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. 2024 Jun 1;29(9):e1201–e1208. doi: 10.1093/oncolo/oyae097

Table 1.

Incidence of adverse events in 13 patients.

Adverse events n (%)
Grade ≥ 3
Any grade Grade 3 Grade 4
Hematologic toxicity
 Leukocytopenia 13 (100) 8 (61.5) 5 (38.5)
 Neutropenia 13 (100) 12 (92.3)
 Febrile neutropenia 1 (7.7) 1 (7.7)
 Anemia 9 (69.2) 2 (15.4)
Non-hematologic toxicity
 Diarrhea 5 (38.5) 1 (7.7)
 Pulmonary edema 1 (7.7) 1 (7.7)
 Hypertension 2 (15.4) 2 (15.4)
 Syncope 1 (7.7) 1 (7.7)
 Urinary tract obstruction 1 (7.7) 1 (7.7)
 Mucocutaneous infection 11 (84.6) 2 (15.4)
 Arthralgia 1 (7.7) 1 (7.7)
Grade 1/2* (*reported in ≥20% of patients)
 Alopecia 10 (76.9)
 Rash 5 (38.5)
 Nausea 6 (46.2)
 Gastralgia/gastritis 5 (38.5)
 Constipation 4 (30.8)
 Hypoalbuminemia 11 (84.6)
 Anorexia 4 (30.8)
 Pyrexia 3 (23.1)
 Peripheral edema 3 (23.1)
 Weight increased 5 (38.5)
 Aspartate aminotransferase increased 4 (30.8)
 Peripheral neuropathy 6 (46.2)
 Upper respiratory infection 7 (53.8)
 Pneumonitis 3 (23.1)