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Profiling Sensitivity to Targeted Therapies in EGFR-Mutant NSCLC Patient-Derived Organoids
Published on: November 22, 2021
Current and emerging EGFR therapies for glioblastoma
Stefan Alexandru Artene1, Cristian Tuţă1, Alexandra Dragoi1
1a Department of Functional Sciences , University of Medicine and Pharmacy of Craiova, Craiova, Romania.
Abstract:
Glioblastomas (GBMs) are the most lethal and hard to treat malignancies in clinical practice. The standard of care for treating GBM involving surgery and adjuvant radiotherapy and concomitant temozolomide (TMZ) has remained virtually unchanged in the past decade. Molecular targeted therapies against cancer-specific structures have reported mediocre results in the treatment of GBM, due to multiple factors such as the presence of the blood brain barrier or a vast array of molecular alterations which greatly hinder the action of the most therapeutic agents. One such therapy is directed against the epidermal growth factor (EGF) and its' receptor (EGFR) using either monoclonal antibodies or tyrosine kinase inhibitors. Even though anti-EGF/EGFR treatment produced encouraging results in other forms of cancer it failed to present any clinical benefit for patients with GBM. Lately, immunotherapies that focus on using the host's own immune system against cancer cells have gained popularity, with approaches like peptide vaccination being successfully used in clinical trials for different types of malignancies. These immune-based therapies could hold the key to improving both the prognosis and quality of life for patients suffering for cancers previously considered incurable, such as GBM.
Insights
Glioblastomas (GBMs) remain challenging to treat despite standard therapies. Immunotherapies, like peptide vaccination, show promise for improving outcomes in GBM patients.
Area of Science:
- Neuro-oncology
- Cancer immunology
Background:
- Glioblastomas (GBMs) are aggressive brain tumors with poor prognoses.
- Current standard treatments (surgery, radiation, temozolomide) offer limited efficacy.
- Targeted therapies, including anti-EGFR/EGF, have shown minimal clinical benefit in GBM due to biological complexities.
Purpose of the Study:
- To review the limitations of current GBM treatments.
- To explore the potential of immunotherapies, specifically peptide vaccination, for GBM treatment.
Main Methods:
- Literature review of glioblastoma treatment strategies.
- Analysis of targeted therapy outcomes in GBM.
- Evaluation of emerging immunotherapy approaches in oncology.
Main Results:
- Standard GBM care has seen little advancement.
- Targeted therapies targeting EGF/EGFR pathways have failed to improve GBM patient outcomes.
- Immunotherapies, such as peptide vaccination, are emerging as promising strategies.
Conclusions:
- Novel therapeutic approaches are urgently needed for glioblastomas.
- Immunotherapy, particularly peptide vaccination, represents a potential paradigm shift for treating GBM.
- Harnessing the host immune system may offer improved survival and quality of life for GBM patients.
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