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Updated: Aug 20, 2026

Therapy Testing in a Spheroid-based 3D Cell Culture Model for Head and Neck Squamous Cell Carcinoma
Published on: April 20, 2018
Novel therapeutic targets in squamous cell carcinoma of the head and neck
1Department of Medicine, Section of Hematology/Oncology, University of Chicago, 5841 S. Maryland Avenue, Chicago, IL 60637-1470, USA. ecohen@medicine.bsd.uchicago.edu
Abstract:
The treatment of squamous cell carcinoma of the head and neck (SCCHN) has recently witnessed the introduction of molecularly targeted agents based on disease biology, target discovery, and validation. One class of agents, the epidermal growth factor receptor (EGFR) inhibitors, is currently in phase III trials. There are multiple processes, however, that appear to be suitable for targeted therapy beyond EGFR. These include signal transduction, cell cycle control, prostaglandin synthesis, protein degradation, hypoxia, and angiogenesis. These systems and specific protein targets will be reviewed in detail with emphasis on promising preclinical and early clinical evidence of activity.
Insights
New targeted therapies are emerging for squamous cell carcinoma of the head and neck (SCCHN). Beyond epidermal growth factor receptor (EGFR) inhibitors, other molecular targets show promise for SCCHN treatment.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Squamous cell carcinoma of the head and neck (SCCHN) treatment is evolving with targeted therapies.
- Epidermal growth factor receptor (EGFR) inhibitors represent a key class of agents currently in late-stage clinical trials.
Purpose of the Study:
- To review potential molecular targets for SCCHN therapy beyond EGFR.
- To highlight promising preclinical and clinical evidence for novel targeted agents.
Main Methods:
- Literature review of molecular pathways implicated in SCCHN.
- Analysis of preclinical and early clinical data for targeted agents.
- Focus on signal transduction, cell cycle control, prostaglandin synthesis, protein degradation, hypoxia, and angiogenesis.
Main Results:
- Several molecular pathways beyond EGFR are viable targets for SCCHN treatment.
- Promising preclinical and early clinical data exist for agents targeting these pathways.
- EGFR inhibitors are advancing, but other targets offer therapeutic potential.
Conclusions:
- Targeted therapy for SCCHN can extend beyond EGFR inhibition.
- Further research into novel molecular targets and agents is warranted.
- These findings may guide future development of SCCHN treatments.
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