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. 2020 Sep 3;11(10):2987–2992. doi: 10.1111/1759-7714.13628

Table 2.

Association between EGF+61 genotype and alleles from TKI‐treated NSCLC patients harboring EGFR‐sensitizing mutations (n = 111) and TKI treatment response

PR SD DP
Response to TKI treatment n % n % n % P‐value
Genotype (codominant model)
AA 23 29.5% 10 55.6% 2 13.3% 0.046
AG 42 53.8% 4 22.2% 9 60.0%
GG 13 16.7% 4 22.2% 4 26.7%
Genotype (recessive model)
AA 23 29.5% 10 55.6% 2 13.3% 0.023
AG + GG 55 70.5% 8 44.4% 13 86.7%
Genotype (dominant model)
AA + AG 65 83.3% 14 77.8% 11 73.3% 0.601
GG 13 16.7% 4 22.2% 4 26.7%
Allele frequency
A 56.4% 66.7% 43.3% 0.163
G 43.6% 33.3% 56.7%

Bold P‐values indicate P ≤ 0.05 from univariate analysis (χ2 test).

DP, disease progression; PR, partial response; SD, stable disease.