DermTech, Inc. announced the publication of “Real-world performance and utility of a noninvasive gene expression assay to evaluate melanoma risk in pigmented lesions,” by Dr. Laura Ferris of the University of Pittsburgh, et al, in Melanoma Research.
“We knew we had a very well validated non-invasive melanoma rule-out test with a negative predictive value of over 99%. Preliminary utility data from an earlier reader study showed that dermatologists biopsy less often while detecting more early-stage melanomas when using DermTech’s pigmented lesion assay. This study now confirms similar exceptional utility in the real-world. The PLA effectively helps clinicians manage pigmented lesions, by avoiding unnecessary biopsies while identifying early melanoma. Consistent with the high NPV of the test, there were no missed melanomas in the follow up period,” said Dr. Laura Ferris.
About DermTech
DermTech is the global leader in molecular dermatology, bringing precision medicine to the diagnosis and treatment of skin disease. We market and develop products that facilitate the early detection of skin cancers, assess inflammatory diseases, and customize drug treatments. DermTech analyzes skin biopsy samples collected non-invasively using an adhesive patch rather than a scalpel. Our mission is to transform dermatology by delivering highly accurate and objective information to the clinician to improve care and reduce costs and to pharma partners to support the development of targeted therapeutics. For additional information visit dermtech.com.
View source version on businesswire.com: https://www.businesswire.com/news/home/20180718005755/en/
Source: DermTech, Inc.