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Table 3 Univariate and multivariate cox proportional hazards regression for PFS

From: Evaluation of therapeutic effect and prognostic value of 18F-FDG PET/CT in different treatment nodes of DLBCL patients

 

Variables

Univariate analysis

Multivariate analysis

p value

HR

95% CI

p value

HR

95% CI

Clinical characteristics

COO subtypes

Age

Gender

Ann Arbor stage

IPI

LDH

β2-MG

Ferritin

0.458

0.112

0.559

0.004**

0.006**

0.843

0.060

0.782

0.776

1.020

1.806

3.070

2.460

1.000

1.043

1.000

0.398–1.516

0.995–1.045

0.394–3.493

1.430–6.593

1.292–4.683

1.000–1.000

0.998–1.090

1.000–1.000

   

Semi-quantitative parameters

ΔSUVmax(LLR)1

ΔTMTV1

ΔTLG1

0.000***

0.000***

0.000***

1.030

1.032

1.039

1.021–1.039

1.015–1.048

1.023–1.056

0.000***

0.004**

0.008**

1.024

1.026

1.030

1.013–1.035

1.008–1.044

1.008–1.053

ΔSUVmax(LLR)2

0.000***

1.007

1.003–1.011

   

ΔTMTV2

0.525

1.000

0.999–1.001

   

ΔTLG2

0.675

1.000

1.000–1.000

   

I-VA

CMR or non-CMR

0.000***

4.163

2.184–7.936

   

E-VA

CMR or non-CMR

0.000***

10.876

3.765–31.495

   
  1. ***p < 0.001, **p < 0.01, *p < 0.05
  2. PFS progression-free survival, HR Hazard Ratio, CI confidence interval, COO cell of origin, IPI international prognostic index, LDH lactate dehydrogenase, β2-MG β2-Microglobulin, SUVmax maximum standardized uptake value, LLR lesion-to-liver ratio calculated as SUVmax of the residual divided by SUVmax of the liver, TMTV total metabolic tumor volume, TLG total lesion glycolysis, VA visual analysis, CMR complete metabolic response, I interim, E end of treatment, 1 interim compared to baseline, 2 end of treatment compared to baseline