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. 2020 Mar 18;52(3):907–916. doi: 10.4143/crt.2019.713

Table 4.

Safety profile (any adverse events with incidence > 1%)

RAD (n=146) PAD (n=145) p-value
Leukopenia 35 (24.0) 38 (26.1) > 0.05
Neutropenia 41 (28.1) 46 (31.6) > 0.05
Febrile neutropenia 12 (8.3) 9 (6.2) > 0.05
Anemia 30 (20.6) 29 (19.9) > 0.05
Thrombocytopenia 21 (14.4) 17 (11.7) > 0.05
Anorexia 43 (29.5) 47 (32.2) > 0.05
Mucositis 14 (9.6) 19 (13.1) > 0.05
Diarrhea 18 (12.4) 13 (9.0) > 0.05
Abdominal pain 9 (6.2) 7 (4.8) > 0.05
Constipation 24 (16.5) 26 (17.9) > 0.05
Alopecia 27 (18.5) 40 (27.4) > 0.05
Rash 4 (2.8) 4 (2.8) > 0.05
AST elevation 5 (3.5) 5 (3.5) > 0.05
ALT elevation 6 (4.2) 4 (2.8) > 0.05
Hypernatremia 8 (5.5) 11 (7.6) > 0.05
Hyperkalemia 12 (8.3) 13 (9.0) > 0.05
Hypercalcemia 8 (5.5) 8 (5.5) > 0.05
Hypophosphatemia 9 (6.2) 5 (3.5) > 0.05

Values are presented as number (%). Adverse events were graded according to National Cancer Institute–Common Terminology Criteria (CTCAE) ver. 4.03. RAD, ramosetron, aprepitant, and dexamethasone; PAD, palonosetron, aprepitant, and dexamethasone; AST, aspartate aminotransferase; ALT, alanine aminotransferase.