| SRS and Ipilimumab (n = 45) | SRS and Nivolumab (n = 35) | ||
---|---|---|---|---|
Grade 1 or 2 | Grade 3 | Grade 1 or 2 | Grade 3 | |
Number of patients with at least an adverse eventa | 31 (68%) | 11 (24%) | 20 (57%) | 6 (17%) |
Event | ||||
 Diarrhoea | 11 (24%) | 3 (7%) | 5 (14%) | 1 (3%) |
 Nausea or vomiting | 8 (18%) | 1 (2%) | 4 (12%) | 1 (3%) |
 Constipation | 5 (11%) | 0 | 2 (6%) | 0 |
 Increased AST and/or ALT levels | 4 (9%) | 2 (4%) | 4 (12%) | 2 (6%) |
 Fatigue | 12 (27%) | 3 (7%) | 6 (18%) | 2 (6%) |
 Endocrine immune disorders | 3 (7%) | 0 | 2 (6%) | 0 |
 Rash/Pruritus | 10 (22%) | 1 (2%) | 6 (18%) | 1 (3%) |
 Arthralgia | 5 (11%) | 0 | 3 (9%) | 0 |
 Muscle weakness right or left sided | 3 (7%) | 1 (2%) | 2 (6%) | 1 (3%) |
CNS event | ||||
 Headache | 8 (18%) | 2 (4%) | 4 (12%) | 1 (3%) |
 Hemorrhage | 3 (7%) | 1 (2%) | 2 (6%) | 1 (3%) |
 Seizure | 3 (7%) | 2 (4%) | 2 (6%) | 1 (3%) |
 Diziness | 4 (9%) | 0 | 2 (6%) | 0 |
Brain necrosis | 13 (29%) | 5 (11%) | 7 (20%) | 3 (9%) |
Discontinuation of treatment | 5 | Â | 3 | Â |