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Table 2 Adverse Events graded based on CTCAE 4.0

From: Multicenter phase II study of Apatinib in non-triple-negative metastatic breast cancer

Adverse event

Grade 1* (n, %)

Grade 2 (n, %)

Grade 3 (n, %)

Total

Hand-foot syndrome

4(10.5)

12(31.6)

4(10.5)

20(52.6)

Proteinuria

5(13.2)

13(34.2)

2(5.3)

20(52.6)

Hypertension

1(2.6)

7(18.4)

8(21.1)

16(42.1)

Pain

7(18.4)

4(10.5)

1(2.6)

12(31.6)

Neutropenia

4(10.5)

4(10.5)

1(2.6)

9(23.7)

Bilirubin increased

2(5.3)

5(13.2)

-

7(18.4)

Transaminase increased

5(13.2)

1(2.6)

1(2.6)

7(18.4)

Fatigue

3(7.9)

2(5.3)

1(2.6)

6(15.8)

Mucositis

-

5(13.2)

1(2.6)

6(15.8)

Thrombocytopenia

4(10.5)

1(2.6)

-

5(13.2)

Hematuria

4(10.5)

-

-

4(10.5)

Anorexia

-

2(5.3)

1(2.6)

3(7.9)

Dizziness

2(5.3)

1(2.6)

-

3(7.9)

Fever

2(5.3)

-

-

2(5.3)

Diarrhea

1(2.6)

1(2.6)

-

2(5.3)

Skin ulceration

-

1(2.6)

1(2.6)

2(5.3)

Vomiting

1(2.6)

-

-

1(2.6)

Ventricular arrhythmia

1(2.6)

-

-

1(2.6)

Dyspnea

-

1(2.6)

-

1(2.6)

  1. *According to CTCAE 4.0.