Development and validation of a multivariable model for prediction of malignant transformation and recurrence of oral epithelial dysplasia

Author:

Mahmood HanyaORCID,Shephard Adam,Hankinson Paul,Bradburn Mike,Araujo Anna Luiza Damaceno,Santos-Silva Alan Roger,Lopes Marcio Ajudarte,Vargas Pablo Agustin,McCombe Kris D.,Craig Stephanie G.,James JacquelineORCID,Brooks Jill,Nankivell PaulORCID,Mehanna Hisham,Rajpoot NasirORCID,Khurram Syed Ali

Abstract

Abstract Background Oral epithelial dysplasia (OED) is the precursor to oral squamous cell carcinoma which is amongst the top ten cancers worldwide. Prognostic significance of conventional histological features in OED is not well established. Many additional histological abnormalities are seen in OED, but are insufficiently investigated, and have not been correlated to clinical outcomes. Methods A digital quantitative analysis of epithelial cellularity, nuclear geometry, cytoplasm staining intensity and epithelial architecture/thickness is conducted on 75 OED whole-slide images (252 regions of interest) with feature-specific comparisons between grades and against non-dysplastic/control cases. Multivariable models were developed to evaluate prediction of OED recurrence and malignant transformation. The best performing models were externally validated on unseen cases pooled from four different centres (n = 121), of which 32% progressed to cancer, with an average transformation time of 45 months. Results Grade-based differences were seen for cytoplasmic eosin, nuclear eccentricity, and circularity in basal epithelial cells of OED (p < 0.05). Nucleus circularity was associated with OED recurrence (p = 0.018) and epithelial perimeter associated with malignant transformation (p = 0.03). The developed model demonstrated superior predictive potential for malignant transformation (AUROC 0.77) and OED recurrence (AUROC 0.74) as compared with conventional WHO grading (AUROC 0.68 and 0.71, respectively). External validation supported the prognostic strength of this model. Conclusions This study supports a novel prognostic model which outperforms existing grading systems. Further studies are warranted to evaluate its significance for OED prognostication.

Funder

DH | National Institute for Health Research

Cancer Research UK

RCUK | Medical Research Council

AstraZeneca

Publisher

Springer Science and Business Media LLC

Subject

Cancer Research,Oncology

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