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. 2023 Oct 24;14:6761. doi: 10.1038/s41467-023-42400-5

Table 3.

Incidence of treatment-related adverse events

Event Cases (31 (%))
Any event 27 (87.1)
Any serious event 18 (58.1)
Any event leading to discontinuation or withdrawal of ipilimumab only 1 (3.2)
Any event leading to temporary discontinuation or withdrawal of both trial drugs 15 (48.4)
Any treatment-related event leading to withdrawal of both study drugs 3 (9.7)
    Immune-related Hepatitis 2 (6.5)
    Immune-related Colitis 1 (3.2)
Any event leading to patient death 3 (9.7)
    Sepsis 2 (6.5)
    Suicide 1 (3.2)
Any event occurring in 10% of patients Any Grade Grade 3 or 4
    Infection or sepsis 10 (32.2) 6 (22.5)
    Nausea 6 (19.4) 1 (3.2)
    Renal impairment 6 (19.4) 2 (6.4)
    Anemia 5 (16.1) 0
    Vomiting 5 (16.1) 1 (3.2)
    Constipation 4 (12.9) 1 (3.2)
    Diarrhea 4 (12.9) 1 (3.2)
    Fatigue 4 (12.9) 0
    Deterioration of general condition 4 (12.9) 3 (9.7)
    Hypokalemia 4 (12.9) 3 (9.7)
Immune-related AEs 14 (45.2) 9 (29)
    Hepatitis 4 (12.9) 4 (12.9)
    Diarrhea / Colitis 3 (9.7) 3 (9.7)
    Hyperthyroidism 3 (9.7) 0
    Hypophysitis 1 (3.2) 1 (3.2)
    Arthritis 1 (3.2) 1 (3.2)
    Pruritus 1 (3.2) 0
    Fatigue 1 (3.2) 0

Source data are provided as a Source Data file.