Exciting New Advances in Neuro-Oncology: The Avenue to a Cure for Malignant Glioma
Open accessAbstract
Malignant gliomas are the most common and deadly brain tumors. Nevertheless, survival for patients with glioblastoma, the most aggressive glioma, although individually variable, has improved from an average of 10 months to 14 months after diagnosis in the last 5 years due to improvements in the standard of care. Radiotherapy has been of key importance to the treatment of these lesions for decades, and the ability to focus the beam and tailor it to the irregular contours of brain tumors and minimize the dose to nearby critical structures with intensity-modulated or image-guided techniques has improved greatly. Temozolomide, an alkylating agent with simple oral administration and a favorable toxicity profile, is used in conjunction with and after radiotherapy. Newer surgical techniques, such as fluorescence-guided resection and neuroendoscopic approaches, have become important in the management of malignant gliomas. Furthermore, new discoveries are being made in basic and translational research, which are likely to improve this situation further in the next 10 years. These include agents that block 1 or more of the disordered tumor proliferation signaling pathways, and that overcome resistance to already existing treatments. Targeted therapies such as antiangiogenic therapy with antivascular endothelial growth factor antibodies (bevacizumab) are finding their way into clinical practice. Large-scale research efforts are ongoing to provide a comprehensive understanding of all the genetic alterations and gene expression changes underlying glioma formation. These have already refined the classification of glioblastoma into 4 distinct molecular entities that may lead to different treatment regimens. The role of cancer stem-like cells is another area of active investigation. There is definite hope that by 2020, new cocktails of drugs will be available to target the key molecular pathways involved in gliomas and reduce their mortality and morbidity, a positive development for patients, their families, and medical professionals alike.
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Glioblastoma multiforme (GBM) is the most aggressive form of brain tumors/gliomas.
“Glioblastoma multiforme (GBM) is the most aggressive form of brain tumors/gliomas.”
From Potential Therapeutic Effects of Exosomes Packed With a miR-21-Sponge Construct in a Rat Model of Glioblastoma (2019) · cites this paper as [1]
GBM is grade 4 according to the World Health Organization (WHO) classification.
“Glioma is divided into 4 grades and GBM is the grade 4, according to the World Health Organization (WHO) classifications (1).”
From Potential Therapeutic Effects of Exosomes Packed With a miR-21-Sponge Construct in a Rat Model of Glioblastoma (2019) · cites this paper as [1]
Glioblastoma multiforme (GBM) is the most aggressive form of brain tumors, glioma.
“Glioblastoma multiform (GBM) is the most aggressive form of brain tumors, glioma.”
From Potential Therapeutic Effects of Exosomes Packed With a miR-21-Sponge Construct in a Rat Model of Glioblastoma (2019) · cites this paper as [1]
Despite current standard of care combining surgery, radiotherapy and chemotherapy, GBM patients have frequent recurrence and very short life expectancy.
“Despite the current standard of care that combines surgery, radiotherapy and chemotherapy, GBM patients are nonetheless confronted with frequent recurrence, and hence their life expectancy is very short (1, 2, 34).”
From Potential Therapeutic Effects of Exosomes Packed With a miR-21-Sponge Construct in a Rat Model of Glioblastoma (2019) · cites this paper as [1]
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- Authors
- Van Meir, E. G., Hadjipanayis, C. G., Norden, A. D., Shu, H. K., Wen, P. Y., & Olson, J. J.
- Affiliations
- Emory University (US)
- Brigham and Women's Hospital (US)
- Venue
- CA: A Cancer Journal for Clinicians
- Publisher
- Wiley
- Published
- 2010-05-01
- Volume
- 60
- Issue
- 3
- Pages
- 166-193
- ISSN
- 0007-9235 (ISSN-L)
- PMC
- PMC2888474
- OpenAlex
- W2115862526
- Cited by
- 1,372
- References
- 8
- Citations by year
- 2026: 7 · 2025: 33 · 2024: 63 · 2023: 72 · 2022: 93 · 2021: 96 · 2020: 97 · 2019: 100 · 2018: 97 · 2017: 99 · 2016: 80 · 2015: 98 · 2014: 104 · 2013: 97 · 2012: 127
- FWCI
- 47.57
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Locations
- CA A Cancer Journal for Clinicians (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Cancer Institute (CA86335, CA116804, R01CA116804, R01CA086335)
- National Institute of Neurological Disorders and Stroke (NS053454, K08NS053454)
- Topics
- Health Sciences › Medicine › Genetics › Glioma Diagnosis and Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Angiogenesis and VEGF in Cancer
- Health Sciences › Medicine › Reproductive Medicine › Ovarian cancer diagnosis and treatment
- Keywords
- high-grade glioma, glioblastoma, temozolomide, radiotherapy, intensity-modulated radiotherapy, image-guided radiotherapy, fluorescence-guided resection, targeted therapy, anti-angiogenic therapy, bevacizumab, vascular endothelial growth factor, glioma molecular classification, cancer stem-like cells, drug resistance
- MeSH terms
- Antineoplastic Agents, Brain Neoplasms, Epidermal Growth Factor, Glioblastoma, Humans, Molecular Biology, Biomarkers, Tumor, Signal Transduction, Apoptosis, Treatment Failure, Angiogenesis Inhibitors, Receptors, Vascular Endothelial Growth Factor, Vascular Endothelial Growth Factor A
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