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. Author manuscript; available in PMC: 2021 May 22.
Published in final edited form as: Eur J Cancer. 2019 Aug 14;119:66–76. doi: 10.1016/j.ejca.2019.07.008

Table 5.

Clinical, pathological and genetic characterization according to tumor location in the mutational analysis subgroup

a.
Dorsal Volar Other Unknown Total
Variable (N=4) (N=23) (N=18) (N=5) (N=50)
Gender, no (%)
Female 1 (25) 12 (52.1) 10 (55.5) 1 (20) 24 (48)
Male 3 (75) 11 (47.8) 8 (44.4) 4 (80) 26 (52)
Mutational status, no (%)
BRAF 3 (75) 5 (21.7) 4 (22.2) 3 (60) 15 (30)
NRAS 1 (25) 9 (39.1) 3 (16.6) 1 (20) 14 (28)
NF1 0 4 (17.3) 2 (11.1) 1 (20) 7 (14)
KIT 0 1 (4.3) 2 (11.1) 0 3 (6)
TERT Promotor 2 (50) 2 (8.6) 7 (38.8) 2 (40) 13 (26)
No mutation 1 (25) 4 (17.3) 3 (16.6) 1 (20) 9 (18)
Histological subtype, no (%)
ALM 0 12 (52.1) 8 (44.4) 3 (60) 23 (46)
SSM 1 (25) 2 (8.6) 1 (5.5) 0 4 (8)
NM 2 (25) 4 (17.3) 1 (5.5) 1 (20) 8 (16)
U 1 (25) 5 (21.7) 8 (44.4) 1 (20) 15 (30)
b.
Tumor site Sex Mutation status

Female Male p-value BRAF WT p-value RAS WT p-value NF1 WT p-value TERT promoter WT p-value

Dorsal 1 3 0.53 3 1 0.072 1 3 0.547 0 4 0.600 2 2 0.038
Volar 12 11 5 18 9 14 4 19 2 21
other 10 8 4 14 3 2 2 16 7 11
*

Abbreviations: ALM, acral lentiginous melanoma; NM, nodular melanoma; SSM, superficial spreading melanoma; U, unknown.