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Table 2 Comparison of adverse events in the sorafenib and sunitinib groups

From: Comparison of efficacy, safety, and quality of life between sorafenib and sunitinib as first-line therapy for Chinese patients with metastatic renal cell carcinoma

Adverse event

Sorafenib group [cases (%)]

Sunitinib group [cases (%)]

P value*

All grade

Grade 1–2

Grade 3–4

All grade

Grade 1–2

Grade 3–4

Hypertension

23 (20.9)

22 (20.0)

1 (0.9)

23 (36.0)

20 (32.4)

3 (3.6)

0.050

Hand–foot syndrome

74 (67.3)

66 (60.0)

8 (7.3)

44 (59.5)

44 (59.5)

0 (0.0)

0.279

Diarrhea

69 (62.7)

67 (60.9)

2 (1.8)

26 (35.2)

23 (31.1)

3 (4.1)

<0.001

Nausea

41 (37.3)

41 (37.3)

0 (0.0)

29 (39.2)

29 (39.2)

0 (0.0)

0.793

Fatigue

42 (38.2)

42 (38.2)

0 (0.0)

33 (44.6)

33 (44.6)

0 (0.0)

0.385

Alopecia

9 (8.2)

9 (8.2)

0 (0.0)

7 (9.5)

7 (9.5)

0 (0.0)

0.763

Leukocytopenia

12 (10.9)

12 (10.9)

0 (0.0)

27 (36.5)

24 (32.4)

3 (4.1)

<0.001

Anemia

20 (18.2)

18 (16.4)

2 (1.8)

9 (12.2)

9 (12.2)

0 (0.0)

0.272

Thrombocytopenia

12 (10.9)

12 (10.9)

0 (0.0)

30 (40.5)

28 (37.8)

2 (2.7)

<0.001

Hypothyroidism

4 (3.6)

4 (3.6)

0 (0.0)

13 (17.6)

13 (17.6)

0 (0.0)

0.001

Elevation of ALT

11 (10.0)

10 (9.1)

1 (0.9)

10 (13.5)

10 (13.5)

0 (0.0)

0.462

  1. ALT alanine aminotransferase
  2. * Grade 1–2 and grade 3–4 toxicities were combined for the comparison