Table 1.
Immune-mediated adverse event | Manifestations | Management |
---|---|---|
Enterocolitis | Diarrhoea, abdominal pain, mucus or blood in stool | Antidiarrhoeals followed by systemic corticosteroids if persistent; infliximab if refractory |
Pneumonitis | Dyspnoea, cough | Systemic corticosteroids |
Hepatitis | ALT/AST, bilirubin elevation | Systemic corticosteroids; mycophenolate mofetil if refractory |
Dermatitis | Pruritic/macular/papular rash, Stevens–Johnson syndrome (rare), toxic epidermal necrolysis (rare) | Topical betamethasone or oral antihistamines; systemic corticosteroids if refractory |
Neuropathy | Sensory/motor neuropathy, Guillain–Barre syndrome (rare), myasthenia gravis (rare) | Systemic corticosteroids |
Endocrinopathy | Hypothyroidism, hyperthyroidism, hypopituitarism, adrenal insufficiency, hypogonadism, Cushing’s syndrome (rare) | Systemic corticosteroids, appropriate hormone replacement (potentially long-term) |
Other irAEs | Arthritis, nephritis, meningitis, pericardidits, uveitis, iritis, anaemia, neutropenia | Organ-system specific |
Severe immune-mediated adverse events require permanent discontinuation of therapy and initiation of high-dose systemic corticosteroids. Therapy should be withheld for moderate immune-mediated adverse events or symptomatic endocrinopathy. Non-immune aetiology should be ruled out when possible, and manufacturer recommendations should be reviewed for the latest guidance and dosing information. ALT, alanine aminotransferase; AST, aspartate aminotransferase; irAEs, immune-related adverse events.