Skip to main content
. 2023 Apr 20;12(12):13041–13053. doi: 10.1002/cam4.5978

TABLE 5.

Treatment‐related adverse events.

Toxicity Any grade Grade 3 Grade 4 Grade ≥3
Hematologic
Leukocytopenia 15 (51.7) 6 (20.7) 2 (6.9) 8 (27.6)
Neutropenia 16 (55.2) 4 (13.8) 5 (17.2) 9 (31.0)
Thrombocytopenia 2 (6.9) 0 0 0
Anemia 16 (55.2) 0 0 0
Febrile neutropenia 0 0 0 0
Nonhematologic
AST increase 4 (13.8) 1 (3.4) 0 1 (3.4)
ALT increase 4 (13.8) 1 (3.4) 0 1 (3.4)
Nausea 4 (13.8) 0 0 0
Anorexia 6 (20.7) 0 0 0
Joint pain 2 (6.9) 0 0 0
Myalgia 0 0 0 0
Peripheral sensory neuropathy 12 (41.4) 2 (6.9) 0 2 (6.9)
Alopecia 17 (58.6) 0 0 0
Rash 2 (6.9) 0 0 0
Interstitial lung disease 3 (10.3) 1 (3.4) 0 1 (3.4)
Fatigue 1 (3.4) 0 0 0
Paronychia 1 (3.4) 0 0 0
Creatinine increase 1 (3.4) 0 0 0
Tears 1 (3.4) 0 0 0
Eye disorders (macular edema) 1 (3.4) 0 0 0
Diarrhea 1 (3.4) 0 0 0
Bronchitis 1 (3.4) 0 0 0

Note: All values are given as n (%).

Abbreviations: ALT, alanine aminotransferase; AST, aspartate aminotransferase.