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Updated: Aug 27, 2025

A Model for Perineural Invasion in Head and Neck Squamous Cell Carcinoma
Published on: January 5, 2017
STING Agonists in Head and Neck Squamous Cell Carcinoma
David G Wallington1, Joseph N Contessa, Thomas J Hayman
1From the Department of Therapeutic Radiology, Yale School of Medicine, New Haven, CT.
Stimulator of interferon genes (STING) agonists show promise for head and neck squamous cell carcinoma (HNSCC). Combining STING activation with DNA-damaging agents, rather than monotherapy, may improve patient outcomes.
Area of Science:
- Oncology
- Immunology
- Pharmacology
Background:
- Head and neck squamous cell carcinoma (HNSCC) presents significant therapeutic resistance.
- The Stimulator of interferon genes (STING) pathway is crucial for antitumor responses.
- STING agonists are being developed as targeted therapies for HNSCC.
Purpose of the Study:
- To review preclinical and clinical data on STING agonists in HNSCC.
- To explore the potential of STING pathway activation in HNSCC treatment.
- To identify strategies for enhancing STING agonist efficacy.
Main Methods:
- Review of preclinical studies on STING agonists in HNSCC models.
- Analysis of clinical trial data for STING agonists in HNSCC.
- Evaluation of combination therapy approaches involving STING agonists.
Main Results:
- STING agonists demonstrate preclinical efficacy as single agents and with PD-1 inhibitors.
- Clinical efficacy of STING agonists as monotherapy in HNSCC has been limited.
- Preclinical data suggest enhanced efficacy when STING agonists are combined with DNA-damaging agents.
Conclusions:
- STING pathway activation is a promising therapeutic target for HNSCC.
- Combination therapy with STING agonists and DNA-damaging agents warrants further investigation.
- Optimizing STING agonist use may overcome therapeutic resistance in HNSCC.
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Published on: April 22, 2019
06:11Therapy Testing in a Spheroid-based 3D Cell Culture Model for Head and Neck Squamous Cell Carcinoma
Published on: April 20, 2018
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