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. 2015 Feb 28;6(7):5465–5474. doi: 10.18632/oncotarget.2925

Table 2. Relationship between driver mutation status and histologic subclassification of adenocarcinoma according to predominant type.

Total Lepidic1 Acinar2 Papillary Micropapillary Solid Mucinous3 p-value
n (%) 198 (100) 11 (5.6) 142 (71.7) 18 (9.1) 1 (0.5) 17 (8.6) 9 (4.5)
Wild-type 41 (20.7) 3 (7.3) 29 (70.7) 2 (4.9) 0 (0) 3 (7.3) 4 (9.8) 0.446 Mucinous vs. others: 0.090
Mutant type 157 (79.3) 8 (5.1) 113 (72.0) 16 (10.2) 1 (0.6) 14 (8.9) 5 (3.2)
EGFR 124 (62.6) 7 (5.6) 102 (82.3) 9 (7.3) 1 (0.8) 5 (4.0) 0 (0) < 0.001
ALK 14 (7.1) 0 (0) 6 (42.9) 2 (14.3) 0 (0) 5 (35.7) 1 (7.1) 0.012
KRAS 8 (4.0) 1 (12.5) 1 (12.5) 0 (0) 0 (0) 2 (25.0) 4 (50.0) < 0.001
PIK3CA 5 (2.5) 0 (0) 3 (60.0) 1 (20.0) 0 (0) 0 (0) 1 (20.0) 0.31
TP53 4 (2.0) 0 (0) 4 (2.8) 0 (0) 0 (0) 0 (0) 0 (0) 1
ERBB2 3 (1.5) 0 (0) 2 (66.7) 0 (0) 0 (0) 0 (0) 1 (33.3) 0.272
BRAF 2 (1.0) 0 (0) 0 (0) 2 (100) 0 (0) 0 (0) 0 (0) 0.043
ROS1 2 (1.0) 0 (0) 0 (0) 1 (50.0) 0 (0) 1 (50.0) 0 (0) 0.086
RET 2 (1.0) 0 (0) 1 (50.0) 1 (50.0) 0 (0) 0 (0) 0 (0) 0.487
NRAS 1 (0.5) 0 (0) 0 (0) 0 (0) 0 (0) 1 (100) 0 (0) 0.192
1

Two cases of minimally invasive adenocarcinoma were included in the lepidic predominant type.

2

Six cases with acinar pattern showed concurrent mutation of EGFR/PIK3CA (n = 3), EGFR/TP53 (n = 1), and ALK/TP53 (n = 2).

3

Two cases of mucinous adenocarcinoma showed concurrent mutation of KRAS/PIK3CA (n = 1) and KRAS/ERBB2 (n = 1).