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Intramucosal Inoculation of Squamous Cell Carcinoma Cells in Mice for Tumor Immune Profiling and Treatment Response Assessment
Published on: April 22, 2019
Anti-EGFR Therapy: Strategies in Head and Neck Squamous Cell Carcinoma
Renato J Oliveira-Silva, Ana Carolina de Carvalho, Luciano de Souza Viana
1Barretos Cancer Hospital, Rua Antenor Duarte Villela, 1331, CEP 14784 400, Barretos, S. Paulo, Brazil. carvalhoal@gmail.com.
Abstract:
Epidermal growth factor receptor (EGFR) is a tyrosine kinase receptor that activates downstream signaling pathways, including the Ras-MEK-Erk and PI3K-AKT pathways, leading to cell proliferation, resistance to apoptosis, angiogenesis and the ability to metastasize. EGFR overexpression is a significant finding in cancer, particularly in head and neck cancer, where it is also associated with a poor prognosis. In recent years, several molecules have been designed to inhibit EGFR activation. Among the many available anti-EGFR drugs, only cetuximab was approved for the treatment of head and neck cancers. However, no predictive biomarkers of cetuximab response are currently known. In the present review, we provide an updated assessment of EGFR biology and its clinical impact in head and neck cancers. A special emphasis is placed on novel patents of EGFR-inhibitors that are anticipated to diversify the anti-EGFR therapies available to treat head and neck cancers. In particular, we outline a new class of irreversible multi-target inhibitors (e.g. afatinib, icotinib, CUDC-101), which may significantly contribute to new head and neck cancer therapies.
Insights
Epidermal growth factor receptor (EGFR) plays a key role in head and neck cancers. New multi-target inhibitors show promise for improving therapies beyond current treatments like cetuximab.
Area of Science:
- Oncology
- Molecular Biology
- Drug Discovery
Background:
- Epidermal growth factor receptor (EGFR) signaling pathways drive cancer progression, including cell proliferation and metastasis.
- EGFR overexpression is common in head and neck cancers, correlating with poor patient prognosis.
- Current anti-EGFR therapies, like cetuximab, are limited by a lack of predictive biomarkers for treatment response.
Purpose of the Study:
- To review the biology and clinical significance of EGFR in head and neck cancers.
- To assess novel EGFR-inhibitor patents and their potential to expand therapeutic options.
- To highlight emerging irreversible multi-target inhibitors for head and neck cancer treatment.
Main Methods:
- Literature review of EGFR biology and its role in head and neck cancer.
- Analysis of recent patents for EGFR-inhibiting molecules.
- Discussion of the clinical implications of novel EGFR inhibitors.
Main Results:
- EGFR activation via Ras-MEK-Erk and PI3K-AKT pathways promotes cancer cell growth and spread.
- Cetuximab is the only approved anti-EGFR drug for head and neck cancers, but its efficacy is not fully predictable.
- New irreversible multi-target inhibitors like afatinib, icotinib, and CUDC-101 represent promising advancements.
Conclusions:
- EGFR remains a critical target in head and neck oncology.
- Novel EGFR inhibitors, particularly multi-target agents, offer potential for more effective and personalized cancer therapies.
- Further research into predictive biomarkers for EGFR-targeted treatments is essential.
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