Table 3 Adverse events (n = 76).

From: A phase 2 study of intraperitoneal carboplatin plus intravenous dose-dense paclitaxel in front-line treatment of suboptimal residual ovarian cancer

Adverse events

Grade 2

Grade 3

Grade 4

Leukocytopenia

24 (31.6%)

44 (57.9%)

4 (5.3%)

Neutropenia

8 (10.5%)

37 (48.7%)

27 (35.5%)

Anaemia

24 (31.6%)

35 (46.1%)

8 (10.5%)

Thrombocytopenia

13 (17.1%)

12 (15.8%)

5 (6.6%)

Fatigue

8 (10.5%)

1 (1.3%)

Anorexia

11 (14.5%)

2 (2.6%)

Nausea

21 (27.6%)

2 (2.6%)

Vomiting

13 (17.1%)

-

Constipation

26 (34.2%)

2 (2.6%)

Diarrhoea

5 (6.6%)

-

Neuropathy (sensory)

15 (19.7%)

6 (7.9%)

Neuropathy (motor)

12 (15.8%)

2 (2.6%)

Arthralgia

4 (5.3%)

1 (1.3%)

Myalgia

4 (5.3%)

1 (1.3%)

Alopecia

46 (60.5%)

-

Thrombosis

1 (1.3%)

1 (1.3%)

Port-related adverse events

9 (11.8%)