Table 1. Treatment effect for progression-free and overall survival according to the level of expression for each biomarker.
Treatment effect (C
vs
CB+CBM)a |
|||||||||
---|---|---|---|---|---|---|---|---|---|
|
0, 1+ | 2+ | 3+ |
Interaction Pb |
|||||
Biomarker | n | HR (95% CI) | n | HR (95% CI) | n | HR (95% CI) | Pc | Pd | Pe |
Progression-free survival | |||||||||
VEGF-A | 64 | 0.44 (0.26–0.76) | 141 | 0.64 (0.44–0.93) | 62 | 0.84 (0.48–1.48) | 0.15 | 0.22 | 0.30 |
VEGF-B | 105 | 0.47 (0.30–0.73) | 91 | 0.80 (0.51–1.24) | 71 | 0.80 (0.46–1.38) | 0.11 | 0.16 | 0.69 |
VEGF-C | 113 | 0.55 (0.37–0.83) | 83 | 0.60 (0.36–1.00) | 70 | 0.72 (0.43–1.21) | 0.40 | 0.78 | 0.19 |
VEGF-D | 32 | 0.22 (0.08–0.55) | 117 | 0.67 (0.45–1.00) | 110 | 0.77 (0.50–1.17) | 0.02 | 0.04 | 0.04 |
VEGFR-1 | 85 | 0.42 (0.26–0.68) | 89 | 0.95 (0.57–1.57) | 87 | 0.65 (0.41–1.04) | 0.21 | 0.49 | 0.55 |
VEGFR-2 | 101 | 0.51 (0.33–0.79) | 102 | 0.60 (0.37–0.96) | 62 | 0.84 (0.50–1.44) | 0.19 | 0.35 | 0.95 |
Overall survival | |||||||||
VEGF-A | 64 | 1.00 (0.53–1.86) | 141 | 0.75 (0.49–1.14) | 62 | 1.18 (0.63–2.21) | 0.74 | 0.98 | 0.86 |
VEGF-B | 105 | 0.55 (0.33–0.91) | 91 | 1.12 (0.67–1.85) | 71 | 1.30 (0.71–2.38) | 0.02 | 0.004 | 0.46 |
VEGF-C | 113 | 0.56 (0.36–0.89) | 83 | 1.18 (0.65–2.16) | 70 | 1.40 (0.75–2.58) | 0.02 | 0.05 | 0.36 |
VEGF-D | 32 | 0.35 (0.13–0.90) | 117 | 0.82 (0.52–1.30) | 110 | 1.28 (0.79–2.09) | 0.01 | 0.02 | 0.24 |
VEGFR-1 | 85 | 0.41 (0.24–0.69) | 89 | 1.37 (0.78–2.40) | 87 | 1.53 (0.86–2.73) | 0.001 | 0.002 | 0.06 |
VEGFR-2 | 101 | 0.48 (0.30–0.79) | 102 | 1.12 (0.66–1.90) | 62 | 1.67 (0.87–3.21) | 0.003 | 0.004 | 0.93 |
Abbreviations: C=apecitabine; CB=capecitabine and bevacizumab; CBM=capecitabine, bevacizumab, and mitomycin; CI=confidence interval; HR=hazard ratio; VEGF=vascular endothelial growth factor; VEGFR=vascular endothelial growth factor receptor.
Scores for treatment effect (0, 1+ 2+ 3+) are based on the staining intensity of the antibody in tumour samples.
P indicates the level of significance for the interaction between treatment (C vs CB+CBM) and the biomarker.
Analysis unadjusted.
Analysis adjusted for baseline clinicopathological characteristics.
Analysis adjusted for other biomarkers.