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. 2022 Apr 5;27(4):253–e312. doi: 10.1093/oncolo/oyab078

Table 3.

Treatment-related adverse events in all treated patients (n = 50).

Grade 1 Grade 2 Grade 3 Grade 4 Any grade
Number of patients (%) 10 (20.0) 20 (40.0) 8(16.0) 4 (8.0) 42 (84.0)
Number of events (%) 60 44 18 7 129
Hematological
 Neutropenia 3 (6.0) 4 (8.0) 5 (10.0) 3 (6.0) 15 (30.0)
 Leucopenia 4 (8.0) 12 (24.0) 6 (12.0) 3 (6.0) 25 (50.0)
 Anemia 10 (20.0) 7 (14.0) 1 (2.0) 0 18 (36.0)
 Thrombocytopenia 4 (8.0) 5 (10.0) 0 1 (2.0) 10 (20.0)
Non-hematological
 Appetite decrease 8 (16.0) 2 (4.0) 0 0 10 (20.0)
 Nausea and vomiting 4 (8.0) 1 (2.0) 0 0 5 (10.0)
 Diarrhea 3 (6.0) 1 (2.0) 5 (10.0) 0 9 (18.0)
 Abdominal distention 11 (22.0) 4 (8.0) 0 0 15 (30.0)
 Neurotoxicity 3 (6.0) 0 0 0 3 (6.0)
 Venous thrombosis 0 1 (2.0) 0 0 1 (2.0)
 Asthenia 9 (18.0) 4 (8.0) 1 (2.0) 0 14 (28.0)
 Alopecia 1 (2.0) 1 (2.0) 0 0 2 (4.0)
 Renal function abnormal 0 2 (4.0) 0 0 2 (4.0)