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. 2015 Jun;27(3):239–246. doi: 10.3978/j.issn.1000-9604.2015.06.08

Table 3. Occurrence of adverse events (n=9).

Adverse events N (%)
Grade 1 to 4 Grade 3 to 4
Hematologic toxicity
   Leukopenia 8 (88.9) 3 (33.3)
   Neutropenia 8 (88.9) 7 (77.8)
   Anemia 3 (33.3)
   Thrombocytopenia 1 (11.1)
Non-hematologic toxicity
   Cardiology
       Hypertension 3 (33.3)
   Dermatology
       Hand-foot syndrome 9 (100.0) 2 (22.2)
       Oral ulceration 1 (11.1)
       Oral mucositis 1 (11.1)
       Rash 1 (11.1)
   Infectious disease
       Fever 2 (22.2)
   GI
       Anorexia 8 (88.9)
       Nausea 6 (66.7)
       Vomiting 3 (33.3)
       Constipation 2 (22.2)
       Diarrhea 2 (22.2)
   Liver dysfunction
       ALT increase 2 (22.2) 1 (11.1)
       AST increase 1 (11.1) 1 (11.1)
       GGT increase 1 (11.1) 1 (11.1)
       Billirubin increase 1 (11.1) 1 (11.1)
   Others
       Neurotoxicity 1 (11.1)
       HTG 1 (11.1)
       α-HBDH increase 1 (11.1)
       LDH increase 1 (11.1)
       Alopecia 1 (11.1)
       Fatigue 1 (11.1)

GI, gastrointestinal; ALT, alanine aminotransferase; AST, aspartate aminotransferase; GGT, gamma-glutamyl transferase; HTG, hypertriglyceridemia; α-HBDH, α-hydroxybutyrate dehydrogenase; LDH, lactate dehydrogenase.