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Table 1 Patient demographics and baseline characteristics

From: Cetuximab versus bevacizumab following prior FOLFOXIRI and bevacizumab in postmenopausal women with advanced KRAS and BRAF wild-type colorectal cancer: a retrospective study

Variable

CET (n=100)

BEV (n=104)

P-value

Age at onset (years)

64.2±9.5

64.5±8.7

0.231

CRC locationa, n (%)

  

0.331

 Left

52 (52.0)

47 (45.2)

 

 Right

48 (48.0)

57 (54.8)

 

Metastatic sites, n (%)

  

0.848

 Intra-abdominal

25 (25.0)

27 (26.0)

 

 Lung

14 (14.0)

16 (15.4)

 

 Bone

22 (22.0)

26 (25.0)

 

 Live

25 (25.0)

17 (16.3)

 

 Brain

7 (7.0)

9 (8.7)

 

 Other

11 (11.0)

1413.5)

 

Serum lactate dehydrogenase level, n (%)

  

0.428

 Normalb

33 (33.0)

29 (27.9)

 

 Above normal

67 (67.0)

75 (72.1)

 

Portal vein invasion, n (%)

  

0.733

 Yes

67 (67.0)

72 (69.2)

 

 No

33 (33.0)

32 (30.8)

 

Duration of treatment (months)

27.2±11.4

27.3±12.5

0.106

Hepatic encephalopathy, n (%)

0 (0.0)

0 (0)

1.000

ECOG PS, n (%)

  

0.860

 0

43 (43.0)

46 (44.2)

 

 1

57 (57.0)

58 (55.8)

 

Number of metastatic sites, n (%)

  

0.454

 3

13 (13.0)

20 (19.2)

 

 > 3

72 (72.0)

68 (65.4)

 

 Unknown

15 (15.0)

16 (15.4)

 
  1. aTumours occurring from the cecum to the transverse colon were considered to be right-sided tumours, and those occurring from the splenic flexure to the sigmoid colon were considered to be left-sided tumours [20]. bUsing continuous monitoring method: female 100-230 U/L. CET Cetuximab, BEV Bevacizumab, CRC Colorectal cancer, ECOG PS Eastern Collaborative Oncology Group performance status