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Adult melanoma has undergone extensive genomic analysis, but pediatric melanoma has not received such scrutiny. Although rare (incidence rates of malignant melanoma per 1 million children: 1.8 in age ≤14; 11.7 in age 15–19) pediatric melanoma is highly lethal. Lu and colleagues used whole-genome sequencing, RNA sequencing, and molecular inversion probe analysis to identify copy number variations (CNVs) in 23 pediatric melanomas (13 conventional [CM], 5 congenital nevi-associated [CMN], 5 spitzoid [SM]) in patients 20 and younger. Like adult melanomas, the pediatric CMs had a tremendous mutational load (14.36 mutations per Mb). Over 80% of these tumors had changes consistent with UVB-signature C→T transition mutations.
Thirteen of 15 CMs had …