Assessing Oral Epithelial Dysplasia Risk for Transformation to Cancer: Comparison Between Histologic Grading Systems Versus S100A7 Immunohistochemical Signature-based Grading

Author:

Darling Mark Roger1ORCID,Hwang Jason T.K.2,Dickson Benjamin J.3,Cutz Jean-Claude4,Salama Samih4,McCord Christina5,Pritzker Kenneth P.H.672,Mock David8,Thompson Lester D.R.9

Affiliation:

1. Schulich School of Medicine and Dentistry, The University of Western Ontario

2. Proteocyte Diagnostics Inc.

3. Sixsense Strategy Group

4. Department of Pathology and Molecular Medicine, McMaster University, Hamilton

5. Department of Pathology and Laboratory Medicine, Schulich School of Medicine and Dentistry, The University of Western Ontario, London

6. Departments of Laboratory Medicine and Pathobiology, Surgery Temerty Faculty of Medicine, University of Toronto

7. Pathology and Laboratory Medicine, Mount Sinai Hospital

8. Department of Laboratory Medicine & Pathobiology, Faculty of Dentistry, University of Toronto, Toronto, ON, Canada

9. Head and Neck Pathology Consultations, Woodland Hills, CA, USA

Abstract

While a 3-tier oral epithelial dysplasia grading system has been utilized for decades, it is widely recognized as a suboptimal risk indicator for transformation to cancer. A 2-tier grading system has been proposed, although not yet validated. In this study, the 3-tier and 2-tier dysplasia grading systems, and an S100A7 immunohistochemical signature-based grading system were compared to assess prediction of risk of transformation to oral cancer. Formalin-fixed, paraffin-embedded biopsy specimens with known clinical outcomes were obtained retrospectively from a cohort of 48 patients. Hematoxylin and eosin-stained slides were used for the 2- and 3-tier dysplasia grading, while S100A7 for biomarker signature-based assessment was based on immunohistochemistry. Inter-observer variability was determined using Cohen’s kappa (K) statistic with Cox regression disease free survival analysis used to determine if any of the methods were a predictor of transformation to oral squamous cell carcinoma. Both the 2- and 3-tier dysplasia grading systems ranged from slight to substantial inter-observer agreement (Kw between 0.093 to 0.624), with neither system a good predictor of transformation to cancer (at least P=0.231; (P>>>0.05). In contrast, the S100A7 immunohistochemical signature-based grading system showed almost perfect inter-observer agreement (Kw=0.892) and was a good indicator of transformation to cancer (P=0.047 and 0.030). The inherent grading challenges with oral epithelial dysplasia grading systems and the lack of meaningful prediction of transformation to carcinoma highlights the significant need for a more objective, quantitative, and reproducible risk assessment tool such as the S100A7 immunohistochemical signature-based system.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Medical Laboratory Technology,Histology,Pathology and Forensic Medicine

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