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ABSTRACT: Background
A high percentage of patients with thin melanoma (TM), defined as lesions with Breslow thickness ≤1 mm, presents excellent long-term survival, however, some patients develop metastases. Existing prognostic factors cannot reliably differentiate TM patients at risk for metastases.Objective
We aimed at characterizing the clinical-pathologic and mutation profile of metastatic and not-metastatic TM in order to distinguish lesions at risk of metastases.Methods
Clinical-pathologic characteristics were recorded for the TM cases analyzed. We used a Next Generation Sequencing (NGS) multi-gene panel to characterize TM for multiple somatic mutations.Results
A statistically significant association emerged between the presence of metastases and Breslow thicknes
SUBMITTER: Richetta AG
PROVIDER: S-EPMC6114949 | biostudies-literature | 2018 Aug
REPOSITORIES: biostudies-literature