Table 2 Adverse events according to Common Terminology Criteria for Adverse Events (CTCAE) v3.0

From: Phase II study of everolimus (RAD001) monotherapy as first-line treatment in advanced biliary tract cancer with biomarker exploration: the RADiChol Study

 

All grades

Grade 3 or 4

Adverse event

n (%)

n (%)

Stomatitis/oral mucositis

17 (63%)

2 (7%)

Pain

16 (59%)

4 (15%)

Rash

14 (52%)

1 (4%)

Nausea

12 (44%)

0 (0%)

Diarrhoea

12 (44%)

1 (4%)

Infections

11 (41%)

7 (26%)

Fatigue

10 (37%)

1 (4%)

Cough

9 (33%)

0 (0%)

Anorexia

8 (30%)

1 (4%)

Vomiting

8 (30%)

0 (0%)

Pruritus

7 (26%)

0 (0%)

Oedema

7 (26%)

0 (0%)

Hyperglycaemia

6 (22%)

3 (11%)

Weight loss

6 (22%)

0 (0%)

Epistaxis

6 (22%)

0 (0%)

Anaemia

5 (19%)

3 (11%)

Hypercholesterolaemia

5 (19%)

0 (0%)

Hypokalaemia

5 (19%)

1 (4%)

Taste alteration

4 (15%)

0 (0%)

Pneumonitis

4 (15%)

1 (4%)

Dry skin

4 (15%)

0 (0%)

Nail changes

4 (15%)

0 (0%)

Insomnia

4 (15%)

0 (0%)

Constipation

3 (11%)

1 (4%)

Headache

3 (11%)

0 (0%)

Neutropenia

2 (7%)

0 (0%)

Thrombocytopenia

2 (7%)

1 (4%)

Flu-like syndrome

2 (7%)

0 (0%)

Thromboembolism

2 (7%)

2 (7%)

Ocular toxicity

2 (7%)

0 (0%)