The invention is a diagnostic assay for distinguishing benign from malignant thyroid neoplasms. The assay leverages a panel of differentially expressed biomarkers for diagnosis and to predict disease staging, with utility to complement FNA biopsy of thyroid nodules.
In studies (see below) the multigene assay correctly classified 93% of tumors into the correct risk group (low-risk versus high-risk), with a sensitivity of 78.9% (true positive in high-risk tumors) and specificity of 92% (true negative in low-risk tumors). Positive and negative predictive values were 87.5% and 92%, respectively.
To commercialize the invention
Preclinical
Available under CDA
Country | Type | Number | Dated | Case |
United States Of America | Issued Patent | 7,901,888 | 03/08/2011 | 2006-092 |