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. 2018 Jun;7(3):416–427. doi: 10.21037/tlcr.2018.05.01

Table 2. Genomic regions with prognostic effect of copy number aberrations (CNA).

Region ID Chr cytoBands Mb CNA frequency Disease-free survival Overall survival Lung-cancer specific survival Genes
Loss Gain HR for loss* (95% CI) HR for gain** (95% CI) P Q HR for loss* (95% CI) HR for gain** (95% CI) P Q HR for loss* (95% CI) HR for gain** (95% CI) P Q
142 7 p12.3–p11.2 8.0E+0 0.7% 17% 0.51 (0.31–0.82) 2.0 (1.2–3.2) 0.005 0.142
185 8 p11.1–q11.1 4.0E+0 7.3% 17.4% 2.0 (1.2–3.1) 0.51 (0.32–0.82) 0.005 0.130
211 9 p21.3 3.0E−1 34.8% 3.4% 1.7 (1.3–2.3) 0.57 (0.44–0.76) <0.001 0.020 1.8 (1.4–2.5) 0.55 (0.41–0.74) <0.001 0.029 1.8 (1.4–2.4) 0.55 (0.41–0.74) <0.001 0.019
212 9 p21.3 6.0E−1 35.9% 3.3% 1.6 (1.2–2.0) 0.64 (0.49–0.84) 0.001 0.076 1.7 (1.3–2.2) 0.59 (0.44–0.79) <0.001 0.044 1.6 (1.2–2.1) 0.62 (0.47–0.83) 0.001 0.062
213 9 p21.3 6.0E−2 38.7% 3.2% 1.5 (1.2–1.9) 0.67 (0.53–0.86) 0.001 0.076 1.5 (1.2–2.0) 0.66 (0.51–0.86) 0.002 0.079 1.5 (1.2–2.0) 0.65 (0.50–0.85) 0.001 0.062
214 9 p21.3 3.0E−1 40.2% 3.0% 1.5 (1.2–1.9) 0.66 (0.53–0.81) <0.001 0.020 1.5 (1.2–1.9) 0.67 (0.54–0.84) <0.001 0.049 1.6 (1.2–2.0) 0.64 (0.51–0.80) <0.001 0.021 CDKN2A, CDKN2B
215 9 p21.3 2.0E+0 36.3% 3.3% 1.6 (1.2–2.1) 0.62 (0.48–0.81) <0.001 0.034 1.7 (1.3–2.2) 0.59 (0.45–0.79) <0.001 0.044 1.7 (1.3–2.2) 0.61 (0.46–0.80) <0.001 0.029
217 9 p21.3 9.0E−3 35.0% 3.9% 1.7 (1.3–2.2) 0.60 (0.46–0.79) <0.001 0.026 1.5 (1.2–2.1) 0.65 (0.48–0.87) 0.004 0.084 1.7 (1.3–2.3) 0.58 (0.44–0.78) <0.001 0.026
218 9 p21.3 5.0E−1 32.8% 4.5% 1.6 (1.2–2.2) 0.61 (0.45–0.82) 0.001 0.076 1.7 (1.2–2.3) 0.60 (0.43–0.83) 0.002 0.079 1.7 (1.2–2.4) 0.59 (0.42–0.82) 0.002 0.064
219 9 p21.3–2 2.0E+0 30.5% 4.6% 1.8 (1.2–2.6) 0.57 (0.39–0.82) 0.003 0.106 1.8 (1.2–2.7) 0.56 (0.37–0.83) 0.004 0.084 1.9 (1.2–2.8) 0.54 (0.36–0.80) 0.002 0.085
220 9 p21.2 2.0E−2 30.1% 4.8% 1.6 (1.2–2.1) 0.64 (0.47–0.86) 0.004 0.11
222 9 p21.1 2.0E+0 27.8% 5.2% 1.9 (1.2–2.8) 0.54 (0.36–0.81) 0.003 0.084
223 9 p21.1 7.0E−1 26.0% 6.4% 1.8 (1.2–2.8) 0.54 (0.36–0.82) 0.003 0.084
312 14 q23.1 1.0E−1 8.5% 8.9% 2.2 (1.3–3.6) 0.46 (0.28–0.76) 0.002 0.079
366 18 q12.1 1.0E+0 10.8% 8.6% 1.9 (1.2–3.1) 0.52 (0.32–0.82) 0.005 0.105
367 18 q12.1 6.0E−1 10.9% 7.1% 2.0 (1.2–3.3) 0.49 (0.30–0.80) 0.005 0.092
368 18 q12.1 1.0E−3 12.1% 6.6% 1.6 (1.2–2.3) 0.61 (0.44–0.85) 0.004 0.119 1.7 (1.2–2.5) 0.58 (0.41–0.82) 0.002 0.079 1.7 (1.2–2.4) 0.59 (0.42–0.85) 0.004 0.11
376 19 p13.3 1.0E+0 10.7% 0.4% 2.4 (1.3–4.3) 0.42 (0.23–0.77) 0.005 0.142 FSTL3, STK11
378 19 p13.3–2 8.0E+0 9.2% 0.3% 2.6 (1.4–4.8) 0.38 (0.21–0.72) 0.003 0.106 2.9 (1.5–5.6) 0.34 (0.18–0.66) 0.001 0.078 3.4 (1.7–6.6) 0.29 (0.15–0.58) <0.001 0.029 MLLT1, SH3GL1, TCF3, VAV1
379 19 p13.2 3.0E−3 10.3% 0.9% 2.2 (1.3–3.8) 0.45 (0.26–0.76) 0.003 0.106 2.3 (1.3–4.2) 0.43 (0.24–0.77) 0.004 0.092 2.6 (1.4–4.6) 0.39 (0.22–0.69) 0.001 0.062
380 19 p13.2–p12 1.0E+1 8.0% 2.2% 2.7 (1.4–5.1) 0.38 (0.20–0.73) 0.004 0.084 LYL1, RAB8A, ELL, CDKN2D
383 19 p12–p11 4.0E+0 8.0% 2.5% 2.4 (1.4–4.2) 0.42 (0.24–0.74) 0.003 0.106 2.7 (1.5–5.0) 0.36 (0.2–0.66) <0.001 0.066 2.5 (1.3–4.5) 0.41 (0.22–0.75) 0.004 0.11

The univariate hazard ratio (HR) for loss shows the relative risk of a patient with a 2-fold lower CN, for example one copy as compared to two copies. The HR for gain shows the relative risk of a patient with a 2-fold higher CN, for example four copies as compared to two copies. Of note, HR for gain is 1/HR for loss. CI, confidence interval; Chr, chromosome. *, hazard ratio for a 2-fold lower copy number; **, hazard ratio for a 2-fold higher copy number.