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. 2016 Jan 27;7(8):9017–9025. doi: 10.18632/oncotarget.7029

Table 2. Results of multivariate Cox regression.

Gene Adjusted HR$ 95% C.I. P value
All patients (n = 261)
EGFR 1.89 1.16 3.10 0.011
ERBB2 1.68 1.03 2.74 0.038
ERBB3 1.65 1.02 2.68 0.042
ERBB4 1.62 1.01 2.61 0.047
Wild type (n = 118)
EGFR 1.13 0.58 2.22 0.718
ERBB2 1.84 0.96 3.55 0.068
ERBB3 0.94 0.51 1.73 0.841
ERBB4 1.23 0.64 2.37 0.527
EGFR-activating mutations (n = 143)
EGFR 3.53 1.58 7.87 0.002
ERBB2 2.00 0.91 4.40 0.086
ERBB3 2.64 1.17 5.95 0.019
ERBB4 3.40 1.55 7.48 0.002
L858R (n = 70)
EGFR 2.96 1.02 8.57 0.046
ERBB2 2.86 0.91 9.03 0.074
ERBB3 3.98 1.02 15.63 0.047
ERBB4 7.22 2.23 23.36 0.001
Exon 19 deletion (n = 73)
EGFR 7.25 1.74 30.27 0.007
ERBB2 2.47 0.64 9.60 0.192
ERBB3 3.39 0.88 13.03 0.076
ERBB4 1.88 0.53 6.71 0.332
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Hazard ratio

+ EGFR-activating mutations include L858R and exon-19-deletion

The association between members of ErbB family DNA copy number abundance and overall survival was evaluated by multivariate Cox hazard regression in all 261 patients, 118 wild type patients, 70 EGFR L858R patients, 73 EGFR exon-19-deletion patients, and all 143 EGFR-activating mutation patients. Potential confounding factors such age, gender, stage, and cell type were adjusted. Hazard ratio, confidence interval, and p-value were shown.