Skip to main content
. 2019 May 20;22(5):299–305. [Article in Chinese] doi: 10.3779/j.issn.1009-3419.2019.05.06

2.

150例患者EGFR少见突变患者的临床病理特征

Clinical and pathological characteristic in 150 patients with EGFR rare mutations

Variable All patients 18 G719X 21 L861Q Other single mutations Complex mutations χ2 P
Gender
  Male 53 (35.3%) 16 (34.8%) 14 (31.1%) 6 (42.9%) 17 (37.8%) 0.822 0.84
  Female 97 (64.7%) 30 (65.2%) 31 (68.9%) 8 (57.1%) 28 (62.2%)
Age (yr)
  >60 85 (56.7%) 22 (47.8%) 29 (64.4%) 8 (57.1%) 26 (57.8%) 2.597 0.46
  ≤60 65 (43.3%) 24 (52.2%) 16 (35.6%) 6 (42.9%) 19 (42.2%)
Stage
  Ⅰa-Ⅲa 14 (9.38%) 6 (13.0%) 1 (2.2%) 2 (14.3%) 5 (11.1%) 10.179 0.10
  Ⅲb-Ⅳ 81 (54.0%) 28 (60.9%) 22 (48.9%) 5 (35.7%) 26 (57.8%)
  NA 55 (36.7%) 12 (26.1%) 22 (48.9%) 7 (50.0%) 14 (31.1%)
Pathology
  Adenocarcinoma 147 (98%) 45 (97.8%) 44 (97.8%) 14 (100.0%) 44 (97.8%) 0.769 1.00
  Non-adenocarcinoma 3 (2.0%) 1 (2.2%) 1 (2.2%) 0 (0.0%) 1 (2.2%)
Smoking history
  No 94 (62.7%) 27 (58.7%) 31 (68.9%) 7 (50.0%) 29 (64.4%) 3.037 0.81
  Yes 24 (16.0%) 9 (19.6%) 6 (13.3%) 2 (14.3%) 7 (15.6%)
  NA 32 (21.3%) 10 (21.7%) 8 (17.8%) 5 9 (20.0%)