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Updated: Dec 18, 2025

Therapy Testing in a Spheroid-based 3D Cell Culture Model for Head and Neck Squamous Cell Carcinoma
Published on: April 20, 2018
[FGFR-targeted therapy in head and neck carcinomas]
1Klinik und Poliklinik für Hals-Nasen-Ohrenheilkunde/Chirurgie, Universitätsklinikum Bonn, Venusberg-Campus 1, 53127, Bonn, Deutschland. dimo.dietrich@gmail.com.
Background:
Genomic aberrations (mutations, gene fusions, amplifications) and dysregulation of the fibroblast growth factor (FGF) receptor (FGFR) signaling pathway are frequently found in squamous cell carcinomas of the head and neck (HNSCCs). Targeted therapy with tyrosine kinase inhibitors (TKIs) or monoclonal antibodies directed against FGF receptors therefore represents a promising approach for the treatment of HNSCC.
Objective:
This review article describes the current status of FGFR-directed therapies for head and neck tumors (especially HNSCC) and, in this context, discusses genomic alterations of the FGFR pathway as potential companion predictive biomarkers.
Methods:
This article is based on searches of PubMed, ClinicalTrials.gov, and conference proceedings.
Results:
First results prove the efficacy of TKIs both in HNSCC and in adenocarcinomas of the head and neck, especially in thyroid and adenocystic salivary gland carcinomas.
Conclusion:
Early clinical and preclinical data point to the promise of biomarker-directed treatment of patients with head and neck tumors using FGFR-targeted TKIs.
Insights
Targeted therapies using fibroblast growth factor (FGF) receptor (FGFR) inhibitors show promise for head and neck cancers. Genomic alterations in FGFR signaling can serve as biomarkers to guide treatment decisions for patients with these tumors.
Area of Science:
- Oncology
- Genetics
- Pharmacology
Background:
- Genomic aberrations and fibroblast growth factor (FGF) receptor (FGFR) pathway dysregulation are common in head and neck squamous cell carcinomas (HNSCCs).
- Targeted therapies, including tyrosine kinase inhibitors (TKIs) and monoclonal antibodies against FGFRs, offer a promising treatment strategy for HNSCC.
Purpose of the Study:
- To review the current status of FGFR-directed therapies for head and neck tumors, with a focus on HNSCC.
- To discuss the role of FGFR pathway genomic alterations as potential companion predictive biomarkers for these therapies.
Main Methods:
- Literature search of PubMed, ClinicalTrials.gov, and conference proceedings.
- Review and synthesis of existing data on FGFR-targeted therapies and biomarkers in head and neck cancers.
Main Results:
- Early results indicate that TKIs are effective in treating HNSCC and other head and neck adenocarcinomas, including thyroid and adenocystic salivary gland carcinomas.
- FGFR-targeted TKIs demonstrate efficacy in preclinical and early clinical studies.
Conclusions:
- Biomarker-directed treatment using FGFR-targeted TKIs holds significant promise for patients with head and neck tumors.
- Further clinical investigation is warranted to fully establish the efficacy and predictive value of FGFR alterations in guiding HNSCC treatment.
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