AMLo Biosciences’ Post

Calling all US-based Dermatology Physician Associates heading off to the #SDPA #derm_pa Conference, this week. Take a look at our recent opinion piece from Karoline Dempsey, Board-Certified Physician Assistant and Diplomate of Dermatology, on using #AMBLor #melanoma prognostic test in clinical practice. The immunohistochemistry-based assay AMBLor identifies two biomarker proteins in the initial skin sample from early-stage melanoma patients and accurately identifies those at low risk of progression. “We know what to do with very aggressive, deep melanomas, and we know what to do with the very thin melanomas,” PA Dempsey says. It’s all the cases in between that make it so difficult to identify the patients at highest risk for aggressive cancer. That’s why novel risk assessment tools are so important for healthcare providers.” With this additional prognostic information from AMBLor, the oncology team can personalise the treatment and follow-up plan. AMBLor® testing service is provided by Avero Diagnostics as a physician-ordered, laboratory-developed test (LDT). The AMBLor test meets the U.S. Food and Drug Administration (FDA) definition and requirements for LDTs, but it has not been reviewed by the FDA. AMBLor has received its UKCA mark in the UK. #dermPAsforDermPAs #dermatology #dermconference #skincancer #oncology #dermatopathology #histopathology #biomarkers

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