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. 2018 Jul 5;98(1):131–142. doi: 10.1007/s00277-018-3418-2

Table 2.

Adverse events regardless of causality occurring in ≥ 10% of patients

Adverse event All grades, n (%) Grade 3/4, n (%)
Hematologic toxicities
 Lymphopenia 48 (100) 46 (96)
 Leukopenia 35 (73) 20 (42)
 Neutropenia 27 (56) 17 (35)
 Thrombocytopenia 23 (48) 12 (25)
 Anemia 23 (48) 11 (23)
 Febrile neutropenia 6 (13) 6 (13)
Non-hematologic toxicities
 Constipation 13 (27) 1 (2)
 Nasopharyngitis 13 (27) 0 (0)
 Hypoalbuminemia 12 (25) 2 (4)
 Edema 12 (25) 0 (0)
 Pyrexia 11 (23) 1 (2)
 Stomatitis 11 (23) 1 (2)
 Headache 11 (23) 0 (0)
 Insomnia 10 (21) 0 (0)
 Alanine aminotransferase increased 10 (21) 1 (2)
 Nausea 9 (19) 1 (2)
 Decreased appetite 9 (19) 4 (8)
 Malaise 8 (17) 0 (0)
 Aspartate aminotransferase increased 8 (17) 0 (0)
 Rash 8 (17) 0 (0)
 Abnormal hepatic function 7 (15) 3 (6)
 Herpes zoster 7 (15) 1 (2)
 Pruritus 7 (15) 0 (0)
 Protein in urine 7 (15) 0 (0)
 Vomiting 6 (13) 0 (0)
 Cytomegalovirus infection 5 (10) 0 (0)
 Pneumonia 5 (10) 4 (8)
 Hyponatremia 5 (10) 4 (8)
 Decreased weight 5 (10) 1 (2)