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. 2017 Jun 15;117(3):358–366. doi: 10.1038/bjc.2017.170

Table 1. Clinicopathological features of tumour specimens in relation to KRAS, NRAS and BRAF gene mutation status.

  KRAS mut n (%) NRAS mut n (%) BRAF mut n (%) RAS/BRAF WT n (%) Total n (%)
Sex
F 52 (48.1) 6 (5.6) 10 (9.3)a 40 (37.0) 108 (45.0)
M 61 (46.2) 8 (6.1) 2 (1.5) 61 (46.2) 132 (55.0)
Sub total 113 (47.1) 14 (5.8) 12 (5.0) 101 (42.1) 240 (100)
Age (years)
Median 64 68 65,5 63,5
Range 34–84 40–87 51–73 22–92
Sub total 101 (47.2) 13 (6.1) 10 (4.7) 90 (42.0) 214 (100)
G
1–2 57 (48.7) 5 (4.3) 1 (0.9) 54 (27.3) 117 (71.8)
3–4 21 (45.6) 4 (8.7) 5 (10.9)a 16 (34.8) 46 (28.2)
Sub total 78 (47.8) 9 (5.5) 6 (3.7) 70 (42.9) 163 (100)
pT
1–2 5 (55.5) 1 (11.1) 0 (0) 3 (0) 9 (5.5)
3–4 73 (47.4) 8 (5.2) 6 (3.4) 67 (43.5) 154 (94.5)
Sub total 78 (47.8) 9 (5.5) 6 (3.7) 70 (42.9) 163 (100)
pN
0 19 (46.3) 3 (7.3) 2 (4.9) 17 (41.5) 41 (25.6)
1 36 (56.3) 3 (4.7) 0 (0) 25 (39.1) 64 (40.0)
2 21 (38.2) 2 (3.6) 4 (7.3) 28 (50.9) 55 (34.4)
Sub total 76 (47.5) 8 (5.0) 6 (3.8) 70 (43.7) 160 (100)
Vascular and/or perineural invasion
Yes 52 (44.8) 6 (5.2) 4 (3.4) 54 (41.7) 116 (78.4)
No 17 (53.1) 2 (6.3) 1 (3.1) 12 (37.5) 32 (21.6)

Abbreviations: mut=mutated; WT=wild-type; F=female; M=male.

a

BRAF mutations are significantly more prevalent in female patients (F) and G3-G4 tumours rather than in males (M) and G1-G2 tumours (P=0.013).