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. 2020 May 6;12(5):1171. doi: 10.3390/cancers12051171

Table 4.

Clinical and molecular characteristics of BRAF mutant cancers with APC mutation.

APC p-Value 1
Characteristic n Truncating Mutation Missense Mutation Wild-Type Truncating vs. Missense Truncating vs. Wild-Type Missense vs. Wild-Type
Mean Age Years 273 60.8 72.4 70.6 2.03 × 10−5 9.3 × 10−6 0.34
Sex Male 87 (31.8%) 18 (32%) 6 (24%) 63 (33%) 0.48 0.86 0.36
Female 187 (68.2%) 39 (68%) 19 (76%) 129 (67%)
Tumour Side Left 42 (16.6%) 13 (25%) 1 (4%) 28 (16%) 0.02 0.16 0.08
Right 211 (83.4%) 40 (75%) 23 (86%) 148 (84%)
Stage I 32 (12.9%) 3 (6%) 2 (9%) 27 (16%) 0.01 0.002 0.32
II 93 (37.7%) 14 (27%) 12 (55%) 67 (39%)
III 59 (23.9%) 10 (19%) 6 (27%) 43 (25%)
IV 63 (25.5%) 25 (48%) 2 (9%) 36 (21%)
CIMP High 128 (81.0%) 20 (83%) 18 (95%) 90 (78%) 0.23 0.57 0.05
Negative 30 (19.0%) 4 (17%) 1 (5%) 25 (22%)
MSI MSI 136 (54.8%) 22 (42%) 21 (91%) 93 (54%) 5.3 × 10−5 0.14 0.0002
MSS 112 (45.2%) 30 (58%) 2 (9%) 80 (46%)

1p-values were obtained using the likelihood–ratio test for categorical variables, and the Student’s t-test for continuous variables. All statistical analyses were two-tailed. Bold text indicates significance at p < 0.05