Table 2.
Management of immune-related adverse events induced by immune-checkpoint inhibitors.
irAE | ICIs Treatment | Management |
---|---|---|
Inflammatory Arthritis | anti-PD-1 and CTLA4 (Ipilimumab/Nivolumab) | Acetaminophen + oral corticosteroids of prednisone + intra-articular corticosteroid injection |
ICIs resumed | ||
Temporal Arteritis | anti-PD-L1 (Durvalumab) | Prednisone |
ICIs resumed pending clinical response | ||
Myocarditis | anti-PD-1 and CTLA4 (Ipilimumab + Nivolumab) | Methylprednisolone and diuretic treatment |
ICIs permanently discontinued | ||
Maculopapular Rash | anti-PD-L1 (Avelumab) | Betamethasone treatment+oral prednisone |
Resumed after symptom relief below grade 1 toxicity | ||
Nephritis | anti-PD-1 (Pembrolizumab) | Corticosteroids |
ICIs resumed after renal indices in a normal range | ||
Encephalitis | anti-PD-1 and CTLA4 (Ipilimumab + Nivolumab) | Pulse corticosteroids |
Resumed after neurological recovery | ||
Myasthenia Gravis | anti-PD-1 (Nivolumab) | Corticosteroids |
Permanently discontinued | ||
Uveitus | anti-PD-L1 (Atezolizumab) | Topical cycloplegic agent + prednisone |
Continued until corticosteroid reduction completed | ||
Pneumonitis | anti-PD-L1 (Durvalumab) | Dose-dependent corticosteroids according to different grade of checkpoint-inhibitor pneumonitis (CIP) |
Temporarily held during corticosteroid treatment in grade I and 2 CIP toxicity | ||
Hypophysitis | anti-PD-1 and CTLA4 (Ipilimumab + Nivolumab) | hydrocortisone +levothyroxine |
Resumed | ||
Hypothyroidism | anti-PD-L1 (Durvalumab) | levothyroxine |
Continued | ||
Thrombocytopenia | anti-PD-1 (Pembrolizumab) | Prednisone |
Resumed after 4 weeks treatment | ||
Colitis | anti-PD-1 and CTLA4 (Ipilimumab + Nivolumab) | Prednisone |
Resumed |
irAE, Immune-related adverse event; ICIs, Immune checkpoint inhibitors; anti-PD-1, anti-programmed cell death 1; CTLA4, Cytotoxic T lymphocyte protein 4; anti-PD-L1, anti-programmed cell death ligand 1; CIP, Checkpoint-inhibitor pneumonitis.