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. 2017 Jul 20;8(65):108522–108533. doi: 10.18632/oncotarget.19411

Table 1. The detailed characteristics between the NSCLC patients with/without BIM polymorphism (n = 245).

Basic clinicopathologic factors Total
(n = 245)
BIM deletion
(n = 43)
BIM wild-type
(n = 202)
p value
Age, mean ± SD 58 ± 10 58 ± 10 58 ± 10 0.973
Age 0.862
 < 63 178 (73%) 32 (74%) 146 (72%)
 ≥ 63 67 (27%) 13 (30%) 54 (27%)
Sex 0.127
 Male 74 (30%) 10 (24%) 64 (32%)
 Female 171 (70%) 33 (76%) 138 (68%)
Smoking history 0.289
 Never 184 (75%) 31 (72%) 153 (76%)
 Ever 61 (25%) 12 (28%) 49 (24%)
ECOG PS 0.473
 0–1 227 (93%) 41 (95%) 186 (92%)
 2–4 18 (7%) 2 (5%) 16 (8%)
Histology 0.985
 Adenocarcinoma 240 (98%) 43 (100%) 197 (97%)
 Squamous 5 (2%) 0 5 (3%)
Stage
 IIIB 12 (5%) 0 12 (6%) 0.063
 IV 168 (68%) 27 (63%) 147 (70%)
 Postoperative recurrence 65 (27%) 16 (37%) 49 (24%)
No. of metastasis 0.859
 1–2 189 (77%) 34 (79%) 155 (77%)
 ≥ 3 56 (23%) 9 (21%) 47 (23%)
EGFR mutation 0.327
 Exon 19 deletion 142 (58%) 28 (65%) 114 (56%)
 L858R mutation 90 (37%) 13 (30%) 77 (38%)
 Others* 13 (5%) 2 (5%) 11 (6%)
EGFR TKIs 0.272
 Gefitinib 147 (60%) 28 (65%) 119 (59%)
 Erlotinib 98 (40%) 15 (35%) 83 (40%)
Line of EGFR TKIs 0.621
 First 86 (35%) 16 (37%) 70 (35%)
 Second 97 (40%) 18 (42%) 79 (39%)
 Third line or later 62 (25%) 9 (21%) 53 (26%)
TKIs treatment response 191 (78%) 7 (16%) 184 (91%) 0.001

Note: *was refered as others mutation, included exon 18 point mutation, and complex mutation contained the deletion and missense mutation.