Skip to main content
. 2013 Aug 7;30(3):679. doi: 10.1007/s12032-013-0679-4

Table 3.

Logistic regression model of clinical features for predicting time to tumour progression (TTP)

Parameter n TTP (months) Median Min. Max. Univariate analysis*
p value
BMI, kg/m2 0.004
 <25 21 11.70 5.68 19.02
 ≥25 33 6.00 1.38 17.74
CEA median (ng/ml) 0.566
 <28 34 9.49 1.38 18.60
 ≥28 20 7.26 3.68 19.02
Age (years) 0.264
 <60 27 9.49 3.25 19.02
 ≥60 27 7.00 1.38 17.74
Primary tumour 0.618
 Intact 9 10.28 1.38 18.60
 Non-intact 45 7.52 2.00 19.02
K-ras mutation status 0.683
 Wild type 25 9.49 1.38 17.74
 Mutated 29 7.00 3.25 19.02
Chemotherapy 0.683
 Irinotecan-based 35 8.71 3.25 19.02
 Oxaliplatin-based 19 7.00 1.38 18.60
No. of disease sites 0.032
 <2 33 10.28 2.00 19.02
 ≥2 21 5.72 1.38 17.74

In multivariate analysis, the only independent prognostic factor for TTP was BMI (p = 0.01; HR 4.37; 95 % CI 1.34–14.78) for patients with mCRC treated with combination chemotherapy and bevacizumab

* Mann–Whitney U test