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

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 ‘train...

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Veröffentlicht in:British journal of cancer 2021-08, Vol.125 (3), p.413-421
Hauptverfasser: Sathasivam, Hans Prakash, Kist, Ralf, Sloan, Philip, Thomson, Peter, Nugent, Michael, Alexander, John, Haider, Syed, Robinson, Max
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Sprache:eng
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Zusammenfassung: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.
ISSN:0007-0920
1532-1827
DOI:10.1038/s41416-021-01411-z