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. 2020 Nov 8;26(3):e382–e393. doi: 10.1002/onco.13574

Table 2.

Treatment‐related adverse events (n = 67)

Adverse event a Grade 2, n (%) Grade 3, n (%) Grade 4, n (%)
Hematological AEs 14 (21) 40 (60) 11 (16)
Neutropenia 19 (28) 26 (39) 11 (16)
Leukopenia 35 (52) 10 (15) 1 (1)
Anemia 29 (43) 29 (43) 0
Thrombocytopenia 8 (12) 8 (12) 0
Lymphopenia 10 (15) 5 (7) 0
Febrile neutropenia 0 2 (3) 0
Nonhematological AEs 34 (51) 12 (18) 0
Fatigue 23 (34) 5 (7) 0
Alopecia 16 (24) 0 0
Hypertension 8 (12) 0 0
Nausea/vomiting 6 (9) 0 0
Peripheral sensory neuropathy 3 (4) 5 (7) 0
Upper respiratory infection 3 (4) 0 0
Hypokalemia 2 (3) 1 (1) 0
Urinary tract infection 1(1) 1(1) 0
Dehydration 0 1 (1) 0
Hyperglycemia 0 1 (1) 0
Hyponatremia 0 1 (1) 0
Premature menopause 0 1 (1) 0
Hypophosphatemia 4 (6) 0 0
Depression 3 (4) 0 0
Oral mucositis 3 (4) 0 0
Elevated alanine transferase 2 (3) 0 0
Dyspnea 2 (3) 0 0
Hypocalcemia 2 (3) 0 0
a

Includes events with at least two grade 2 occurrences or one grade 3 or higher. Only the highest grade per person for each category is counted.

Abbreviation: AE, adverse event.