Table 6 Uni- and multivariate association of CDR1-AS, hsa-miR-7 and other clinical variables with PFS in the predictive cohort.

From: Association of microRNA-7 and its binding partner CDR1-AS with the prognosis and prediction of 1st-line tamoxifen therapy in breast cancer

Parameters base model

univariate model

multivariate model

n

HR

(95% CI)

P

HR

(95% CI)

P

 

188

      

Age at start 1 st -line tamoxifen

≤55 years

75

1

  

1

  

56–70 years

67

0.76

(0.54–1.07)

0.11

0.78

(0.54–1.13)

0.19

>70 years

46

0.57

(0.38–0.84)

0.005

0.65

(0.43–0.98)

0.039

Disease-free interval

≤1 year

76

1

  

1

  

1–3 years

48

0.79

(0.54–1.14)

0.21

0.83

(0.56–1.22)

0.34

>3 years

64

0.68

(0.48–0.97)

0.032

0.74

(0.51–1.05)

0.09

Dominant site of relapse

Local regional

21

1

  

1

  

Bone

101

1.60

(0.96–2.65)

0.071

1.99

(1.16–3.43)

0.013

Other distant metastasis

66

1.34

(0.78–2.27)

0.28

2.00

(1.10–3.63)

0.023

Hormone/growth factor receptors*

ER (log continuous ESR1)

188

0.77

(0.67–0.89)

<0.001

0.82

(0.69–0.96)

0.016

PR (log continuous PGR)

188

0.89

(0.83–0.96)

0.002

0.92

(0.84–0.96)

0.038

HER2 (ERBB2) status

  Not amplified

165

1

  

1

  

  Amplified

23

1.86

(1.19–2.90)

0.007

1.49

(0.89–2.50)

0.13

     

hsa-miR-7 separately added to the base model

CDR1-AS (log continuous)

188

0.97

(0.86–1.10)

0.62

   

hsa-miR-7 (log continuous)

188

1.18

(1.04–1.33)

0.008

1.22

(1.08–1.38)

0.002

≤median

94

1

  

1

  

>median

94

1.54

(1.14–2.09)

0.005

1.63

(1.18–2.25)

0.003

  1. This table shows the associations of PFS with the cohort characteristics and CDR1-AS and hsa-miR-7 expression. The different metrics were examined with an univariate analysis on the left side of the table, while they were analysed with a multivariate model on the right side. n = number of patients, HR = hazard ratio, CI = confidence interval, and P = p-value. Significant p-values are printed in bold. The hormone/growth factor receptor expression values used in this table were determined by qPCR. *Cut-offs for positive and negative hormone/growth factor status were established as previously described56,57.