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. 2018 Feb 13;118(6):785–792. doi: 10.1038/bjc.2017.489

Table 2. Univariate and multivariate analysis of the vemurafenib subgroup.

  Univariate analysis
Multivariate analysis
Variable Hazard ratio 95% CI P Hazard ratio 95% CI P
ECOG (0 (n=29) vs >0 (n=38)) 1.007 0.505–2.006 0.985
LDH (⩽ 250 (n=26) v.>250 U/l (n=41)) 1.514 0.805–2.849 0.199 1.698 0.959–3.008 0.070
Brain metastases (no (n=26) vs yes (n=41)) 1.194 0.637–2.24 0.580
Period BRAFi RT (⩽58 days (n=37) vs>58 days (n=30)) 1.155 0.668–1.999 0.606
Toxicity (no (n=33) vs any (n=34)) 1.656 0.622–4.407 0.312 1.455 0.635–3.334 0.376
Drugs (only BRAFi (n=30) vs drug prior to BRAFi (n=37)) 1.746 0.991–3.077 0.054 1.654 0.955–2.866 0.073
Vemurafenib (concomitant (n=36) vs interrupted (n=31)) 0.683 0.309–1.512 0.347 0.507 0.293–0.877 0.015

Abbreviations: BRAFi=BRAF inhibitor; CI=confidence interval; ECOG=Eastern Cooperative Oncology Group; LDH=lactate dehydrogenase.

Variables associated with a P-value <0.35 in univariate analyses were considered for inclusion in multivariate analyses. P-values <0.05 were considered to be statistically significant and were marked in bold.