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. Author manuscript; available in PMC: 2017 Jan 1.
Published in final edited form as: Eur J Nucl Med Mol Imaging. 2016 Sep 19;44(1):17–24. doi: 10.1007/s00259-016-3520-4

Table 2.

Results of a main-effect multivariate Cox proportional hazards regression model with pre-treatment total MTV (tMTV-pre) as a continuous covariate, along with potential confounders, to predict overall survival (OS).

Parameter Estimate
(SE)
Hazard ratio
(95% CI)
P-value
Age (years): continuous 0.019 (0.010) 1.02 (1.00, 1.04) 0.053
Gender: female (vs. male) 0.091 (0.176) 1.10 (0.78, 1.55) 0.607
Baseline performance status: ambulatory, capable of light work (vs.
fully active)
0.945 (0.318) - 1 0.003
Baseline performance status * Time (months) −0.029 (0.014) - 1 0.043
Baseline clinical stage: IIIB (vs. IIB/IIIA) 0.115 (0.176) 1.12 (0.80, 1.58) 0.511
Radiation dose (Gy): continuous −0.025 (0.010) 0.98 (0.96, 0.99) 0.011
Chemotherapy regimen: Cisplatin + Etoposide (vs. Carboplatin +
Paclitaxel)
−0.027 (0.261) 0.97 (0.58, 1.62) 0.916
Chemotherapy regimen: Other (vs. Carboplatin + Paclitaxel) 0.126 (0.187) 1.13 (0.79, 1.64) 0.501
Pre-treatment SUVpeak: continuous −0.003 (0.011) 0.997 (0.98, 1.02) 0.766
Pre-treatment number of hypermetabolic lesions: continuous 0.131 (0.059) - 1 0.026
Pre-treatment number of hypermetabolic lesions * Time (months) −0.006 (0.004) - 1 0.074
tMTV-pre: continuous 2 0.033 (0.008) 1.03 (1.02, 1.05) <0.001
1

A single hazard ratio is not reported as the specified covariate is time-varying, thus implying that the hazard ratio decreases over time.

2

The reported hazard ratio corresponds to a 10mL increase in tMTV-pre.

P-value is below the statistical significance threshold of 0.017 (adjusted for multiple comparisons).

Abbreviations: SE=standard error; CI=confidence interval; tMTV-pre=pre-treatment total MTV