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. 2020 Jun;9(3):575–586. doi: 10.21037/tlcr-19-318

Table S6. Associations between combined SNPs identified in this study and all previously published in the present study populations and survival of NSCLC in the PLCO Trial.

Number of risk genotypes1 Number2 OS3 DSS3
Death, n (%) HR (95% CI) P Death, n (%) HR (95% CI) P
3 10 7 (70.00) 1.00 5 (50.00) 1.00
4 31 20 (64.52) 0.63 (0.26–1.54) 0.312 15 (48.39) 0.69 (0.24–1.94) 0.479
5 75 36 (48.00) 1.13 (0.49–2.56) 0.778 34 (45.33) 1.45 (0.56–3.74) 0.444
6 157 100 (63.69) 1.75 (0.80–3.82) 0.162 87 (55.41) 2.01 (0.81–5.01) 0.135
7 215 119 (55.35) 1.78 (0.82–3.88) 0.146 111 (51.63) 2.26 (0.91–5.62) 0.078
8 251 176 (70.12) 2.69 (1.24–5.81) 0.012 159 (63.35) 3.27 (1.33–8.07) 0.010
9 197 153 (77.66) 2.97 (1.37–6.44) 0.006 136 (69.04) 3.43 (1.39–8.49) 0.008
10 123 96 (78.05) 3.15 (1.43–6.93) 0.004 85 (69.11) 3.66 (1.46–9.17) 0.006
11 57 44 (77.19) 3.99 (1.76–9.04) 0.001 40 (70.18) 4.90 (1.90–12.63) 0.001
12 8 8 (100.00) 5.07 (1.77–14.52) 0.003 7 (87.50) 6.01 (1.84–19.58) 0.003
13 1 0 (0.00) 0 (0.00)
Trend <0.001 <0.001
   3–7 488 282 (57.79) 1.00 252 (51.64) 1.00
   8–13 637 477 (74.88) 1.99 (1.71–2.31) <0.001 427 (67.03) 1.94 (1.66–2.28) <0.001

1, risk genotypes were ABCG1 rs225390 AA, ADAM12 rs10794069 AG+GG, DTX1 rs1732793 GA + AA, E2F3 rs3806116 GT+TT, IRAK2 rs779901 CC, VWF rs73049469 CA + AA, ITGB2 rs3788142 GA + AA, RUNX3 rs7553295 GG, AMD1 rs1279590 GG, MSRA rs73534533 CC, TNFRSF1B rs677844 TT, IKBKAP rs4978754 CC, PLCG2 rs9673682 TT and PLPP1 rs115613985 TA + AA; 2, 60 missing date were excluded, no patients with 0, 1, 2 or 14 risk genotypes; 3, adjusted for age, sex, smoking status, histology, tumor stage, chemotherapy, radiotherapy, surgery and principal components. SNP, single-nucleotide polymorphism; NSCLC, non-small cell lung cancer; PLCO, Prostate, Lung, Colorectal and Ovarian cancer screening trial; OS, overall survival; DSS, disease-specific survival; HR, hazards ratio; CI, confidence interval.