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. 2023 Jun 24;9(7):FSO878. doi: 10.2144/fsoa-2023-0049

Table 7. . Immune-related adverse events reported in our cohort.

Type of iRAE Grade 1–2 Grade 3–4 Management of the AE
Temporary interruption Systemic steroids Permanent discontinuation
Skin AEs 16 (22.2%) 0 (0%) 3 (4.2%) 6 (8.3%) 1 (1.4%)
Diarrhea 8 (11.1%) 1 (1.4%) 4 (5.6%) 4 (5.6%) 0 (0%)
Hypothyroidism 8 (11.1%) 0 (0%) 0 (0%) 0 (0%) 0 (0%)
Hyperglycemia 2 (2.8%) 0 (0%) 0 (0%) 0 (0%) 0 (0%)
Liver enzyme elevation 6 (8.3%) 0 (0%) 0 (0%) 0 (0%) 0 (0%)
Pneumonia 1 (1.4%) 0 (0%) 0 (0%) 0 (0%) 0 (0%)
Asthenia 2 (2.8%) 0 (0%) 0 (0%) 0 (0%) 0 (0%)
Arthralgia 2 (2.8%) 0 (0%) 0 (0%) 1 (1.4%) 0 (0%)
Renal AEs 1 (1.4%) 1 (1.4%) 2 (2.8%) 2 (2.8%) 1 (1.4%)
Total patients 28 (38.9%) 2 (2.8%) 9 (12.5%) 12 (16.7%) 2 (2.8%)

AE: Adverse event.