Table 3 Association of baseline characteristics and response parameters with the probability of achieving major histopathologic response

From: Differential histopathologic parameters in colorectal cancer liver metastases resected after triplets plus bevacizumab or cetuximab: a pooled analysis of five prospective trials

   

Univariate analysis

Multivariate analysis

 

N

%

OR

95% CI

p

OR

95% CI

p

Baseline characteristics

  Sex

    Male

97

23.7

1

    Female

62

29.0

1.32

0.64–2.71

0.454

  Time to metastases

    Synchronous

131

25.2

1

    Metachronous

28

28.6

1.88

0.48–2.95

0.708

  No. of liver metastases

    ≥4

59

27.1

1

    <4

74

28.4

1.06

0.50–2.29

0.862

  Primary resected

    No

38

36.8

1

    Yes

120

22.5

0.50

0.23–1.09

0.079

  Location of primary

    Right colon

40

27.5

1

    Left colon

116

25.0

0.88

0.39–1.98

0.752

  Tumour size, diameter

    >5 cm

56

32.1

1

    ≤5 cm

102

22.5

0.61

0.30–1.27

0.188

  Distribution of liver metastases

    Bilobar

96

19.8

1

    Unilobar

54

29.6

1.71

0.79–3.69

0.171

  No. of involved segments

    >6

14

35.7

1

    ≤6

121

27.3

0.68

0.21–2.16

0.536

  Disease-free interval

    <12 mos

22

22.7

1

    >12 mos

137

26.3

1.21

0.42–3.52

0.729

  Mutational status

    All wt

91

19.8

1

    RAS mut

54

25.9

1.42

0.64–3.15

0.390

    BRAF mut

6

33.3

2.03

0.34–11.95

0.600

  Targeted agent

    Cetuximab

56

14.3

1

1

    Bevacizumab

103

32.0

2.83

1.20–6.65

0.015

6.00

1.96–18.40

0.002

  Chemotherapy backbone

    COI

67

14.9

1

1

    FOLFOXIRI

92

33.7

2.90

1.30–6.44

0.008

0.62

0.14–2.64

0.516

Response parameters

  RECIST response

    No

24

16.7

1

    Yes

135

27.4

1.89

0.60–5.89

0.267

  Early tumour shrinkage

    No

23

13.0

1

    Yes

126

28.6

2.67

0.75–9.53

0.119

  Deepness of response (per 10% increase)

121

1.31

1.07–1.60

0.009

1.52

1.38–1.94

<0.001

  1. The "p" in bold indicate the p value statistically significant