Table 3.
Summary of nintedanib-related toxicities
|
CTC grade, n (%) |
||||
---|---|---|---|---|---|
Patients with drug-related AEs, n (%) | 1 | 2 | 3 | 4 | Total |
Total |
18 (60) |
6 (20) |
2 (7) |
1 (3) |
27 (90) |
Gastrointestinal disorders |
16 (53) |
7 (23) |
0 |
0 |
23 (77) |
Nausea |
16 (53) |
4 (13) |
0 |
0 |
20 (67) |
Vomiting |
14 (47) |
2 (7) |
0 |
0 |
16 (53) |
Diarrhoea |
7 (23) |
5 (17) |
0 |
0 |
12 (40) |
Investigations |
2 (7) |
1 (3) |
2 (7) |
1 (3) |
6 (20) |
Hepatic enzyme increased |
0 |
1 (3) |
0 |
1 (3) |
2 (7) |
ALT increased |
0 |
1 (3) |
0 |
0 |
1 (3) |
AST increased |
0 |
1 (3) |
1 (3) |
0 |
2 (7) |
GGT increased |
0 |
1 (3) |
0 |
0 |
1 (3) |
CD4 decreased |
0 |
0 |
2 (7) |
0 |
2 (7) |
General disorders |
5 (17) |
0 |
0 |
0 |
5 (17) |
Fatigue | 5 (17) | 0 | 0 | 0 | 5 (17) |
Abbreviations: AE adverse event, ALT alanine aminotransferase, AST aspartate aminotransferase, CTC Common Toxicity Criteria, GGT gamma-glutamyl transpeptidase.