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. 2014 Aug 25;5(5):411–416. doi: 10.1111/1759-7714.12111

Table 1.

Relationships between clinical-pathological characteristics and these three genes in patients with lung adenocarcinoma

Variable Total EML4-ALK rearrangement EGFR mutation KRAS mutation
131 n % P-value n % P-value n % P-value
Gender 0.502 0.001 0.728
 Male 74 4 5.41 26 35.14 4 5.41
 Female 57 5 8.77 37 64.91 4 7.02
Age 0.687 1.000 0.658
 ≤65 105 8 7.61 51 48.57 6 5.71
 >65 26 1 3.84 12 46.15 2 7.69
Smoking status 0.077 <0.001 0.728
 Never 74 8 10.81 46 62.16 4 5.41
 Ever 57 1 1.75 17 29.82 4 7.02
Family history 1.000 0.215 1.000
 No 112 8 7.14 51 45.54 7 6.25
 Yes 19 1 5.26 12 63.16 1 5.26
PTNM stage 0.293 0.060 0.691
 IA 29 3 10.34 13 44.83 1 3.45
 IB 32 2 6.25 15 46.88 3 9.38
 IIA 11 1 9.09 2 18.18 1 9.09
 IIB 5 1 20.00 2 40.00 1 20.00
 IIIA 38 1 2.63 21 55.26 2 5.26
 IIIB 3 1 33.33 0 0.00 0 0.00
 IV 13 0 0.00 10 76.92 0 0.00

Family history: whether the three generations of immediate family members of the patients had malignant tumor. EGFR, epidermal growth factor receptor; EML4-ALK, echinoderm microtubule-associated protein-like 4-anaplastic lymphoma kinase; KRAS, v-Ki-ras2 Kirsten rat sarcoma viral oncogene homolog; PTNM, pathological tumor node metastasis stage.