Table 4.
Outcomea | Unadjusted | Multivariableb | ||
---|---|---|---|---|
HR or OR (95% CI) | P | HR or OR (95% CI) | P | |
Overall survival | ||||
rsl993116 | 1.03 (0.91–1.17) | 0.64 | 0.99 (0.87–1.14) | 0.94 |
rs6013897 | 0.96 (0.83–1.12) | 0.64 | 0.94 (0.80–1.11) | 0.47 |
rsl2785878 | 1.05 (0.92–1.20) | 0.46 | 1.00 (0.86–1.16) | 0.99 |
rsl1234027 | 1.05 (0.89–1.23) | 0.57 | 1.05 (0.89–1.25) | 0.54 |
rs2282679 | 1.07 (0.92–1.24) | 0.36 | 1.06 ((Ш–1.24) | 0.42 |
Genetic risk score | 1.03 (0.97–1.08) | 0.36 | 1.01 (0.95–1.07) | 0.79 |
Time to progression | ||||
rsl993116 | 0.91 (0.80–1.04) | 0.16 | 0.89(0.77–1.02) | 0.11 |
rs6013897 | 0.92 (0.78–1.09) | 0.36 | 0.90 (0.75–1.07) | 0.23 |
rsl2785878 | 1.11 (0.97–1.28) | 0.14 | 1.09 (0.93–1.27) | 0.27 |
rsl1234027 | 1.06 (0.90–1.25) | 0.47 | 1.03 (0.87–1.23) | 0.73 |
rs2282679 | 1.06 (0.91–1.23) | 0.47 | 1.05 (0.89–1.23) | 0.56 |
Genetic risk score | 1.01 (0.95–1.07) | 0.82 | 0.99 (0.93–1.05) | 0.76 |
Tumor response | ||||
rsl993116 | 1.05 (0.82–1.35) | 0.68 | 1.04 (0.80–1.35) | 0.78 |
rs6013897 | 1.04 (0.78–1.39) | 0.78 | 1.09 (0.80–1.50) | 0.58 |
rsl2785878 | 0.95 (0.73–1.22) | 0.68 | 1.09 (0.82–1.44) | 0.56 |
rsl1234027 | 0.94 (0.69–1.28) | 0.70 | 0.98 (0.70–1.36) | 0.90 |
rs2282679 | 1.11 (0.84–1.46) | 0.45 | 1.04 (0.78–1.40) | 0.77 |
Genetic risk score | 1.01 (0.91–1.13) | 0.83 | 1.03 (0.92–1.16) | 0.57 |
25(OH)D 25-hydroxyvitamin D3, CI confidence interval, ECOG Eastern Cooperative Oncology Group, FOLFOX fluorouracil, leucovorin, oxaliplatin, GWAS genome-wide association studies, HR hazard ratio, IFL irinotecan, bolus fluorouracil, leucovorin, IROX irinotecan, oxaliplatin, OR odds ratio, SNP single-nucleotide polymorphism
Additive effect of a risk allele (i.e., associated with lower 25(OH)D levels) on patient outcome
Adjusted for age (continuous), sex (female, male), race/ethnicity (white, black, other, unknown/missing), ECOG performance status (0–1,2), number of metastatic sites (continuous), and treatment arm (IFL, FOLFOX, IROX)