Targeted therapy has been developed through an in-depth understanding of molecular pathways involved in the pathogenesis of melanoma. Approximately ~50% of patients with melanoma have tumors that harbor a mutation of the oncogene. Certain clinical features have been identified in -mutated melanomas (primary lesions located on the trunk, diagnosed in patients <50, visibly pigmented tumors and, at times, with ulceration or specific dermatoscopic features). While mutation testing is recommended for stage III-IV melanoma, guidelines differ in recommending mutation testing in stage II melanoma patients. To fully benefit from these treatment options and avoid delays in therapy initiation, advanced melanoma patients harboring a mutation must be identified accurately and quickly. To achieve this, clear definition and implementation of reflex testing criteria/methods in melanoma should be established so that patients with advanced melanoma can arrive to their first medical oncology appointment with a known biomarker status. Reflex testing has proven effective for a variety of cancers in selecting therapies and driving other medical decisions. We overview the pathophysiology, clinical presentation of -mutated melanoma, current guidelines, and present recommendations on mutation testing. We propose that reflex testing should be performed for every melanoma patient with stages ≥IIB.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8126223 | PMC |
http://dx.doi.org/10.3390/cancers13092282 | DOI Listing |
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