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Table 4 Pembrolizumab toxicity and management

From: A phase 2 study of combined chemo-immunotherapy with cisplatin-pembrolizumab and radiation for unresectable vulvar squamous cell carcinoma

Immune related Adverse Events (irAEs)

Toxicity grade (CTCAE V5.0)

Action with pembrolizumab

Corticosteroid and/or other therapies

Monitoring and follow-up

Pneumonitis

Grade 2

Withhold

Administer corticosteroids (initial dose of 1–2 mg/kg prednisone or equivalent) followed by taper

Add prophylactic antibiotics for opportunistic infections

Monitor participants for signs and symptoms of pneumonitis

Evaluate participants with suspected pneumonitis with radiographic imaging and initiate corticosteroid treatment

Grade 3 or 4, or recurrent Grade 2

Permanently discontinue

Diarrhea/Colitis

Grade 2 or 3

Withhold

Administer corticosteroids (initial dose of 1–2 mg/kg prednisone or equivalent) followed by taper

Monitor participants for signs and symptoms of enterocolitis (i.e., diarrhea, abdominal pain, blood or mucus in stool with or without fever) and of bowel perforation (i.e., peritoneal signs and ileus)

Participants with ≥ Grade 2 diarrhea suspecting colitis should consider GI consultation and performing endoscopy to rule out colitis

Participants with diarrhea/colitis should be advised to drink liberal quantities of clear fluids. If sufficient oral fluid intake is not feasible, fluid and electrolytes should be substituted via IV infusion

Grade 4 or recurrent Grade 3

Permanently discontinue

AST or ALT elevation or Increased Bilirubin

Grade 2a

Withhold

Administer corticosteroids (initial dose of 0.5–1 mg/kg prednisone or equivalent) followed by taper

Monitor with liver function tests (consider weekly or more frequently until liver enzyme value returned to baseline or is stable)

Grade 3b or 4c

Permanently discontinue

Administer corticosteroids (initial dose of 1–2 mg/kg prednisone or equivalent) followed by taper

Type 1 diabetes mellitus (T1DM) or Hyperglycemia

New onset T1DM or Grade 3 or 4 hyperglycemia associated with evidence of β–cell failure

Withholdd

Initiate insulin replacement therapy for participants with T1DM

Administer anti-hyperglycemic in participants with hyperglycemia

Monitor participants for hyperglycemia or other signs and symptoms of diabetes

Hypophysitis

Grade 2

Withhold

Administer corticosteroids and initiate hormonal replacements as clinically indicated

Monitor for signs and symptoms of hypophysitis (including hypopituitarism and adrenal insufficiency)

Grade 3 or 4

Withhold or permanently discontinued

Hyperthyroidism

Grade 2

Continue

Treat with non-selective beta-blockers (e.g., propranolol) or thionamides as appropriate

Monitor for signs and symptoms of thyroid disorders

Grade 3 or 4

Withhold or permanently discontinued

Hypothyroidism

Grade 2, 3, or 4

Continue

Initiate thyroid replacement hormones (e.g., levothyroxine or liothyronine) per standard of care

Monitor for signs and symptoms of thyroid disorders

Nephritis and renal dysfunction: grading according to increased creatinine or acute kidney injury

Grade 2

Withhold

Administer corticosteroids (prednisone 1–2 mg/kg or equivalent) followed by taper

Monitor changes of renal function

Grade 3 or 4

Permanently discontinue

Myocarditis

Grade 1 or 2

Withhold

Based on severity of AE administer corticosteroids

Ensure adequate evaluation to confirm etiology and/or exclude other causes

Grade 3 or 4

Permanently discontinue

All Other immune-related AEs

Intolerable/persistent Grade 2

Withhold

Based on severity of AE administer corticosteroids

Ensure adequate evaluation to confirm etiology or exclude other causes

Grade 3

Withhold or discontinue based on the evente

Grade 4 or recurrent Grade 3

Permanently discontinue

  1. a AST/ALT: > 3.0–5.0 × ULN if baseline normal; > 3.0–5.0 × baseline, if baseline abnormal; bilirubin: > 1.5–3.0 × ULN if baseline normal; > 1.5–3.0 × baseline if baseline abnormal
  2. b AST/ALT: > 5.0 to 20.0 × ULN, if baseline normal; > 5.0–20.0 × baseline, if baseline abnormal; bilirubin: > 3.0–10.0 × ULN if baseline normal; > 3.0 × 10.0 × baseline if baseline abnormal
  3. c AST/ALT: > 20.0 × ULN, if baseline normal; > 20.0 × baseline, if baseline abnormal; bilirubin: > 10.0 × ULN if baseline normal; > 10.0× baseline if baseline abnormal
  4. d The decision to withhold or permanently discontinue pembrolizumab is at the discretion of the investigator or treating physician. For participants with Grade 3 or 4 immune-related endocrinopathy where withhold of pembrolizumab is required, pembrolizumab may be resumed when AE resolves to ≤ Grade 2 and is controlled with hormonal replacement therapy or achieved metabolic control (in case of T1DM)
  5. e Events that require discontinuation include but are not limited to: Guillain–Barre Syndrome, encephalitis, Stevens-Johnson Syndrome and toxic epidermal necrolysis