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EphA3 Pay-Loaded Antibody Therapeutics for the Treatment of Glioblastoma
- Source :
- Cancers, Cancers, Vol 10, Iss 12, p 519 (2018), Volume 10, Issue 12
- Publication Year :
- 2018
-
Abstract
- The EphA3 receptor has recently emerged as a functional tumour-specific therapeutic target in glioblastoma (GBM). EphA3 is significantly elevated in recurrent disease, is most highly expressed on glioma stem cells (GSCs), and has a functional role in maintaining self-renewal and tumourigenesis. An unlabelled EphA3-targeting therapeutic antibody is currently under clinical assessment in recurrent GBM patients. In this study, we assessed the efficacy of EphA3 antibody drug conjugate (ADC) and radioimmunotherapy (RIT) approaches using orthotopic animal xenograft models. Brain uptake studies, using positron emission tomography/computed tomography (PET/CT) imaging, show EphA3 antibodies are effectively delivered across the blood-tumour barrier and accumulate at the tumour site with no observed normal brain reactivity. A robust anti-tumour response, with no toxicity, was observed using EphA3, ADC, and RIT approaches, leading to a significant increase in overall survival. Our current research provides evidence that GBM patients may benefit from pay-loaded EphA3 antibody therapies.
- Subjects :
- 0301 basic medicine
Cancer Research
Antibody-drug conjugate
medicine.medical_treatment
EphA3
lcsh:RC254-282
Article
03 medical and health sciences
0302 clinical medicine
stem cells
Glioma
medicine
medicine.diagnostic_test
biology
business.industry
glioblastoma
lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens
medicine.disease
3. Good health
030104 developmental biology
Oncology
Positron emission tomography
030220 oncology & carcinogenesis
Radioimmunotherapy
Toxicity
Cancer research
biology.protein
radioimmunotherapy
antibody drug conjugate
Antibody
Stem cell
business
Glioblastoma
Subjects
Details
- ISSN :
- 20726694
- Volume :
- 10
- Issue :
- 12
- Database :
- OpenAIRE
- Journal :
- Cancers
- Accession number :
- edsair.doi.dedup.....a2b357de6bcf6c1d31962f06916153f9