Immune-Related Adverse Events for GI Toxicity - Colitis
Grades severity of colitis secondary to immune checkpoint inhibitor therapy.
Use in adult patients with colitis symptoms that developed while on treatment with immune checkpoint inhibitors.
Grade 1: Further diagnostic work-up not recommended.
Grade 2: Further diagnostic work-up is recommended as following:
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Blood studies: CBC, comprehensive metabolic panel, thyroid-stimulating hormone, erythrocyte sedimentation rate, C-reactive protein.
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Stool studies: culture, Clostridium difficile, parasite, cytomegalovirus (CMV) or other viral etiology, ova and parasite.
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Lactoferrin – aids in patient stratification to determine who needs more urgent endoscopy.
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Calprotectin – aids in follow up of disease activity.
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Screening for HIV, hepatitis A and B, and blood quantiferon for tuberculosis in patients at high risk for infections – aids in preparation of patients to start infliximab.
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Consider imaging (i.e., CT scan of abdomen and pelvis and gastrointestinal endoscopy with biopsy) – presence of ulceration can predict corticosteroid refractory disease, which may require early infliximab.
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Consider repeat endoscopy for patients who do not respond to immunosuppressive agents.
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Consider repeat endoscopy for disease monitoring when clinically indicated and when planning to resume therapy.
Grade 3-4:
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Above work-up for grade 2 colitis should be immediately completed for grade 3-4 colitis.
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Consider repeat endoscopy for patients who do not respond to immunosuppressive agents.
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Consider repeat endoscopy for disease monitoring only when clinically indicated and when planning to resume therapy.
ASCO guidelines for IRAE - colitis:
All patients:
Counsel all patients to be aware of and inform their health care provider immediately if they experience any of the following:
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Abdominal pain, nausea, cramping, blood or mucus in stool, or changes in bowel habits.
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Fever, abdominal distention, obstipation, or constipation.
For grade ≥2, consider permanently discontinuing CTLA-4 agents and may restart PD-1, PD- L1 agents if patient can recover to grade ≤1; concurrent immunosuppressant maintenance therapy should be considered only if clinically indicated in individual cases.
Grade 1:
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Continue ICPi (or, hold temporarily and resume if toxicity does not exceed grade 1).
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Monitor for dehydration; recommend dietary changes.
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Facilitate expedited phone contact with patient/caregiver.
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May obtain GI consult for prolonged grade 1 cases.
Grade 2:
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Should hold immune checkpoint inhibitor until symptoms recover to grade 1; can consider permanently discontinuing CTLA-4 agents and may restart PD-1, PD-L1 agents if patient can recover to grade ≤1.
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Concurrent immunosuppressant maintenance therapy (<10 mg prednisone equivalent dose) may be offered only if clinically indicated in individual cases.
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May include supportive care with medications such as loperamide if infection has been ruled out.
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Should consult with GI for grade ≥2.
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Administer corticosteroids, unless diarrhea is transient, starting with an initial dose of 1 mg/kg/day prednisone or equivalent.
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When symptoms improve to grade ≤1, taper corticosteroids over at least 4-6 weeks before resuming treatment, although resuming treatment while on low-dose corticosteroid may also be an option after an evaluation of the risks and benefits.
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Esophagogastroduodenoscopy/colonoscopy, endoscopy evaluation should be highly recommended for cases grade ≥2 to stratify for early infliximab treatment based on endoscopic findings and to determine safety of resuming PD-1, PD-L1 therapy.
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Can consider stool inflammatory markers (lactoferrin and calprotectin) in cases of grade ≥2 to differentiate functional vs inflammatory diarrhea, and use calprotectin to monitor treatment response if provider prefers.
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Repeat colonoscopy optional for cases of grade ≥2 to monitor disease activity for complete remission, especially if plan to resume ICPi.
Grade 3:
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Should consider permanently discontinuing CTLA-4 agents and may restart PD-1, PD-L1 agents if patient can recover to grade ≤1.
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Administer corticosteroids (initial dose of 1–2 mg/kg/day prednisone or equivalent).
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Consider hospitalization or outpatient facility if dehydration or electrolyte imbalance.
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If symptoms persist 3–5 days or recur after improvement, consider IV corticosteroid or noncorticosteroid (e.g. infliximab) treatment.
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Consider colonoscopy if patient on immunosuppression and at risk for opportunistic infections as an independent cause for diarrhea (i.e., CMV colitis) or if on anti-TNF or corticosteroid refractory.
Grade 4:
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Permanently discontinue treatment.
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Should admit patient when clinically indicated; patients managed as outpatients should be very closely monitored.
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Administer 1–2 mg/kg/day methylprednisolone or equivalent until symptoms improve to grade 1, and then start taper over 4–6 weeks.
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Consider early infliximab 5–10 mg/kg if symptoms refractory to corticosteroid within 2–3 days.
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Consider lower GI endoscopy if symptoms are refractory despite treatment or there is concern of new infections.
Additional considerations:
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Vedolizumab may be considered in patients refractory to infliximab and/or contraindicated to TNF-α blocker. Decision should be made on individual basis from GI and oncology evaluation. This is based on case series showing promising results.
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Patients with hepatitis and IRAE colitis are rare, and management should include permanently discontinuing immune checkpoint inhibitors and offering other immunosuppressant agents that work systemically for both conditions.
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Currently, enteritis alone as the cause of diarrhea is uncommon and requires small bowel biopsy to evaluate. It may be managed similar as colitis, including corticosteroid and/or infliximab, etc.
See Brahmer 2018 for full ASCO guidelines.