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. 2019 Nov 25;9(2):487–495. doi: 10.1002/cam4.2706

Table 3.

Correlation between NSCLC patients with brain metastases and different driver genes

  Brain metastases (n = 153) Non‐ brain metastasis (n = 399)
At first visit 108 (n, %) Follow‐up 45 (n, %) Total 153 (n, %) n, %
EGFR mutation 55 (50.9) 22 (48.9) 77 (50.3) 149 (37.3)*
18 exons 2 (1.9) 0 (0) 2 (2.5) 4 (1.0)
19 exons 20 (18.5) 10 (22.2) 30 (39.0) 56 (14.0)
20 exons 4 (3.7) 1 (2.2) 5 (6.5) 5 (1.3)
21 exons 18 (16.7) 10 (22.2) 28 (3.6) 51 (12.8)
Double point mutations 11 (10.2) 1 (2.2) 12 (1.5.6) 33 (8.3)
ALK fusion mutation 4 (3.7) 5 (11.1) 9 (5.9) 13 (3.3)*
KRAS mutation 6 (5.6) 6 (13.3) 12 (7.8) 43 (10.8)*
ROS‐1 fusion mutation 0 (0) 0 (0) 0 (0.0) 3 (0.8)
BRAF mutation 0 (0) 2 (4.4) 2 (1.3) 1 (0.3)
ERBB2 mutation 0 (0) 1 (2.2) 1 (0.7) 6 (1.5)
RET fusion mutation 7 (6.5) 0 (0) 7 (4.6) 4 (1.0)
c‐MET mutation/amplification 0 (0) 1 (2.2) 1 (1.9) 2 (0.5)
Double gene mutation 2 (1.9) 2 (4.4) 4 (2.6) 8 (2.0)
No driven gene mutation 34 (31.5) 6 (13.3) 40 (26.1) 170 (42.6)

Abbreviations: ALK, anaplastic lymphoma kinase; EGFR, epidermal growth factor receptor; NSCLC, non‐small‐cell lung cancer.

Non‐brain metastasis vs brain metastases, *P < .05.