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. 2023 Nov 10;66:102303. doi: 10.1016/j.eclinm.2023.102303

Table 3.

Adverse events.

Adverse events, n (%) Any grade Grade 1-2 Grade 3 Grade 4
Any 33 (100) 19 (58)a
Malaise 21 (64) 21 (64)
Anorexia 21 (64) 16 (49) 5 (15)
Alopecia 19 (58) 19 (58)
Edema limbs 16 (48) 14 (42) 2 (6)
Stomatitis 13 (39) 12 (36) 1 (3)
Constipation 11 (33) 11 (33)
Aspartate aminotransferase increased 11 (33) 11 (33)
Weight loss 10 (30) 10 (30)
Alanine aminotransferase increased 8 (24) 7 (21) 1 (3)
Peripheral sensory/motor neuropathy 8 (24) 8 (24)
Fever 6 (18) 6 (18)
Weight gain 6 (18) 5 (15) 1 (3)
Diarrhea 5 (15) 5 (15)
Vomiting 5 (15) 5 (15)
Creatinine increased 5 (15) 5 (15)
Pleural effusion 5 (15) 5 (15)
Hypoalbuminemia 4 (12) 4 (12)
Hyponatremia 4 (12) 1 (3) 3 (9)
Dysgeusia 4 (12) 4 (12)
Pneumonitis 4 (12) 1 (3) 3 (9)
Rash maculo-papular 4 (12) 4 (12)
Thrombocytopenia 22 (67) 21 (64) 1 (3)
Anemia 18 (55) 16 (48) 2 (6)
Neutropenia 13 (39) 5 (15) 4 (12) 4 (12)
White cell count decreased 9 (27) 8 (24) 1 (3)
Febrile neutropenia 3 (9) 3 (9)
Bleeding or hemorrhage 11 (33) 9 (27) 2 (6)
 Oral hemorrhage 1 (3) 1 (3)
 Epistaxis 7 (21) 7 (21)
 Pulmonary hemorrhage events 2 (6) 1 (3) 1 (3)
 Gastrointestinal hemorrhage 1 (3) 1 (3)
Proteinuria 8 (24) 7 (21) 1 (3)
Hypertension 13 (39) 11 (33) 2 (6)
Arterial/Venous thromboembolic event 0 (0) 0 (0) 0 (0)

AE; adverse event.

a

19 (58%) patients developed grade 3 or 4 AE. No grade 5 AEs was observed.