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Immunotherapy Resistance in Glioblastoma
Open accessAbstract
Glioblastoma is the most common malignant primary brain tumor in adults. Despite treatment consisting of surgical resection followed by radiotherapy and adjuvant chemotherapy, survival remains poor at a rate of 26.5% at 2 years. Recent successes in using immunotherapies to treat a number of solid and hematologic cancers have led to a growing interest in harnessing the immune system to target glioblastoma. Several studies have examined the efficacy of various immunotherapies, including checkpoint inhibitors, vaccines, adoptive transfer of lymphocytes, and oncolytic virotherapy in both pre-clinical and clinical settings. However, these therapies have yielded mixed results at best when applied to glioblastoma. While the initial failures of immunotherapy were thought to reflect the immunoprivileged environment of the brain, more recent studies have revealed immune escape mechanisms created by the tumor itself and adaptive resistance acquired in response to therapy. Several of these resistance mechanisms hijack key signaling pathways within the immune system to create a protumoral microenvironment. In this review, we discuss immunotherapies that have been trialed in glioblastoma, mechanisms of tumor resistance, and strategies to sensitize these tumors to immunotherapies. Insights gained from the studies summarized here may help pave the way for novel therapies to overcome barriers that have thus far limited the success of immunotherapy in glioblastoma.
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“GBM immunoresistance may also be acquired in response to therapy, through changes in checkpoint expression, epigenetic changes, and loss of tumour antigen expression [10].”
From Preclinical development of an mRNA-based multiepitope immunotherapeutic for glioblastoma (2025) · cites this paper as [10]
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“Tumour cell heterogeneity and an immunosuppressive microenvironment contribute to primary GBM immunoresistance, which dampens anti-tumour responses by macrophages and T cells [7, 10].”
From Preclinical development of an mRNA-based multiepitope immunotherapeutic for glioblastoma (2025) · cites this paper as [10]
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Items 201–267 of 267
gp96—The immune system's Swiss army knife
Schild, H., & Rammensee, H. (2000) · Nature Immunology · doi:10.1038/77770 · Cited by 91
Proteolytic Disassembly Is a Critical Determinant for Reovirus Oncolysis
Alain, T., Kim, T. S. Y., Lun, X., Liacini, A., Schiff, L. A., Senger, D. L., & Forsyth, P. A. (2007) · Molecular Therapy · doi:10.1038/sj.mt.6300207 · Cited by 89
Sakai, K., Shimodaira, S., Maejima, S., Udagawa, N., Sano, K., Higuchi, Y., Koya, T., Ochiai, T., Koide, M., Uehara, S., et al. (2015) · Journal of neurosurgery · doi:10.3171/2015.1.jns141554 · Cited by 88
Ipilimumab and Bevacizumab in Glioblastoma
Carter, T. J., Shaw, H. M., Cohn-Brown, D., Chester, K. A., & Mulholland, P. J. (2016) · Clinical Oncology · doi:10.1016/j.clon.2016.04.042 · Cited by 84
Prognostic significance of IDH mutation in adult low-grade gliomas: a meta-analysis
Sun, H., Yin, L.-H., Li, S., Han, S., Song, G., Liu, N., & Yan, C. (2013) · Journal of Neuro-Oncology · doi:10.1007/s11060-013-1107-5 · Cited by 83
The CNS and the Brain Tumor Microenvironment: Implications for Glioblastoma Immunotherapy
Desland, F. A., & Hormigo, A. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21197358 · Cited by 82
van den Bossche, W. B. L., Kleijn, A., Teunissen, C. E., Voerman, J. S. A., Teodósio, C., Noske, D. P., van Dongen, J. J. M., Dirven, C. M. F., & Lamfers, M. L. M. (2018) · Neuro-Oncology · doi:10.1093/neuonc/noy082 · Cited by 78
Schneider, T., Gerhards, R., Kirches, E., & Firsching, R. P. (2001) · Journal of Neuro-Oncology · doi:10.1023/a:1011856406683 · Cited by 76
Ji, N., Zhang, Y., Liu, Y., Xie, J., Wang, Y., Hao, S., & Gao, Z. (2018) · JCI Insight · doi:10.1172/jci.insight.99145 · Cited by 76
Reardon, D. A., Schuster, J. M., Tran, D. D., Fink, K., Nabors, B., Li, G., Bota, D. A., Lukas, R. V., Desjardins, A., Ashby, L. S., et al. (2015) · Journal of Clinical Oncology · doi:10.1200/jco.2015.33.15_suppl.2009 · Cited by 74
Pollack, I. F., Jakacki, R. I., Butterfield, L. H., Hamilton, R. L., Panigrahy, A., Normolle, D. P., Connelly, A. K., Dibridge, S., Mason, G. E., Whiteside, T. L., et al. (2016) · Journal of Neuro-Oncology · doi:10.1007/s11060-016-2245-3 · Cited by 71
Rolan, P. E., Gibbons, J. A., He, L., Chang, E., Jones, D., Gross, M. I., Davidson, J. B., Sanftner, L. M., & Johnson, K. W. (2008) · British Journal of Clinical Pharmacology · doi:10.1111/j.1365-2125.2008.03270.x · Cited by 70
Ma, H.-I., Chiou, S., Hueng, D., Tai, L.-K., Huang, P., Kao, C.-L., Chen, Y., & Sytwu, H. (2010) · Journal of neurosurgery · doi:10.3171/2009.11.jns091396 · Cited by 68
Anti‐angiogenesis and metastasis: a tumour and stromal cell alliance
Moserle, L., & Casanovas, O. (2013) · Journal of Internal Medicine · doi:10.1111/joim.12018 · Cited by 66
Rainov, N. G., Kramm, C. M., Banning, U., Riemann, D., Holzhausen, H., Heidecke, V., Burger, K. J., Burkert, W. L., & Körholz, D. (2000) · Gene Therapy · doi:10.1038/sj.gt.3301311 · Cited by 65
Cancer immunotherapy: moving forward with peptide T cell vaccines
Kumai, T., Fan, A. E., Harabuchi, Y., & Celis, E. (2017) · Current Opinion in Immunology · doi:10.1016/j.coi.2017.07.003 · Cited by 64
Recombinant Poliovirus for Cancer Immunotherapy
Gromeier, M., & Nair, S. K. (2018) · Annual Review of Medicine · doi:10.1146/annurev-med-050715-104655 · Cited by 59
Wang, X., Kazim, L., Repasky, E. A., & Subjeck, J. R. (2003) · International Journal of Cancer · doi:10.1002/ijc.11058 · Cited by 57
Tumor Selectivity of Oncolytic Parvoviruses: From in vitro and Animal Models to Cancer Patients
Angelova, A. L., Geletneky, K., Nüesch, J. P. F., & Rommelaere, J. (2015) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2015.00055 · Cited by 57
H-1 Parvovirus as a Cancer-Killing Agent: Past, Present, and Future
Bretscher, C., & Marchini, A. (2019) · Viruses · doi:10.3390/v11060562 · Cited by 57
Patel, M. A., Kim, J. E., Theodros, D., Tam, A. J., Velarde, E., Kochel, C. M., Francica, B. J., Nirschl, T. R., Ghasemzadeh, A., Mathios, D., et al. (2016) · Journal for ImmunoTherapy of Cancer · doi:10.1186/s40425-016-0132-2 · Cited by 56
Modulation of the Intratumoral Immune Landscape by Oncolytic Herpes Simplex Virus Virotherapy
Yin, J., Markert, J. M., & Leavenworth, J. W. (2017) · Frontiers in Oncology · doi:10.3389/fonc.2017.00136 · Cited by 55
Brown, N. F., Ng, S., Brooks, C., Coutts, T., Holmes, J., Roberts, C., Elhussein, L., Hoskin, P., Maughan, T., Blagden, S. P., et al. (2020) · BMC Cancer · doi:10.1186/s12885-020-6624-y · Cited by 55
Huang, T., Hlavatý, J., Ostertag, D. G., Espinoza, F. L., Martin, B., Petznek, H., Rodriguez-Aguirre, M. E., Ibañez, C. E., Kasahara, N., Günzburg, W. H., et al. (2013) · Cancer Gene Therapy · doi:10.1038/cgt.2013.51 · Cited by 53
Sampson, J. H., Omuro, A. M. P., Preusser, M., Lim, M., Butowski, N. A., Cloughesy, T. F., Strauss, L. C., Latek, R. R., Paliwal, P., Weller, M., et al. (2016) · Journal of Clinical Oncology · doi:10.1200/jco.2016.34.15_suppl.tps2079 · Cited by 53
Tabatabaei, P., Visse, E., Bergström, P., Brännström, T., Siesjö, P., & Bergenheim, A. T. (2016) · Journal of Neuro-Oncology · doi:10.1007/s11060-016-2271-1 · Cited by 52
Glioblastoma Immunotherapy Targeting the Innate Immune Checkpoint CD47-SIRPα Axis
Hu, J., Xiao, Q., Dong, M., Guo, D., Wu, X., & Wang, B. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.593219 · Cited by 51
Reardon, D. A., Kaley, T. J., Dietrich, J., Clarke, J. L., Dunn, G. P., Lim, M. K., Cloughesy, T. F., Gan, H. K., Park, A. J., Schwarzenberger, P. O., et al. (2019) · Journal of Clinical Oncology · doi:10.1200/jco.2019.37.15_suppl.2032 · Cited by 50
Enhanced immunosuppression by therapy‐exposed glioblastoma multiforme tumor cells
Authier, A., Farrand, K. J., Broadley, K. W. R., Ancelet, L. R., Hunn, M. K., Stone, S., McConnell, M. J., & Hermans, I. F. (2014) · International Journal of Cancer · doi:10.1002/ijc.29309 · Cited by 49
Dendritic cell based vaccination strategy: an evolving paradigm
Filley, A. C., & Dey, M. (2017) · Journal of Neuro-Oncology · doi:10.1007/s11060-017-2446-4 · Cited by 49
Shono, K., Yamaguchi, I., Mizobuchi, Y., Kagusa, H., Sumi, A., Fujihara, T., Nakajima, K., Kitazato, K. T., Matsuzaki, K., Saya, H., et al. (2020) · Scientific Reports · doi:10.1038/s41598-020-71857-3 · Cited by 49
Liu, Y., Chang, Y., He, X., Cai, Y., Jiang, H., Jia, R., & Leng, J. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.01525 · Cited by 47
Jaime‐Ramirez, A. C., Yu, J.-G., Caserta, E., Yoo, J. Y., Zhang, J., Lee, T. J., Hofmeister, C. C., Lee, J. H., Kumar, B., Pan, Q., et al. (2017) · Molecular Therapy — Oncolytics · doi:10.1016/j.omto.2017.05.002 · Cited by 43
Reck, M., Ciuleanu, T., Lee, J.-S., Schenker, M., Audigier-Valette, C., Żurawski, B. A., Linardou, H., Otterson, G. A., Salman, P., Nishio, M., et al. (2021) · Journal of Thoracic Oncology · doi:10.1016/j.jtho.2020.12.019 · Cited by 43
Enhanced phagocytosis of CD47-deficient red blood cells by splenic macrophages requires SHPS-1
Ishikawa-Sekigami, T., Kaneko, Y., Saito, Y., Murata, Y., Okazawa, H., Ohnishi, H., Oldenborg, P., Nojima, Y., & Matozaki, T. (2006) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2006.03.094 · Cited by 42
Anti-GITR therapy promotes immunity against malignant glioma in a murine model
Miska, J. M., Rashidi, A., Chang, A. L., Muroski, M. E., Han, Y., Zhang, L., & Lesniak, M. S. (2016) · Cancer Immunology Immunotherapy · doi:10.1007/s00262-016-1912-8 · Cited by 42
Lang, F. F., Tran, N., Puduvalli, V. K., Elder, J. B., Fink, K., Conrad, C. A., Yung, W. K. A., Peñas-Prado, M., Gomez‐Manzano, C., Peterkin, J. J., et al. (2017) · Journal of Clinical Oncology · doi:10.1200/jco.2017.35.15_suppl.2002 · Cited by 42
Oncolysis by paramyxoviruses: preclinical and clinical studies
Matveeva, O. V., Guo, Z. S., Senin, V. M., Senina, A. V., Shabalina, S. A., & Chumakov, P. M. (2015) · Molecular Therapy — Oncolytics · doi:10.1038/mto.2015.17 · Cited by 41
DNX-2401: an investigational drug for the treatment of recurrent glioblastoma
Philbrick, B. D., & Adamson, D. C. (2019) · Expert Opinion on Investigational Drugs · doi:10.1080/13543784.2019.1694000 · Cited by 41
Adoptive Cell Therapy: A Novel and Potential Immunotherapy for Glioblastoma
Wang, J., Shen, F., Yao, Y., Wang, L., Zhu, Y.-J., & Hu, J. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.00059 · Cited by 40
Effective Treatment of Glioblastoma Multiforme With Oncolytic Virotherapy: A Case-Series
Gesundheit, B., Ben-David, E., Posen, Y., Ellis, R., Wollmann, G., Schneider, E. M., Aigner, K. R., Brauns, L., Neßelhut, T., Ackva, I., et al. (2020) · Frontiers in Oncology · doi:10.3389/fonc.2020.00702 · Cited by 38
Recognizing and managing on toxicities in cancer immunotherapy
Liu, Y., Hui-fang, Y., Dong, S., Zhong, Y., & Hu, S. (2017) · Tumor Biology · doi:10.1177/1010428317694542 · Cited by 37
Xu, L., Xiao, H., Xu, M., Zhou, C., Liang, Y., & Hong, L. (2011) · Journal of Biological Chemistry · doi:10.1074/jbc.m111.292540 · Cited by 36
Mosaheb, M., Dobrikova, E. Y., Brown, M. C., Yang, Y., Cable, J. M., Okada, H., Nair, S. K., Bigner, D. D., Ashley, D. M., & Gromeier, M. (2020) · Nature Communications · doi:10.1038/s41467-019-13939-z · Cited by 36
The double-edge sword effect of anti-CD73 cancer therapy
Stagg, J. (2012) · OncoImmunology · doi:10.4161/onci.1.2.18101 · Cited by 33
Harnessing Radiation Biology to Augment Immunotherapy for Glioblastoma
Rajani, K. R., Carlstrom, L. P., Parney, I. F., Johnson, A. J., Warrington, A. E., & Burns, T. C. (2019) · Frontiers in Oncology · doi:10.3389/fonc.2018.00656 · Cited by 33
Boydell, E., Marinari, E., Migliorini, D., Dietrich, P., Patrikidou, A., & Dutoit, V. (2019) · Cancers · doi:10.3390/cancers11040464 · Cited by 32
Activation of a Helper and Not Regulatory Human CD4+ T Cell Response by Oncolytic H-1 Parvovirus
Moralès, O., Richard, A. S., Martin, N., Mrizak, D., Sénéchal, M., Miroux, C., Pancré, V., Rommelaere, J., Caillet-Fauquet, P., de Launoit, Y., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0032197 · Cited by 31
Bloch, O. G., Shi, Q., Anderson, S. K., Knopp, M. V., Raizer, J. J., Clarke, J. L., Waziri, A. E., Colman, H., Bruce, J. N., Olson, J. J., et al. (2017) · Neuro-Oncology · doi:10.1093/neuonc/nox168.110 · Cited by 31
A virus associated with transplantable human tumors.
Toolan, H. W. (1961) · PubMed · Cited by 30
Adenosinergic Pathway: A Hope in the Immunotherapy of Glioblastoma
Jin, K., Mao, C., Chen, L., Wang, L., Liu, Y., & Yuan, J. (2021) · Cancers · doi:10.3390/cancers13020229 · Cited by 24
Avelumab in newly diagnosed glioblastoma
Jacques, F. H., Nicholas, G. A., Lorimer, I. A. J., Foko, V. S., Prevost, J., Dumais, N., Milne, K., Nelson, B. H., Woulfe, J., Jansen, G. H., et al. (2021) · Neuro-Oncology Advances · doi:10.1093/noajnl/vdab118 · Cited by 24
Window-of-opportunity clinical trial of a PD-1 inhibitor in patients with recurrent glioblastoma.
Groot, J. F. D., Peñas-Prado, M., Mandel, J. J., O'Brien, B. J., Weathers, S.-P. S., Zhou, S., Hunter, K., Alfaro-Munoz, K. D., Fuller, G. N., Huse, J. T., et al. (2018) · Journal of Clinical Oncology · doi:10.1200/jco.2018.36.15_suppl.2008 · Cited by 20
Regulatory T Cells Move in When Gliomas Say “I DO”
Choi, B. D., Fecci, P. E., & Sampson, J. H. (2012) · Clinical Cancer Research · doi:10.1158/1078-0432.ccr-12-2801 · Cited by 19
A phase 2 study of orally administered PLX3397 in patients with recurrent glioblastoma.
Butowski, N. A., Colman, H., Groot, J. F. D., Omuro, A. M. P., Nayak, L., Cloughesy, T. F., Marimuthu, A., Perry, A., Phillips, J. J., West, B. L., et al. (2014) · Journal of Clinical Oncology · doi:10.1200/jco.2014.32.15_suppl.2023 · Cited by 19
Angelova, A. L., Witzens‐Harig, M., Galabov, A. S., & Rommelaere, J. (2017) · Frontiers in Oncology · doi:10.3389/fonc.2017.00093 · Cited by 19
Viral Gene Therapy for Glioblastoma Multiforme: A Promising Hope for the Current Dilemma
Li, J., Wang, W., Wang, J., Cao, Y. B., Wang, S., & Zhao, J. (2021) · Frontiers in Oncology · doi:10.3389/fonc.2021.678226 · Cited by 17
Weathers, S.-P. S., Kamiya-Matsuoka, C., Harrison, R. A., Liu, D. D., Dervin, S., Yun, C., Loghin, M. E., Peñas-Prado, M., Majd, N., Yung, W. K. A., et al. (2020) · Journal of Clinical Oncology · doi:10.1200/jco.2020.38.15_suppl.2511 · Cited by 16
LUMINOS-101: Phase 2 study of PVSRIPO with pembrolizumab in recurrent glioblastoma.
Sloan, A. E., Buerki, R. A., Murphy, C., Kelly, A. T., Ambady, P., Brown, M. C., Butowski, N. A., Cavaliere, R., Curry, W. T., Desjardins, A., et al. (2021) · Journal of Clinical Oncology · doi:10.1200/jco.2021.39.15_suppl.tps2065 · Cited by 16
Clinically Explored Virus-Based Therapies for the Treatment of Recurrent High-Grade Glioma in Adults
Immidisetti, A. V., Nwagwu, C. D., Adamson, D. C., Patel, N. V., & Carbonell, A.-M. (2021) · Biomedicines · doi:10.3390/biomedicines9020138 · Cited by 14
Peereboom, D. M., Nabors, B., Kumthekar, P., Badruddoja, M., Fink, K., Lieberman, F. S., Phuphanich, S., Dunbar, E. M., Walbert, T., Schiff, D., et al. (2018) · Journal of Clinical Oncology · doi:10.1200/jco.2018.36.15_suppl.2058 · Cited by 12
Neyns, B., Salama, L. B., Awada, G., Cremer, J., Schwarze, J. K., Seynaeve, L., Four, S. D., Fischbuch, L., Vanbinst, A., Everaert, H., et al. (2019) · Journal of Clinical Oncology · doi:10.1200/jco.2019.37.15_suppl.2034 · Cited by 11
Brahmer, J. R., Rasco, D. W., Chen, M., Masteller, E. L., Qazi, I., Rogers, S., Sankar, N., Sikorski, R. S., Hambleton, J., & Hodi, F. S. (2016) · Cancer Immunology Research · doi:10.1158/2326-6074.cricimteatiaacr15-b143 · Cited by 9
Combining Ipilimumab and Bevacizumab in Glioblastoma is Really Safe and Effective?
Tini, P., & Pirtoli, L. (2016) · Clinical Oncology · doi:10.1016/j.clon.2016.06.003 · Cited by 5
Avelumab in newly diagnosed glioblastoma multiforme: The SEJ study
Jacques, F. H., Nicholas, G. A., & Lorimer, I. A. J. (2018) · Annals of Oncology · doi:10.1093/annonc/mdy273.393 · Cited by 2
Schwarze, J. K., Bertels, C., Awada, G., Tijtgat, J., Tuyaerts, S., Cras, L., Vaeyens, F., Vanbinst, A., Everaert, H., Michotte, A., et al. (2020) · Annals of Oncology · doi:10.1016/j.annonc.2020.10.553 · Cited by 2
Cancer Stem Cells and Tumor-Associated Macrophages
Zhou, W., & Bao, S. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-803892-5.00014-0 · Cited by 1
Research works printed but not linked: 16
- Bristol-Myers Squibb, 2020, A Randomized Phase 3 Single Blind Study of Temozolomide Plus Radiation Therapy Combined with Nivolumab or Placebo in Newly Diagnosed Adult Subjects with MGMT-Methylated (Tumor O6-Methylguanine DNA Methyltransferase) Glioblastoma
- Bristol-Myers Squibb, 2020, A Randomized, Double-Blind Phase 2/3 Study of Relatlimab Combined with Nivolumab versus Nivolumab in Participants with Previously Untreated Metastatic or Unresectable Melanoma
- DNAtrix, 2021, Announces Positive Data from Phase 2 CAPTIVE (KEYNOTE-192) Study with DNX-2401 in Patients with Recurrent Glioblastoma Highlighted in an Oral Late-Breaking Presentation during Society for Neuro-Oncology (SNO) Annual Meeting
- Hoag Memorial Hospital Presbyterian, 2013, Phase II Trial of Intralesional Adoptive Cellular Therapy of Glioblastoma with Interleukin-2-Stimulated Lymphocytes
- 2021, Inc. A Multicenter Phase 2 Study of Oncolytic Polio/Rhinovirus Recombinant (PVSRIPO) in Recurrent WHO Grade IV Malignant Glioma Patients
- Ludwig Institute for Cancer Research, 2021, Phase 2 Study to Evaluate the Clinical Efficacy and Safety of MEDI4736 in Patients with Glioblastoma (GBM)
- Md Gkf, 2021, Phase II Clinical Trial of HSV G207 with a Single 5 Gy Radiation Dose in Children with Recurrent High-Grade Glioma
- Md Jm, 2021, A Phase 1 Study of M032 (NSC 733972), a Genetically Engineered HSV-1 Expressing IL-12, in Patients with Recurrent/Progressive Glioblastoma Multiforme, Anaplastic Astrocytoma, or Gliosarcoma
- Md Pyw, 2021, A Phase Ib Clinical Trial to Evaluate Early Immunologic Pharmacodynamic Parameters Following Neoadjuvant Anti-PD-1 (Nivolumab), or the Combination of Anti-PD-1 Plus Anti-CTLA-4 (Nivolumab Plus Ipilimumab) in Patients with Surgically Accessible Glioblastoma
- Md Yy, 2021, The Safety and Efficacy Study of Autologous Tumor-Infiltrating T LymphocyteTILnd Transgenic Modified TIL Cells Adoptive Therapies for Patients with Glioblastoma Multiforme
- MediciNova, 2021, Phase 1b/2a Single-Center, Open-Label, Dose Escalation Study to Evaluate the Safety, Tolerability, and Efficacy of MN-166 (Ibudilast) and Temozolomide Combination Treatment in Patients with Newly Diagnosed or Recurrent Glioblastoma
- National Cancer Institute Nci, 2021, A Safety Run-In and Phase II Study Evaluating the Efficacy, Safety, and Impact on the Tumor Microenvironment of the Combination of Tocilizumab, Atezolizumab, and Fractionated Stereotactic Radiotherapy in Recurrent Glioblastoma
- National Cancer Institute (Nci), 2020, Phase I Study of Ipilimumab, Nivolumab, and the Combination in Patients with Newly Diagnosed Glioblastoma
- Pediatric Brain Tumor Consortium, 2016, A Phase I Study of Intratumoral/Peritumoral Herpes Simplex Virus-1 Mutant HSV1716 in Patients with Refractory or Recurrent High Grade Gliomas (HGG)
- Uhscc, 2021, Opens New Trial with PVSRIPO a Viralbased Immunotherapy in Combination with Pembrolizumab
- University of Pennsylvania, 2021, A Phase II Study of the Anti-GITR Agonist INCAGN1876 and the PD-1 Inhibitor INCMGA00012 in Combination with Stereotactic Radiosurgery in Recurrent Glioblastoma
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Metadata
- Authors
- Wang, E. J., Chen, J.-S., Jain, S., Morshed, R. A., Haddad, A. F., Gill, S., Beniwal, A. S., & Aghi, M. K.
- Affiliations
- Brown University (US)
- University of California, San Francisco (US)
- Corresponding author
- Aghi, Manish K.
- ORCID
- Venue
- Frontiers in Genetics
- Publisher
- Frontiers Media SA
- Published
- 2021-12-17
- Volume
- 12
- Pages
- 750675-750675
- ISSN
- 1664-8021 (ISSN-L)
- PMC
- PMC8718605
- OpenAlex
- W4200562336
- Cited by
- 34
- References
- 269
- Citations by year
- 2026: 5 · 2025: 7 · 2024: 8 · 2023: 12 · 2022: 2
- FWCI
- 0.78
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Frontiers in Genetics (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- eScholarship (California Digital Library) (submittedVersion, cc-by)
- Funders
- National Cancer Institute (R01CA227136)
- National Institute of Neurological Disorders and Stroke (R01NS079697)
- Topics
- Health Sciences › Medicine › Oncology › Glioma Diagnosis and Treatment
- Health Sciences › Medicine › Oncology › Cancer Immunotherapy and Biomarkers
- Life Sciences › Immunology and Microbiology › Immunology › Immunotherapy and Immune Responses
- Keywords
- glioblastoma, immunotherapy resistance, immune checkpoint inhibitors, cancer vaccines, adoptive immunotherapy, oncolytic virotherapy, tumor immune evasion, tumor microenvironment, immune privilege, adaptive resistance, radiosensitization
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
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