Related Experiment Video
Updated: Apr 22, 2026

Quantifying Antibody-Dependent Cellular Cytotoxicity in a Tumor Spheroid Model: Application for Drug Discovery
Published on: April 26, 2024
Quantification of Antibody-Drug Conjugate Targets in Head and Neck Squamous Cell Carcinoma
Mengni He1, Ioannis P Trontzas1, Katherine M Bates2
1Yale University New Haven United States.
Abstract:
Antibody-drug conjugates have shown clinical benefit in common solid tumors like breast cancer, lung cancer, and urothelial cancers, but are just beginning to be investigated in head and neck cancer. We developed a quantitative immunofluorescence (QIF) assay to reproducibly and accurately measure HER3 protein concentrations in formalin fixed, paraffin embedded tissues. Using this assay, we measured HER3 protein concentrations in two head and neck squamous cell carcinoma (HNSCC) tissue microarray cohorts containing 329 patients. Cell lines with mass spectrometry-measured protein concentrations were used to convert fluorescence signals to protein concentrations in amol/mm2. HER3, EGFR, and TROP2 showed a broad dynamic range in our cohorts with almost all of the cases above our assay's LOD. Specifically, 100%, 97.5%, and 98.4% of cases have HER3, EGFR, and TROP2 levels above assay LOD. Interestingly, despite the previous demonstration of extremely low HER2 expression in HNSCC, 39.1% of cases showed HER2 expression above our assay LOD of 52.5 amol/mm2. When comparing between therapeutic targets, 97.2%, 99.3%, and 98.6% of cases are double positive for HER3/EGFR, HER3/TROP2, and EGFR/TROP2, while only, 34.2%, 34.6%, and 30.5% of cases are double positive for HER3/HER2, EGFR/HER2, and TROP2/HER2. HER3, EGFR, and TROP2 are highly expressed in HNSCC. HER2 expression is relatively low in this HNSCC cohort compared to other ADC targets, but there are 39.1% of cases with detectable HER2 exceeding historical estimates. Overall, ADC target levels in HNSCC for approved ADCs suggests that HNSCC patients may benefit from this class of drugs.
Insights
Antibody-drug conjugates show promise for head and neck squamous cell carcinoma (HNSCC). Researchers developed a new assay to measure key protein targets, finding high expression of HER3, EGFR, and TROP2, suggesting potential patient benefit.
Area of Science:
- Oncology
- Molecular Pathology
- Biomarker Discovery
Background:
- Antibody-drug conjugates (ADCs) are effective in solid tumors but under-investigated in head and neck cancer.
- Head and neck squamous cell carcinoma (HNSCC) presents a potential area for ADC therapeutic development.
Purpose of the Study:
- To develop and validate a quantitative immunofluorescence (QIF) assay for measuring HER3 protein in HNSCC tissues.
- To assess the expression levels of HER3, EGFR, TROP2, and HER2 in HNSCC patient cohorts.
Main Methods:
- Development of a QIF assay to quantify HER3 protein in formalin-fixed, paraffin-embedded HNSCC tissues.
- Analysis of two HNSCC tissue microarrays comprising 329 patients.
- Calibration of fluorescence signals to protein concentrations (amol/mm²) using cell lines with mass spectrometry data.
Main Results:
- The QIF assay demonstrated high sensitivity and accuracy for HER3, EGFR, and TROP2, with nearly all cases above the limit of detection (LOD).
- High co-expression rates were observed for HER3/EGFR (97.2%), HER3/TROP2 (99.3%), and EGFR/TROP2 (98.6%).
- While HER2 expression was generally low, 39.1% of cases exceeded the assay LOD, contrary to previous estimates.
Conclusions:
- HER3, EGFR, and TROP2 are highly expressed in HNSCC, indicating their potential as therapeutic targets for ADCs.
- The significant prevalence of HER2 expression in a subset of HNSCC patients warrants further investigation.
- The expression profile of these ADC targets suggests that HNSCC patients may benefit from ADC therapies.
More Related Videos
11:58Initial Evaluation of Antibody-conjugates Modified with Viral-derived Peptides for Increasing Cellular Accumulation and Improving Tumor Targeting
Published on: March 8, 2018
07:29Intramucosal Inoculation of Squamous Cell Carcinoma Cells in Mice for Tumor Immune Profiling and Treatment Response Assessment
Published on: April 22, 2019