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. 2021 Dec 25;9(1):7–11. doi: 10.1016/j.apjon.2021.12.007

Table 2.

Summary of irAE treatment.6,12

Common adverse reactions Research of alternative/noninflammatory etiologies Degree of toxicity Recommended management of irAEs
Gastrointestinaldiarrhea/colitis Exclude infectious etiology (Clostridium difficile) Grade 1 (Mild) Symptomatic treatment
Consider budesonide 9 ​mg/day
Continue immunotherapy
Grade 2 (Moderate) Delay immunotherapy
Methylprednisolone IV 0.5–1 ​mg/kg/day (or oral equivalent)
Consider gastroenterology and colonoscopy consultation
When improving to ​≤ ​grade 1, reduce the dose for at least 4 weeks
Grades 3–4 (Severe) Stop immunotherapy
Methylprednisolone IV 1–2 ​mg/kg/day
When improving to ​≤ ​grade 1, reduce the dose for at least 4 weeks
If no improvement in symptoms within 48–72 ​h, consider 2nd-line immunosuppression (infliximab)
Hepatitis Evaluate for
  • -

    Alcohol intake

  • -

    Concomitant drugs with hepatotoxic potential

  • -

    Exclude biliary disease/biliary obstruction

Grade 1 (Mild) Continue immunotherapy
Repeat LFTs within 1 week
Grade 2 (Moderate) Delay immunotherapy
Repeat LFTs every 3–5 days
Methylprednisolone IV 0.5–1 ​mg/kg/day (or oral equivalent)
When improving to mild or baseline, reduce the dose of steroids for at least 4 weeks
Grades 3–4 (Severe) Stop immunotherapy
Increase the frequency of LFTs to 1–2 days
Methylprednisolone IV 1–2 ​mg/kg/day
Gastroenterology consultation
If no improvement in symptoms within 48–72 ​h, consider 2nd-line immunosuppression (infliximab)
Pneumonitis Evaluate for
  • -

    Pulmonary embolism

  • -

    Cardiac causes

  • -

    Infectious etiology

  • -

    COPD

  • -

    Seasonal allergies/cough post-nasal drip

Grade 1 (Mild) Delay immunotherapy
Monitor symptoms
Repeat chest X-ray in 2–4 weeks
Grade 2 (Moderate) Delay immunotherapy
Monitor symptoms closely, consider hospitalization
Reimage every 1–3 days
Pneumology and infectious disease consultations, consider bronchoscopy
Methylprednisolone IV 1–2 ​mg/kg/day (or oral equivalent)
When symptoms improve, reduce the dose of steroids for at least 4 weeks
Grades 3–4 (Severe) Stop immunotherapy
Methylprednisolone IV 2–4 ​mg/kg/day, discontinue steroids for a period of at least 6 weeks
If no improvement in symptoms within 48–72 ​h, consider 2nd-line immunosuppression (infliximab, mycophenolate mofetil, IVIG)
Dermatological adverse reactions Exclude noninflammatory causes (allergic reaction to other drugs, photosensitivity, etc.) Grade 1 (Mild) Continue immunotherapy
Supportive therapy emollients, low-potency topical steroids, antihistamines
Grade 2 (Moderate) Continue immunotherapy
Topical steroids of moderate-high potency
If persistent, despite optimized topical treatment, consider methylprednisolone 0.5–1 ​mg/kg/day (or oral equivalent)
If it improves slightly or resolves, reduce the dose of steroids for at least 4 weeks
Consider dermatological evaluation and skin biopsy
Grades 3–4 (Severe) Delay immunotherapy
Methylprednisolone IV 1–2 ​mg/kg/day (or oral equivalent)
If it improves to mild or resolves, reduce the dose of steroids for at least 4 weeks.
Consider skin biopsy
Endocrinopathies Exclude noninflammatory etiology of symptoms Grade 1 (Mild) Continue immunotherapy
If TSH is abnormal, add free T4 and T3
Consider morning cortisol and ACTH
Grade 2 (Moderate) TSH, free T4, morning cortisol and ACTH Consider pituitary MRI Methylprednisolone IV 1–2 ​mg/kg/day (or oral equivalent) If it improves, reduce the dose of steroids for at least 4 weeks
Hormone replacement therapy if indicated
Endocrinology consultation
Grades 3–4 (Severe) Delay or discontinue immunotherapy
If adrenal crisis is suspected, exclude infection/sepsis, BP support
Stress doses of mineralocorticosteroid

ACTH, adrenocorticotrophin; COPD, chronic obstructive pulmonary disease; GI, gastrointestinal; IVIG, intravenous immunoglobulin; IV, intravenous; MRI, magnetic resonance image; BP, blood pressure; T3, triiodothyronine; T4, thyroxine; LFTs, liver function tests; TSH, thyroid-stimulating hormone; irAEs, immune-related adverse effects.