Skip to main content
. 2020 Aug 20;20(5):129. doi: 10.3892/ol.2020.11990

Table IV.

Comparison of clinicopathologic characteristics according to mutation profiles identified by Oncomine focus assay.

Characteristics No alterations (n=28) Other alterationsa (n=14) PIK3CA alterations (n=8) P-value
Male 19 (68%) 9 (64%) 8 (100%) 0.152
Age, years (range) 62 (39–84) 64 (53–91) 77 (52–89) 0.156
Differentiation 0.675
  Moderate 14 (50%) 6 (43%) 5 (63%)
  Poor 14 (50%) 8 (57%) 3 (37%)
TNM T stage 0.044
  2 1 (4%) 3 (21%) 0 (0%)
  3 11 (39%) 1 (7%) 1 (12%)
  4a 16 (57%) 10 (72%) 7 (88%)
TNM N stage 0.892
  0 5 (18%) 3 (21%) 2 (25%)
  1 6 (21%) 3 (21%) 2 (25%)
  2 5 (18%) 5 (37%) 2 (25%)
  3a/ 10 (36%) 2 (14%) 2 (25%)
  3b 2 (7%) 1 (7%) 0 (0%)
TNM M stage 0.702
  0 27 (96%) 13 (93%) 8 (100%)
  1 1 (4%) 1 (7%) 0 (0%)
Lauren's classification 0.028b
0.076c
  Diffuse 10 (36%) 5 (36%) 0 (0%)
  Intestinal 16 (57%) 6 (43%) 8 (100%)
  Mixed 2 (7%) 3 (21%) 0 (0%)
a

Alternations other than PIK3CA (single nucleotide variant, small insertion, duplication, deletion and amplification) identified by the Oncomine focus assay in the present study.

b

The distribution of Lauren's classification in AGC with PIK3CA alterations vs. AGC with alterations other than PIK3CA.

c

GC with PIK3CA alterations vs. AGC with no alterations. PIK3CA, PI3K catalytic subunit α; Lauren's classification (4); TNM, Tumor-Node-Metastasis (4).