DermTech, LLC, a leader in precision dermatology offering non-invasive skin genomics solutions, has published new data highlighting the effectiveness of non-invasive genomic testing in distinguishing melanoma in situ from morphologically atypical nevi when clinical and dermoscopic evaluations fall short. The study, published in the *Journal of Drugs in Dermatology* (JDD), demonstrated that non-invasive gene expression profiling (NI-GEP) helped differentiate lower-risk from higher-risk lesions, assisting clinicians in making better biopsy decisions, particularly in patients with multiple concerning moles (Peck et al., JDD, Volume 23, Issue 9, 717-723).
Gary L. Peck, MD, the lead author of the study and a recent inductee into the American Academy of Dermatology's "Titans of Dermatology," emphasized that assessing moles for melanoma remains a challenge, even for skilled dermoscopists, as some early melanomas show few morphological signs. He noted that non-invasive genomic testing offers an additional tool to aid in pigmented lesion management.
Maral K. Skelsey, MD, senior author and medical director at the Dermatologic Surgery Center of DC, where the study was conducted, added that genomic testing is essential in deciding which atypical moles to biopsy. Having used DermTech's melanoma rule-out test on over 5,000 patients, her practice has seen significant patient and business benefits from the technology.