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. 2022 Jan 3;12:746707. doi: 10.3389/fphar.2021.746707

TABLE 3.

Summary of adverse events. Values are expressed as frequencies [n (%)].

Adverse event Osi + bev (n = 38) Che + bev (n = 58)
All grades Grade ≥ 3 All grades Grade ≥ 3
Proteinuria 13 (34.2) 3 (7.9) 17 (29.3) 5 (8.6)
Thrombocytopenia 12 (31.6) 3 (7.9) 15 (25.9) 11 (19)
Neutropenia 9 (23.7) 2 (5.3) 29 (50.0) 14 (24.1)
AST/ALT elevation 8 (21.1) 2 (5.3) 14 (24.1) 6 (10.3)
Hypoproteinemia 10 (26.3) 1 (2.6) 16 (27.6) 5 (8.6)
Anemia 7 (18.4) 3 (7.9) 13 (22.4) 7 (12.1)
Fatigue 8 (21.1) 0 19 (32.8) 10 (17.2)
Rash 7 (18.4) 0 2 (3.4) 0
Anorexia 8 (21.1) 2 (5.3) 15 (25.9) 6 (10.3)
Nausea 7 (18.4) 0 16 (27.6) 4 (6.9)
Vomiting 3 (7.9) 0 10 (17.2) 2 (3.4)
Headache 4 (10.5) 0 5 (8.6) 0
Oral mucositis 5 (13.2) 0 7 (12.1) 0
Pharyngodynia 3 (7.9) 0 6 (10.3) 0
Hypertension 11 (28.9) 5 (13.2) 18 (31) 6 (10.3)
Diarrhea 9 (23.7) 4 (10.5) 14 (24.1) 2 (3.4)
Bleeding 8 (21.1) 2 (5.3) 12 (20.7) 1 (1.7)

WBC, white blood cell; ALT, alanine aminotransferase; AST, aspartate aminotransferase; osi + bev, osimertinib plus bevacizumab; che + bev, chemotherapy plus bevacizumab.