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Table 2 Comparison of the incidence of major drug-related grade 3 or 4 AEs between groups at final follow-up

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

AEs, n (%)

CET (n=100)

BEV (n=104)

P-value

Skin

21 (21.0)

5 (4.8)

0.001*

Diarrhoea

13 (13.0)

4 (5.4)

0.018*

Anorexia

5 (5.0)

1 (1.0)

0.088

Vomiting

7 (7.0)

1 (1.0)

0.026*

Stomatitis

5 (5.0)

3 (2.9)

0.436

Fatigue

9 (9.0)

2 (1.9)

0.025*

Thrombocytopenia

13 (13.0)

4 (3.8)

0.018*

Dysphonia

3 (3.0)

4 (3.8)

0.740

Proteinuria

10 (10.0)

3 (2.9)

0.038*

Nausea

8 (8.0)

2 (1.9)

0.044*

Hypoalbuminemia

8 (8.0)

7 (6.7)

0.728

Peripheral oedema

7 (7.0)

8 (7.7)

0.850

Hepatic encephalopathy

3 (3.0)

5 (4.8)

0.506

≥ 2 AEs in one patient

23 (22.0)

12 (11.5)

0.030*

  1. *Statistically significant. AEs Adverse events, CET Cetuximab, BEV Bevacizumab