Skip to main content
. 2017 Jul 19;14(3):3601–3605. doi: 10.3892/ol.2017.6608

Table III.

Association of BRAF gene mutation with clinicopathological features.

Characteristics BRAF wide-type (n=752) n (%) BRAF V600E mut (n=147) n (%) BRAF 594 or 596 mut (n=13) n (%) P-valuea P-valueb P-valuec
Sex 0.091 0.109 0.303
  Male 397 (52.8) 67 (45.6) 4 (30.8)
  Female 355 (47.2) 80 (54.4) 9 (69.2)
Age (years) <0.001 <0.001 0.017
  Median 55 49 58
  Range 7–92 7–84 25–75
Subtype <0.001 <0.001 <0.001
  Acral 395 (52.5) 58 (39.5) 3 (23.1)
  Mucosal 208 (27.7) 14 (9.5) 7 (53.8)
  Non-acral cutaneous 149 (19.8) 75 (51) 3 (23.1)
Clinical stage <0.001 <0.001 0.801
  I 8 (1.1) 2 (1.4) 0 (0)
  II 439 (58.4) 39 (26.5) 5 (38.5)
  III 165 (21.9) 29 (19.7) 2 (15.4)
  IV 140 (18.6) 77 (52.4) 6 (46.2)
Ulceration 0.034 0.030 0.043
  Yes 426 (56.6) 90 (66.7) 5 (38.5)
  No 326 (43.4) 45 (33.3) 8 (61.5)
Thickness (mm) 0.017 0.008 0.124
  ≤1.0 71 (9.4) 12 (8.2) 0 (0)
  1.1–2.0 86 (11.4) 9 (6.1) 3 (23.1)
  2.1–4.0 196 (26.1) 26 (17.7) 2 (15.4)
  >4.0 399 (53.1) 100 (6.8) 8 (61.5)
a

Comparison of the three groups (BRAF wild-type versus BRAF V600E mut versus BRAF 594 or 596 mut).

b

Comparison of BRAF wild-type versus BRAF V600E mut.

c

Comparison of BRAF V600E mut versus BRAF 594 or 596 mut.