene and has viral ribonucleotide reductase (UL39) disabled by insertion of Escherichia coli lacZ.[92] A phase I clinical trial using G207 alone and with radiation to treat children and adolescents with recurrent or progressive high-grade gliomas showed no dose-limiting toxicity or serious adverse events. G207 converted immunologically “cold” tumors to “hot”.[93]

G47 delta (DELYTACT) is another oncolytic HSV-1 variant that introduces another deletion mutation based on G207. Therefore, G47 delta has triple mutation within the HSV-1 genome that can selectively kill tumor stem cells derived from GBM.[94,95] Recently, a single-arm phase II open-label, non-randomized clinical trial in Japan was completed to evaluate the safety and efficacy of G47 delta (DELYTACT) administered in adult patients with residual or recurrent GBM. Side effects were very limited with only fever observed in 2 out of 16 patients. It is noteworthy that the survival rate of 13 patients after 1 year has reached 92.3% compared with 15% for conventional drugs.[96] Based on the results of this phase II clinical trial, G47 delta (Delytact/Teserpaturev) has received conditional and time-approval from Japan Ministry of Health, Labor and Welfare (MHLW) as an OV for the treatment of patients with malignant glioma in Japan.

Some other clinical trials using OV as a treatment agent in patients with recurrent high-grade glioma are ongoing. Although promising, more clinical trials are needed to prove the safety and efficacy of the OV as a therapy for GBM.

Vaccines

Vaccine is another treatment agent against tumor that consists of tumor antigens. Vaccination can induce active immune surveillance against GBM and strengthen the adaptive immune system. Currently, there are four main approaches based on vaccine in GBM, including peptide vaccines, DNA vaccines, cell vaccines, and mRNA vaccines. Peptide or DNA vaccines involves the injection of tumor-specific antigens or DNA to induce the adaptative immune response. Cell vaccines also refer to DC vaccines based on DC cells that are derived from peripheral blood mononuclear cells (PBMCs) and are primed with tumor antigens. mRNA vaccines are some viral vectors loaded with mRNA coding tumor antigens to elicit potent immune responses. This approach has been developed over the years and are still being studied. (Table 2) However, only 3 vaccination agents have reached phase III clinical trial: Rindopepimut, DCvax, and PPV.[97-99]

Table 2.

Summary of vaccines used in clinical trials.

Trial name (ClinicalTrials.gov Identifier)	Treatment	Phase of trial	Number of participants	Primary end point or outcomes	Summary of results
NCT00458601	EGFRvIII peptide vaccine + TMZ	II	82	PFS	Median overall survival of 21.8 months and 36-month survival of 26%. Anti-EGFRvIII antibodies increased ≥4-fold in 85% of patients with duration of treatment
NCT01480479	EGFRvIII peptide vaccine + TMZ	III	745	OS	Strong humoral responses; however, no survival advantage and loss of EGFRvIII expression upon recurrence
NCT00643097	EGFRvIII peptide vaccine + DI-TMZ	II	40	PFS and hypersensitivity to peptide on the basis of a positive skin test of ≥5mm in diameter	EGFRvIII-expressing cells eradicated and vaccine immunogenic, with DI-TMZ cohort having enhanced humoral response. Median overall survival of 23.6 months
NCT00639639	CMV pp65 DC vaccine + DI-TMZ	I	16	Safety and Feasibility	Antigen-specific immune responses and median overall survival of 41.1 months in DI-TMZ cohort. A total of 36% survival 5 years from diagnosis, with four patients remaining progression-free at 59–64 months from diagnosis
NCT00045968	DCVax-L vaccine	III	348	PFS	Median overall survival of 23.1 months, with large group (n = 100) reaching 40.5 months
NCT02366728	CMV pp65 DC vaccine +111In-labeled DC vaccine + Td Toxoid + basiliximab	II	100	OS	Ongoing, have reported increased DC migration to lymph nodes following Td toxoid pre-conditioning
NCT00905060	HSPPC-96 vaccine + TMZ	II	46	Safety profile and survival durations	Median overall survival of 23.8 months. Patients with low PD-L1 expression in myeloid cells had median overall survival of 44.7 months compared to 18 months for those with high expression
NCT01280552	ICT-107 (autologous DC vaccine pulsed with synthetic peptides mimicking GAAs)	II	124	OS	Pts in the HLA-A2 subgroup showed increased ICT-107 activity immunologically with a tendency for improved clinical outcome
NCT00293423	HSPPC-96 peptide vaccine	II	41	Safety, toxicity, and PFS	Specific immune response in 11 of the 12 patients, responders had median overall survival of 11.8 months
NCT02122822	HSPPC-96 peptide vaccine + TMZ + radiotherapy	I	20	Immune response and cardiac effects	Median overall survival of 31.4 months. Patients with high tumor-specific immune responses had median overall survival of >40.5 months compared to 14.6 months for low responders
NCT02454634	IDH1 peptide vaccine	I	39	Safety and immunogenicity	A total of 93% vaccine-specific response rate, 84% survival >3 years
NCT01498328	EGFRvIII peptide vaccine + bevacizumab	II	127	PFS	24-month survival of 20% compared to 3% for controls
NCT03018288	pembrolizumab ± HSPPC-96 vaccine	II	108	1-year OS	Ongoing study, estimated completion 01/2025
NCT02149225	APVAC1 and APVAC2 (personalized peptide vaccine) plus poly-ICLC and GM-CSF	I	16	Safety and immunogenicity	Able to generate a strong and lasting immune response
NCT02924038	IMA-950 (peptide vaccine comprising multiple GAAs) and poly-ICLC ± varlilumab (immunostimulatory antiCD27 antibody)	I	30	Safety and T cell responses	Ongoing study, estimated completion 12/2022
NCT02287428	Personalized neoantigen vaccine	I	16	Safety and feasibility	Neoantigen selection is feasible and induces immune response
NCT02960230	H3.3K27 M peptide vaccine plus Td and poly-ICLC	I	29	Safety and OS	Ongoing study, estimated completion 01/2023
NCT03400917	AV-GBM-1 (Autologous dendritic cells loaded with tumor associated antigens from a short-term cell culture of autologous tumor cells)	II	55	OS	Ongoing study, estimated completion 02/2023
NCT02507583	IGF-1 R/AS ODN	I	33	Safety and tolerability	Well tolerated with an improved PFS compared with standard-of-care
NCT02455557	Montanide ISA 51 VG peptide vaccine + temozolomide	II	66	PFS	Improved PFS and OS
NCT04116658	EO2401 peptide vaccine	II	52	Safety and tolerability	Ongoing study, estimated completion 8/2023
NCT02465268	pp65-shLAMP DC dendritic cell vaccine with GM-CSF	II	175	OS	Ongoing study, estimated completion 6/2024
NCT00846456	Tumor stem cell derived mRNA- transfected dendritic cells	I/II	20	Adverse events	Progression-free survival (PFS) was 2.9 times longer in vaccinated patients
NCT01006044	Tumor lysate-pulsed autologous dendritic cell vaccine	II	26	PFS	Feasible and safe
Not Available	Personalized peptide vaccination for human leukocyte antigen (HLA)-A24+	III	88	OS	Met neither the primary nor secondary endpoints

Rindopepimut (also known as CDX-110 or PEPvIII) is a peptide-based vaccine that targets the EGFR deletion mutation in variant III of the epidermal growth factor receptor (EGFRvIII), which is expressed exclusively in GBM.[100] Targeting the EGFRvIII neoantigen that is not expressed on normal cells limits the risk of “on-target, off-tumor” toxicities. However, heterogeneity is a common feature of solid tumor, especially for GBM. EGFRvIII is heterogeneously expressed on glioblastoma cells in vivo. Therefore, there is a risk of tumor progression due to the lack of this antigen.[48] EGFRvIII was first tested in a phase II clinical trial ACTIVATE, and subsequently followed up with two additional phase II trials, ACT II and ACT III. These three uncontrolled phase II trials focused in rindopepimut vaccination in selected patients with gross total resection and no evidence of progression after adjuvant chemoradiotherapy. They have shown the evidence of better progression-free survival of 15 months and median survival of 24 months compared with historical controls.[101-103] ACT IV is an international, randomized, double-blind phase III clinical trial that examined whether rindopepimut plus standard treatment would prolong overall survival in GBM patients with minimal residual disease (MRD). MRD was defined as the presence of <2 cm2 of enhancing tumor tissue after surgery and chemoradiotherapy. Around 370 patients were randomized into each arm to receive either rindopeptimut or keyhole limpet hemocyanin (KLH; the carrier protein in rindopepimut). At the final analysis, there was no significant difference in overall survival between the rindopeptimut and control group for patients with MRD (median 20.1 months in the rindopepimut group versus 20.0 months in the control group; HR 1.01, 95% CI .79–1.30; P = .93).[97]

IDH1 peptide is another molecule that has been investigated in clinical trials. Based on promising results of IDH1 peptide vaccines in preclinical experiments,[104] two ongoing phase I clinical trials (NOA-16 and RESIST) have been started to investigate its efficacy against GBM patients. This vaccine is engineered to specifically target the IDH1R132 H mutation.[105]

Survivin is highly expressed in GBM and other cancers. SurVaxM is a peptide vaccine of amino acids 53–67 of the protein, conjugated with keyhole limpet hemocyanin.[106] A phase II study (NCT02455557) is currently investigating the treatment of 64 newly diagnosed GBM patients with TMZ and the SurVaxM vaccine. (Survaxm Vaccine Therapy and Temozolomide in Treating Patients With Newly Diagnosed Glioblastoma. Available at: https://ClinicalTrials.gov/show/NCT02455557.) Early results indicate an improved PFS and OS compared to historical controls.[107] A phase I clinical trial (NCT02507583) is investigating the use of an antisense oligodeoxynucleotide against insulin-like growth factor (IGF) type I receptor (IMV-001) for treatment of 33 newly diagnosed glioblastoma. The results of this clinical trial indicated that IGV-001 was well tolerated with an improved PFS compared with standard-of-care.[108] In an earlier phase I personalized protein vaccine (PPV) immunotherapy trial of 12 recurrent GBM patients who were temozolomide-refractory, the researchers found that PPV monotherapy was safe and active in suppressing cancer progression and may extend patients survival by enhancing immunoreactivity.[109] In a randomized, double-blind, phase III trial, 88 HLA-A24-positive GBM patients refractory to temozolomide-based therapy were randomly assigned to receive PPV treatment (58 patients) or best supportive care (BSC; 30 patients). Four peptides chosen from 12 peptide candidates based on pre-vaccination IgG levels specific to each peptide or four corresponding placebos were injected subcutaneously once weekly for 12 times at the first course, followed by biweekly vaccinations until disease progression. However, the results of this trial were unfavorable. The primary endpoint of OS was not met in this clinical trial. Median OS was 8.4 months with PPV and 8 months with BSC.[99]

Neoantigens are identified by whole exome DNA and RNA sequencing, which are resulted from somatic DNA mutations including nonsynonymous point mutations, insertions or deletions, gene fusions and frameshift mutations.[110] Neoantigens are a promising and more personalized cancer treatment approach. Two clinical trials have demonstrated the potential of personalized GBM vaccination.[111,112] Three vaccines (APVAC1, APVAC2, and NeoVax) were investigated: 2 (APVAC1 and APVAC2) in the GAPVAC trial and 1 (NeoVax) by Keskin et al. In the GAPVAC study, 16 newly diagnosed GBM patients received two synthesized vaccines, one aimed at unmutated peptides (APVAC1) and the other aimed at neoantigens (APVAC2). In 11 patients, CD4+ and CD8+ T cell response were observed to APVAC1 and APVAC2. However, there are some differences of immunogenicity between these two vaccines. APVAC1 induced 50% immunogenicity while APVAC2 induced 84.7% immunogenicity. APVAC1 elicited mainly CD8+ T cell responses and APVAC2 produced primarily CD4+ T cell responses. The efficacy of these two vaccines was encouraging for which the median PFS and OS was 14.5 and 29 months, respectively.[111] In another neoantigen vaccine clinical study, 8 patients with newly diagnosed and MGMT unmethylated GBM received only a neoantigen vaccine (NeoVax). Two patients after receiving NeoVax treatment showed immunogenicity and both types of responses of CD4+ T cells and CD8+ T cells were observed. For survival, A median PFS of 7.6 months and median OS of 16.8 months was reported.[112] DCVax-L is a personalized approach to peptide vaccination that uses autologous, or patient-derived, DCs pulsed with resected tumor lysate to target a variety of tumor antigens. In a phase III trial (NCT00045968) analyzing DCVax-L, it showed great potential for this vaccination strategy when combined with standard therapy for a newly diagnosed GBM.[98] Some studies explored the feasibility of mRNA-transfected DC vaccines. The mRNA-transfected DCV was suggested to be safe and well-tolerated. Compared to matched controls, progression-free survival (PFS) was 2.9 times longer in vaccinated patients (NCT00846456).[113] In a phase II clinical trial, autologous DCs were generated from peripheral blood monocytes and pulsed with autologous whole tumor lysate. This tumor lysate-pulsed DC vaccines in combination with standard chemoradiotherapy was proved feasible and safe in newly diagnosed GBM patients (NCT01006044).[114] However, in a multicentric randomized open-label phase II study, vaccination with tumor lysate-charged autologous DCs (Audencel) could not improve the clinical outcomes in newly diagnosed GBM patients.[115] AV-GBM-1, which are autologous DCs loaded with TAAs from a short-term cell culture of autologous tumor cells, are given to newly diagnosed GBM patients to evaluate overall survival in an ongoing phase II clinical trial. (NCT03400917).

Dendritic cells (DCs) are antigen presenting cells that can traffic via the tumor draining lymph nodes of the brain to the deep cervical lymph nodes and promote an adaptive antitumor immune response.[116] Therefore, DCs are an ideal cell type to develop cellular vaccination against tumors. In preclinical models and early-stage clinical trials, DC vaccinations have shown the effectiveness against gliomas.[117,118]

A phase I/II clinical trial enrolled 24 patients with recurrent malignant glioma. This trial investigated the use of a DC therapy that was generated with granulocyte macrophage colony-stimulating factor and interleukin 4 with or without OK-432. Dendritic cells were injected intradermally, or both intratumorally and intradermally. This clinical trial demonstrated the tolerance of DC vaccines with no observed adverse events or radiographic evidence of autoimmune reactions. The overall survival of patients with GBM was 480 days which was significantly longer than that in the control group. Moreover, the patients with both intratumoral and intradermal administrations had a better survival time than patients with intradermal administration only. In addition, there was an increased T cell reactivity after DC vaccination.[119]

ICT-107 is another DC-based vaccine that was specifically designed for newly diagnosed GBM patients. This vaccine consists of DCs incubated ex vivo with TAAs expressed in GBM cells including HER2, IL-13 receptor subunit-α2 (IL-13 Rα2), melanoma-associated antigen 1 (MAGEA1), interferon-inducible protein AIM2, L-dopachrome tautomerase (DCT) and melanocyte protein (PMEL). The phase I clinical trial of ICT-107 enrolled 20 GBM patients and confirmed the safety. The median PFS was 16.9 months and median OS was 38.4 months in the newly diagnosed GBM patients.[120] In a double-blind, placebo-controlled phase II clinical trial, the safety and efficacy of ICT-107 were investigated for patients with newly diagnosed GBM. In this trial, 124 GBM patients were randomly assigned to receive ICT-107 or autologous DCs that were not exposed to the TAAs of GBM. Although the overall survival was not significantly improved, ICT-107 has therapeutic activity in HLA-A2-positive patients.[121] A randomized, double-blind phase III clinical trial of ICT-107 (NCT02546102) investigated the efficacy of ICT-107 compared to the standard-of-care. However, this study was suspended before achieving the primary endpoint due to a lack of funding.[98]

Immune checkpoint inhibitors

Immune checkpoint inhibitors (ICIs) are monoclonal antibodies that decrease the activity of negative regulatory pathways that limit T cell activation by targeting surface receptors called immune checkpoints.[122,123] Under physiological conditions, immune checkpoint molecules can lower cytotoxic T-cell function, whereas when the immune checkpoint is abnormally activated via ICIs, suppression of tumor immune response occurs and T-cell function is restored, thereby increasing the immunotherapeutic effect. Currently, immune checkpoints are primarily focused on programmed cell death protein 1 (PD-1) and cytotoxic T-lymphocyte-associated protein 4 (CTLA-4) (Table 3).[124,125] Considerable improvements in patient outcomes have been achieved for various challenging tumors such as melanoma, lung cancer and renal cancer by utilizing anti-PD-1 and anti-PD-L1 antibodies.[126-128] CheckMate-143 (NCT02017717), the first randomized phase I clinical trial in recurrent GBM, evaluated the tolerability and efficacy of nivolumab (PD-1 inhibitor) alone or in combination with ipilimumab (CTLA-4 inhibitor). All enrolled patients received surgical resection, radiotherapy, and temozolomide before being split into three treatment arms and a vast majority of patients received subsequent therapy. Interestingly, nivolumab monotherapy resulted in a greater median overall survival (10.4 months vs 9.2 months or 7.3 months) than NIVO1+IPI3 (nivolumab 1 mg/kg + ipilimumab 3 mg/kg) or NIVO3+IPI1 (nivolumab 3 mg/kg + ipilimumab 1 mg/kg). Grade 3 or higher adverse events were observed only when combined inhibition is administered, suggesting the necessity for further investigation.[129] Phase III of this clinical trial enrolled and randomized 369 recurrent GBM patients to receive nivolumab 3 mg/kg or bevacizumab (an antiangiogenic drug targeting VEGF) 10 mg/kg every two weeks until confirmed disease progression. Although median overall survival and toxicity were comparable between nivolumab and bevacizumab treated groups, the latter showed shorter duration of radiologic response.[130] Bevacizumab alone and in combination with irinotecan were evaluated for the efficacy in patients with recurrent GBM in a phase II clinical trial. Despite experiencing grade 3 or higher adverse events, both treatment arms were well tolerated with the median overall survival of 9.2 months and 8.7 months, respectively.[131] Currently, the CheckMate-548 (NCT02667587) and the CheckMate-498 (NCT02617589) are two ongoing phase III trials investigating nivolumab as a potential treatment for patients with glioblastoma that is MGMT-unmethylated. CheckMate-548 compares temozolomide plus radiation therapy combined with nivolumab or placebo, while CheckMate-498 compares nivolumab vs temozolomide each in combination with radiation therapy.

Table 3.

Summary of immune checkpoint inhibitors used in clinical trials.

Trial name (ClinicalTrials.gov Identifier)	Treatment	Phase of trial	Number of participants	Primary end point or outcomes	Summary of results
NCT02017717	Nivolumab vs. bevacizumab	III	530	OS	Median OS 9.5 months vs 9.8 months
NCT02617589	Nivolumab vs. temozolomide in combination with radiation therapy	III	560	OS	Median OS 13.4 months vs 14.88 months
NCT02667587	Temozolomide + radiation therapy in combination with nivolumab or placebo	III	716	PFS and OS	No survival advantage over placebo
NCT04606316	Nivolumab in combination with ipilimumab and surgery	I	60	Tumor infiltrating T lymphocyte density and safety	Ongoing study, estimated completion date 12/2022
NCT03743662	Nivolumab with radiation therapy and bevacizumab	II	94	OS	Ongoing study, estimated completion date 11/2022
NCT02550249	Neoadjuvant nivolumab	II	29	Efficacy and safety	Median OS 7.3 months
NCT04396860	Ipilimumab and nivolumab plus radiation therapy	II/III	485	PFS and OS	Ongoing study, estimated completion date 8/2024
NCT02311920	Ipilimumab and/or nivolumab in combination with temozolomide	I	32	DLT	Ongoing study
NCT04145115	Ipilimumab and nivolumab	II	37	ORR	Ongoing study, estimated completion date 5/2023
NCT02337491	Pembrolizumab with or without bevacizumab	II	80	MTD, DLT, and PFS	Median OS 8.8 months together vs 10.3 months for pembrolizumab alone
NCT02054806	Pembrolizumab	I	477	Best overall response	Median OS 14.4 months
NCT02335918	Combination of varlilumab and nivolumab	I/II	175	DLT, ORR, and OS	Study completed, no available info
NCT02336165	Durvalumab monotherapy, with bevacizumab or with radiaotherapy	II	159	OS and PFS	Ongoing study
NCT03673787	Atezolizumab in combination with ipatasertib	I/II	87	DLT	Ongoing study, estimated completion date 7/2022
NCT03961971	Anti-Tim-3 in combination with anti-PD-1 and stereotactic radiosurgery	I	15	Serious adverse events	Ongoing study, estimated completion date 9/2022
NCT02658981	Anti-LAG-3 or urelumab alone and in combination with nivolumab	I	63	MTD	Ongoing study

AEs, adverse events; DLT, dose-limiting toxicity; MTD, maximum tolerated dose; OS, overall survival; PFS, progression-free survival; ORR, objective response rate.

Pembrolizumab, another anti-PD1 checkpoint inhibitor, is currently being investigated as the treatment of gliomas.[132] In a phase II trial, neoadjuvant with pembrolizumab administration prior to surgery in addition to post-surgery adjuvant treatment showed increased survival in patients with recurrent GBM.[133] CTLA-4 is an immune checkpoint that suppresses T cell function by competitively binding to CD80 and CD86.[134] Clinical trials (NCT02311920, NCT02829931) evaluating ipilimumab therapies are still ongoing. LAG-3 is another immune checkpoint receptor that inhibits T-cell activity while promoting the suppressive activity of Tregs.[135] A phase I trial (NCT02658981) evaluating BMS -986,016 (LAG-3 inhibitor) alone and in combination with nivolumab in recurrent GBM patients is underway. TIM-3, another receptor expressed on lymphocytes that can induce T-cell exhaustion and suppress immune response, can lead to a poor prognosis.[136] A phase I trial (NCT03961971) studying the side effects of stereotactic radiosurgery with MBG453 (TIM-3 inhibitor) and spartalizumab (PD-1 inhibitor) therapy is still in progress.

Limitations

Clinical advances and breakthrough in immunotherapy for other tumors have inspired treatment for GBM from an immunotherapeutic angle. However, GBM presents unique challenges with characteristics including: (1) the BBB that limits the permeability for drug delivery, (2) microglia, TAMs and MDSCs contributing to the immunosuppressive microenvironment, (3) limited cytotoxic T cell activation and function, (4) low mutational burden and limited neoantigen profile. Current explorations in CAR T cells, OVs, vaccines, and immune checkpoint inhibitors have yet to show improvements in survival outcomes. In recurrent presentations, since CAR T cells operate by antigen presentation for T cell activation, CAR T efficacy was limited due to the adaptive resistance of GBM, leading to antigen loss as well as T cell exhaustion. Despite the broad targeting capabilities of vaccines, their applications are mainly affected by the limited somatic mutations of GBM cells, thus making antigen escape a concern. In the application of OVs, achieving sufficient replication for GBM apoptosis without triggering an excessive inflammatory response that leads to early elimination has been greatly challenging. Immune checkpoint inhibitors have been disappointing in GBM, possibly due to inadequate tumor-infiltrating lymphocytes with the presence of excessive Tregs and MDSCs, resulting in unfavorable downstream checkpoint blockade effects.[137]

Discussion

Immunotherapy has revolutionized cancer care across various tumor types, but failed to generate comparable clinical results for GBM. Here, we introduced basic knowledge underlying immune targeting and promising immunotherapeutic strategies including CAR T cells, OVs, cancer vaccines, and checkpoint blockade inhibitors that have been recently investigated in glioblastoma. As mentioned, GBM cells is presented with a low mutational burden with certain antigen targets being selectively downregulated or not essential for survival, thus providing few therapeutic targets for the immune system.[134] GBM’s intratumoral molecular heterogeneity, rapid growth rate, as well as immunosuppressive microenvironment also contribute to the unique challenges when taking an immunotherapeutic approach. Furthermore, significant immunoediting causing an evolution in GBM’s molecular profile can possibly result in an overly suppressive and evasive tumor. This phenomenon creates epitopes that limit the recognition of CAR T cells, thereby resulting in a declining antitumor effect over time. Targeting TAMs and Tregs of the TME has been investigated by inhibition of CSF-1 (NCT02526017) and TGFβ (NCT02423343), hoping for clinical benefits but to no avail.[31] Given such findings, it might be possible that tumors present themselves differently in different patients and their susceptibility to immunotherapy may vary from case to case. Identifying which patients are more susceptible can be greatly beneficial for generating a robust response.[138] Patients with higher mutation loads suggest higher levels of neoantigens, which may improve the success rate of current immunotherapeutic strategies. Therefore, targeting neoantigens that are absent on healthy tissue while being essential for tumor survival across various GBM subtypes is of great importance. A well-established research design is also crucial to ensure that maximal information can be obtained from every clinical trial, while not exposing patients to futile treatments.

Moreover, supportive treatments including high-dose steroids and chemotherapies contribute to immunosuppression and lymphopenia.[139,140] T-cell sequestration in bone marrow also leads to a tumor-adaptive mode of immunocompetent cells dysfunction in the setting of GBM.[141] In addition, continual interaction with antigens is likely to induce T-cell exhaustion.[142] Together, there is no development of an efficacious or durable antitumor immune response.

Finally, utilizing different immunotherapeutic strategies as combinatory therapies are being actively investigated, yet more than half of the patients with responsive GBM fail to derive clinical benefits. Therefore, immune-oncology research is gradually being directed toward development of strategiesto bypass the tumor resistance mechanisms, including intrinsic resistance (stops the initiation of a response), adaptive resistance (deactivates tumor-infiltrating immune cells) and acquired resistance (protects tumor cells from destruction when attacked by the immune system). This highlights the requirement for an in-depth understanding of the interactions between GBM and the immune system.[6]

Future prospects

Many current immunotherapeutic strategies are expanding the variety of antigens targeted and modulating the TME to avoid or tackle various mechanisms of resistance. While many advances have been made in the field, there has not been a breakthrough in clinical trials. CAR T therapy should find a way to overcome GBM heterogeneity by engineering multiple antigen specific CAR T cells. ”Off-the-shelf” allogeneic CAR T cells is a promising option such as immediate availability of cryopreserved batches for treatment without requiring the time to manufacture and delay treatment.

However, graft-versus-host disease and quick elimination by the host immune system are issues that need to be addressed in the future development.[143] Over the recent years, viral therapy incorporating new genetic constructs that directly involve the protein expression machinery have seen promising results, though uptake efficiencies and larger clinical trials are still issues to be addressed. Vaccine-based immunotherapy proceeds to produce encouraging studies while moving forward to evaluate the durability of antigen combinations. Rapid and enhanced immunogenicity of these treatments as well as individualized vaccines are potentially becoming important. In order to substantially impact clinical outcomes, immune checkpoint inhibitors may require downregulation of counterproductive cytokines and T cell population shifting by certain treatments. Future GBM treatment will likely involve combined approaches with synergistic effects to not only target the tumor but also the reverse the TME suppression as well as preventing antigen escape.

Conclusions

In summary, while the exploration of immunotherapy has dramatically improved the prognosis for numerous types of advanced solid tumors, GBM has demonstrated strong resistance mechanisms. Future combinatory therapies are likely to be delivered at different stages throughout the immunosuppressive cycle and target each tumor resistance mechanisms concurrently to achieve tumor regression. As the search for novel tumor-associated and tumor-specific antigens continues, new discoveries and advancements in therapeutic modalities also boost efficacy and reduce toxicity, conjointly contributing to the clinical efficacy of immunotherapies.