Table 2.
Patients with adverse events, no (%)* | ||
Any grade | Grade 3–4 | |
All causality AEs | 41 (98) | 8 (19) |
Treatment-related AEs | 33 (79) | 8 (19) |
Related to SIRT | 21 (50) | 2 (5) |
Related to nivolumab (IMAE) | 27 (64) | 6 (14) |
All causality SAEs | 21 (50) | 11 (26) |
Treatment-related SAEs | 5 (12) | 5 (12) |
Related to SIRT | 1 (2) | 1 (2) |
Related to Nivolumab (IMAE) | 4 (9) | 4 (9) |
AEs of special interest with incidence >10% | ||
Hepatic | 30 (71) | 8 (19) |
Blood | 16 (38) | 0 |
Gastrointestinal | 16 (38) | 3 (7) |
Skin | 12 (29) | 0 |
Endocrine | 10 (24) | 2 (5) |
*AEs and SAEs are reported separately.
AE, adverse event; SAEs, serious AEs; SIRT, selective internal radiation therapy.