4.7 Article

Predicting the clinical outcome of oral potentially malignant disorders using transcriptomic-based molecular pathology

Journal

BRITISH JOURNAL OF CANCER
Volume 125, Issue 3, Pages 413-421

Publisher

SPRINGERNATURE
DOI: 10.1038/s41416-021-01411-z

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Funding

  1. Ministry of Health Malaysia
  2. Breast Cancer Now

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This study developed and validated a gene expression signature to characterize oral potentially malignant disorders with a high risk of malignant transformation. The signature, composed of 11 genes, was able to predict patient risk scores in the test set and stratify the risk of malignant transformation, demonstrating promising clinical utility.
Background This study was undertaken to develop and validate a gene expression signature that characterises oral potentially malignant disorders (OPMD) with a high risk of undergoing malignant transformation. Methods Patients with oral epithelial dysplasia at one hospital were selected as the 'training set' (n = 56) whilst those at another hospital were selected for the 'test set' (n = 66). RNA was extracted from formalin-fixed paraffin-embedded (FFPE) diagnostic biopsies and analysed using the NanoString nCounter platform. A targeted panel of 42 genes selected on their association with oral carcinogenesis was used to develop a prognostic gene signature. Following data normalisation, uni- and multivariable analysis, as well as prognostic modelling, were employed to develop and validate the gene signature. Results A prognostic classifier composed of 11 genes was developed using the training set. The multivariable prognostic model was used to predict patient risk scores in the test set. The prognostic gene signature was an independent predictor of malignant transformation when assessed in the test set, with the high-risk group showing worse prognosis [Hazard ratio = 12.65, p = 0.0003]. Conclusions This study demonstrates proof of principle that RNA extracted from FFPE diagnostic biopsies of OPMD, when analysed on the NanoString nCounter platform, can be used to generate a molecular classifier that stratifies the risk of malignant transformation with promising clinical utility.

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