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. 2024 Feb 3;13(3):897. doi: 10.3390/jcm13030897

Table 4.

Treatment-related adverse events.

Adverse Events Any Grade
n (%)
Grade 1–2
n (%)
Grade 3–4
n (%)
Non-haematological (patients, n = 55)
Diarrhea 28 (50.9) 25 (45.5) 3 (5.5)
Nausea 45 (81.8) 44 (80.0) 1 (1.8)
Vomiting 27 (49.1) 25 (45.5) 2 (3.6)
Dyspepsia 7 (12.7) 7 (12.7) 0 (0)
Constipation 22 (40.0) 20 (36.4) 2 (3.6)
Cystitis 9 (16.4) 9 (16.4) 0 (0)
Sensory neuropathy 41 (74.5) 39 (70.9) 2 (3.6)
Motor 22 (40.0) 20 (36.4) 2 (3.6)
Pain 42 (76.3) 39 (70.9) 3 (5.5)
Stomatitis 30 (54.5) 30 (54.5) 0 (0)
Skin 17 (30.9) 17 (30.9) 0 (0)
Nail disorder 7 (12.7) 6 (10.9) 1 (1.8)
Allergic reaction 7 (12.7) 5 (9.1) 2 (3.6)
Dyspnea 15 (27.3) 14 (25.5) 1 (1.8)
Fever in absence of infection 8 (14.5) 8 (14.5) 0 (0)
Fatigue 50 (90.9) 36 (65.5) 14 (25.5)
Anorexia 44 (80.0) 41 (74.5) 3 (5.5)
Myalgia 34 (61.8) 33 (60) 1 (1.8)
Arthralgia 27 (49.1) 27 (49.1) 0 (0)
Haematological (patients, n = 50)
Neutropenia 1 42 (84) 15 (30) 27 (54)
Thrombocytopenia 2 43 (86) 33 (66) 10 (20)
Anemia 3 45 (90) 45 (90) 0 (0)
Increased creatinine 5 (10) 5 (10) 0 (0)

1: The category of neutropenia includes reports of neutropenia and decreased neutrophil count. 2: The category of thrombocytopenia includes reports of thrombocytopenia and decreased platelet count. 3: The category of anemia includes reports of anemia and decreased hemoglobin count.