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. 2020 Aug 5;126(20):4485–4497. doi: 10.1002/cncr.33067

Table 3.

Treatment‐Related AEs

AEs Pembrolizumab (n = 35), No. (%) Pembrolizumab + Acalabrutinib (n = 40), No. (%)
Any AEs related to acalabrutinib
Grade 1/2 11 (27.5)
Grade 3/4 8 (20.0)
Most frequent AEs related to acalabrutinib a
Fatigue 6 (15.0)
Nausea 2 (5.0)
Vomiting 2 (5.0)
Anemia 2 (5.0)
Decreased appetite 2 (5.0)
Diarrhea 2 (5.0)
Headache 2 (5.0)
Decreased platelet count 2 (5.0)
Any AEs related to pembrolizumab
Grade 1/2 23 (65.7) 11 (27.5)
Grade 3/4 7 (20) 9 (22.5)
Grade 5 0 1 (2.5)
Most frequent AEs related to pembrolizumab a
Fatigue 12 (34.3) 6 (15.0)
Decreased appetite 6 (17.1) 2 (5.0)
Diarrhea 3 (8.6) 5 (12.5)
Hypothyroidism 6 (17.1) 1 (2.5)
Rash, maculopapular 4 (11.4) 3 (7.5)
ALT increase 2 (5.7) 5 (12.5)
Rash 4 (11.4) 3 (7.5)
AST increase 1 (2.9) 5 (12.5)
Nausea 4 (11.4) 2 (5.0)
Pruritus 3 (8.6) 2 (5.0)
Vomiting 3 (8.6) 2 (5.0)
Anemia 2 (5.7) 2 (5.0)
Dry skin 2 (5.7) 2 (5.0)
Peripheral edema 1 (2.9) 3 (7.5)
Abdominal pain 1 (2.9) 2 (5.0)
Arthralgia 2 (5.7) 1 (2.5)
Cough 0 3 (7.5)
Dry mouth 2 (5.7) 1 (2.5)
Dyspnea 0 3 (7.5)
Infusion‐related reaction 2 (5.7) 1 (2.5)
Pneumonia 2 (5.7) 1 (2.5)
Pyrexia 2 (5.7) 1 (2.5)
Blood alkaline phosphatase increase 0 2 (5.0)

Abbreviations: AE, adverse event; ALT, alanine aminotransferase; AST, aspartate aminotransferase.

a

All grades; 2 or more patients.