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Table 3 Summary of all-causality adverse events occurring in >2 patients in the ITT population during the study period*

From: Phase II study of axitinib with doublet chemotherapy in patients with advanced squamous non–small-cell lung cancer

Adverse event

Cisplatin + gemcitabine + axitinib (n = 38)

All grades

Grade ≥3

No.

%

No.

%

Nausea

16

42.1

  

Anaemia

12

31.6

3

7.9

Vomiting

11

28.9

2

5.3

Hypertension

10

26.3

5

13.2

Neutropaenia

9

23.7

5

13.2

Weight loss

9

23.7

0

0

Appetite loss

8

21.1

0

0

Fatigue

7

18.4

3

7.9

Asthenia

6

15.8

0

0

Leukopaenia

5

13.2

2

5.3

Diarrhoea

5

13.2

0

0

Reduced creatinine clearance

5

13.2

0

0

Alopecia

5

13.2

0

0

Thrombocytopaenia

4

10.5

0

0

Chest pain

4

10.5

0

0

Toxic nephropathy

4

10.5

0

0

Cough

4

10.5

0

0

Dyspnoea

4

10.5

0

0

Rash

4

10.5

0

0

Pulmonary cavitation

3

7.9

1

2.6

Haemoptysis

3

7.9

1

2.6

  1. ITT = intent-to-treat.
  2. *Study period comprised the treatment period plus 28-day follow-up period after the last dose of study drug.