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. 2025 Jun 9;40(31):e184. doi: 10.3346/jkms.2025.40.e184

Table 1. Univariate analysis for chemotherapy response and progression-free survival by clinical variables.

Variables No. of cases Response to chemotherapy Progression-free survival
Responders (CR+PR) Non-responders (SD+PD) OR (95% CI) P MST, mon 95% CI Log-rank P HR (95% CI) P
Overall 266 223 (83.8) 43 (16.2) 16.6 15.4–18.5
Age, yr
< 65 121 101 (83.5) 20 (16.5) 1.00 15.4 12.4–8.2 1.00
≥ 65 145 122 (84.1) 23 (15.9) 1.05 (0.55–2.02) 0.883 18.2 15.9–21.6 0.145 0.81 (0.61–1.08) 0.146
Gender
Male 93 78 (83.9) 15 (16.1) 1.00 15.4 11.6–18.3 1.00
Female 173 145 (83.8) 28 (16.2) 0.99 (0.50–1.98) 0.991 17.4 16.0–19.6 0.099 0.78 (0.57–1.05) 0.100
Smoking status
Never 179 148 (82.7) 31 (17.3) 1.00 17.4 15.9–19.4 1.00
Ever 87 75 (86.2) 12 (13.8) 1.31 (0.63–2.69) 0.464 15.4 11.6–18.3 0.484 1.16 (0.82–1.52) 0.484
Clinical stage
19 14 (73.7) 5 (26.3) 1.00 23.6 7.59–N.D. 1.00
247 209 (84.6) 38 (15.4) 1.96 (0.67–5.77) 0.219 16.4 15.1–18.3 0.096 1.71 (0.90–3.24) 0.100
PS ECOG
0–1 86 74 (86.1) 12 (13.9) 1.00 19.4 16.6–23.6 1.00
2 180 149 (82.8) 31 (17.2) 0.78 (0.38–1.61) 0.499 15.5 12.5–17.4 0.011 1.49 (1.09–2.03) 0.011
Weight loss
No 166 136 (81.9) 30 (73.7) 1.00 16.4 13.0–18.5 1.00
Yes 19 14 (18.1) 5 (26.3) 0.62 (0.21–1.85) 0.388 15.4 6.9–29.4 0.837 1.06 (0.62–1.80) 0.837
EGFR mutation
Exon 19 deletion 148 129 (87.2) 19 (12.8) 1.00 17.4 15.5–19.4 1.00
Exon 21 L858R 111 87 (78.4) 24 (21.6) 0.53 (0.28–1.03) 0.063 15.2 10.6–18.5 1.21 (0.91–1.62) 0.193
Othersa 7 7 (100.0) 0 (0.0) 0.984 32.1 8.6–32.1 0.286 0.65 (0.21–2.05) 0.463
EGFR-TKI
1st generation 166 135 (81.3) 31 (18.7) 1.00 15.9 12.4–17.4 1.00
2nd generation 100 88 (88.0) 12 (12.0) 1.68 (0.82–3.45) 0.155 18.5 15.6–24.1 0.065 0.75 (0.56–1.02) 0.067

CR = complete response, PR = partial response, SD = stable disease, PD = progressive disease, OR = odds ratio, MST = median survival time, CI = confidence interval, HR = hazard ratio, PS = performance status, ECOG = Eastern Cooperative Oncology Group, N.D. = not determined.

aUncommon EGFR mutations; two G719A, three G719X and two S768I.