Thymoma and thymic carcinomas are a rare and poorly understood group of malignancies. Despite the growing number of biomarkers that are used for diagnosing and treating carcinomas in general, cancers of the thymus are still diagnosed, stratified and treated by a costly combination of histology, surgery and radiological procedures. The lack of qualified biomarkers associated with thymomas and thymic carcinomas has also hampered the development of targeted therapies.
Researchers at NCI discovered a missense mutation in the general transcription factor Iii (GTF2I) at high frequency in non-aggressive forms of thymoma, as well as a series of common oncogene mutations in aggressive thymic carcinomas. The technology provides a method for determining the prognosis of thymic cancer and informing clinical decisions regarding treatment regiments by a simple PCR based test.
- A diagnostic test kit for the diagnosis and stratification of thymic cancers .
- A simple and inexpensive test that will inform clinical treatment decisions
- The PCR based method is cheaper, more sensitive and more objective than currently available histological classification and stratification
- Prevents the need for extensive radiological tests in non-agressive thymomas
- Provides the basis for developing new targeted therapies, or to identify currently available therapies that can be used to treat thymic cancers.
Petrini I, et al. [PMID 24974848]
- U.S. Patent Filed: U.S. Patent Application Number 14/676,987, Filed 02 Apr 2015