Table 3 Non-haematological and haematological treatment related adverse events

From: A phase I study of the safety and pharmacokinetics of the histone deacetylase inhibitor belinostat administered in combination with carboplatin and/or paclitaxel in patients with solid tumours

 

Cohort, n

 

Event or grade

1A

1B

2

3

4

Total (%)

Non-haematological

 Nausea

1–2

2

3

1

3

4

13 (57)

3

0

0

0

0

0

0

 Fatigue

1–2

1

4

1

2

3

11 (48)

3

0

0

0

1

0

1 (4)

 Vomiting

1–2

1

1

0

3

3

8 (35)

3

0

0

1

0

0

1 (4)

 Peripheral sensory neuropathy

1–2

0

3

0

1

2

6 (26)

3

0

0

1

1

0

2 (9)

 Alopecia

1–2

0

3

1

2

2

8 (35)

3

0

0

0

0

0

0

 Flushing

1–2

2

3

0

2

1

8 (35)

3

0

0

0

0

0

0

 Myalgia

1–2

0

3

1

1

2

7 (30)

3

0

0

1

0

0

1 (4)

 Arthralgia

1–2

0

3

1

1

1

6 (26)

3

0

0

0

0

0

0

Haematological

 Anaemia

1–2

5

4

2

3

3

17 (96)

3

0

0

0

0

1

1 (13)

 Leucopenia

1–2

2

4

1

3

2

12 (61)

3

0

0

0

3

2

5 (22)

 Neutropenia

1–2

2

1

2

0

6

11 (65)

3

1

0

0

2

0

3 (13)

4

0

0

0

1

2

3 (13)

 Thrombocytopenia

1–2

1

2

1

1

1

6 (48)

3

1

0

0

1

1

3 (13)