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. 2023 Aug 15;13(8):3582–3590.

Table 3.

Summary of adverse events

Toxicity Number of patients (BEAV) N=20 (%) Number of patients (Non BEAV) N=21 (%)


Any grade Grade 3-4 Any grade Grade 3-4
Summary 20 (100%) 11 (55.0%) 21 (100%) 8 (38.1%)
Hypertension 12 (60.0%) 1 (5.0%) 7 (33.3%) 1 (4.8%)
Thrombocytopenia 10 (50.0%) 1 (5.0%) 6 (28.6%) 0 (0%)
Fatigue 9 (45.0%) 0 (0%) 6 (28.6%) 1 (4.8%)
Abnormal liver function 8 (40.0%) 1 (5.0%) 9 (42.9%) 1 (4.8%)
Nausea 7 (35.0%) 0 (0%) 5 (23.8%) 0 (0%)
Mucosal inflammation 7 (35.0%) 1 (5.0%) 7 (33.3%) 0 (0%)
Anemia 7 (35.0%) 1 (5.0%) 6 (28.6%) 1 (4.8%)
Proteinuria 6 (30.0%) 1 (5.0%) 5 (23.8%) 0 (0%)
Thrombocytopenia 6 (30.0%) 0 (0%) 6 (28.6%) 0 (0%)
Diarrhea 6 (30.0%) 1 (5.0%) 5 (23.8%) 1 (4.8%)
Vomiting 6 (30.0%) 0 (0%) 5 (23.8%) 1 (4.8%)
Asthenia 6 (30.0%) 1 (5.0%) 7 (33.3%) 0 (0%)
Abdominal pain 6 (30.0%) 1 (5.0%) 8 (38.1%) 0 (0%)
Constipation 5 (25.0%) 0 (0%) 4 (19.0%) 1 (4.8%)
Skin rash 5 (25.0%) 1 (5.0%) 4 (19.0%) 0 (0%)
Leukopenia 5 (25.0%) 0 (5.0%) 4 (19.0%) 0 (0%)
Pain in extremity 5 (25.0%) 0 (0%) 3 (12.8%) 0 (0%)
Epistaxis 4 (20.0%) 0 (0%) 2 (9.5%) 1 (4.8%)
Gastrointestinal perforation 1 (5.0%) 1 (5.0%) 0 (0%) 0 (0%)