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. 2019 Mar 1;9:3209. doi: 10.1038/s41598-019-39965-x

Table 2.

Multivariate analysis of the association between clinicopathological characteristics and ancestry background and EGFR and KRAS mutations.

Variables Parameters Total (n) OR 95% CI p-value
EGFR Gender Male 224 1 Ref. Ref.
Female 196 1.67 0.98–2.85 0.058
Tobacco Never 126 5.11 2.71–9.62 <0.0001
Current smoker 166 0.59 0.28–1.24 0.16
Former smoker 128 1 Ref. Ref.
ASN Ancestry Low 140 1 Ref. Ref.
Intermediate 138 1.05 0.54–2.04 0.88
High 142 2.01 1.09–3.71 0.03
PS ECOG 0 44 3.94 1.47–10.57 0.006
1 222 1.67 0.79–3.53 0.18
2 67 1.2 0.46–3.13 0.72
3 or 4 84 1 Ref. Ref
KRAS Tobacco Never 126 1 Ref. Ref.
Current smoker 166 3.42 1.67–7.00 0.001
Former smoker 128 3.74 1.79–7.81 <0.0001
ASN Ancestry Low 140 1.93 1.06–3.52 0.03
Intermediate 138 1.31 0.69–2.46 0.41
High 142 1 Ref. Ref.

n, number of patients; OR, odds ratio; 95% CI, 95% confidence interval; p-value: significance of Wald test.; ASN, Asian race; Ref., reference group; PS ECOG, performance status ECOG (Eastern Cooperative Oncology Group). Significant associations are indicated in bold.