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Table 3 Comparison of treatment-related adverse events between the modified XELOX and standard XELOX groups

From: Safety and efficacy of a modified XELOX adjuvant regimen for patients with operated stage III colon cancer: a Chinese single-center experience

Adverse events

standard XELOX

(n = 126, %)

modified XELOX

(n = 84, %)

P value

Neurotoxicity

 Total

96 (76.2)

33 (39.3)

< 0.001

  Grade 1

61 (48.4)

20 (23.8)

< 0.001

  Grade 2

31 (24.6)

11 (13.1)

0.041

  Grade 3–4

4 (3.2)

2 (2.4)

0.311

Leucopenia

 Total

88 (69.8)

45 (53.6)

0.017

  Grade 1

56 (44.4)

29 (34.5)

0.196

  Grade 2

22 (17.5)

10 (11.9)

0.329

  Grade 3–4

10 (7.9)

6 (7.1)

0.832

Thrombocytopenia

 Total

75 (59.5)

32 (38.1)

0.011

  Grade 1

45 (35.7)

17 (20.2)

0.016

  Grade 2

26 (20.6)

12 (14.3)

0.242

  Grade 3–4

4 (3.2)

3 (3.6)

0.592

Nausea/vomiting

 Total

46 (36.5)

26 (31.0)

0.861

  Grade 1

27 (21.4)

13 (15.5)

0.221

  Grade 2

18 (14.3)

10 (11.9)

0.683

  Grade 3–4

1 (0.8)

3 (3.6)

0.149

Diarrhea

 Total

17 (13.5)

11 (13.1)

0.934

  Grade 1

9 (7.1)

7 (8.3)

0.794

  Grade 2

5 (4.0)

3 (3.6)

0.883

  Grade 3–4

3 (2.4)

1 (1.2)

0.536

Hand-foot syndrome

 Total

50 (39.7)

23 (27.4)

0.067

  Grade 1

32 (25.4)

15 (17.9)

0.238

  Grade 2

13 (10.3)

5 (6.0)

0.128

  Grade 3–4

5 (4.0)

3 (3.6)

0.251

Hepatic disorder

 Total

46 (36.5)

22 (26.2)

0.134

  Grade 1

34 (27.0)

17 (20.2)

0.325

  Grade 2

10 (7.9)

4 (4.8)

0.414

  Grade 3–4

2 (1.6)

1 (1.2)

0.817

  1. XELOX oxaliplatin and capecitabine regimen
  2. The listed grades of peripheral sensory neurotoxicity represent the maximal levels at any time