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. Author manuscript; available in PMC: 2019 Jun 1.
Published in final edited form as: Invest New Drugs. 2017 Oct 9;36(3):442–450. doi: 10.1007/s10637-017-0519-z

Table 3.

Most common (frequency ≥ 20%) treatment-related adverse events categorized by highest grade experienced per patient (N = 19)

All Grades Grade 1 Grade 2 Grade 3a Grade 4
Non-Hematological
Elevated AST 15 (79%) 10 2 3 0
Fatigue 15 (79%) 2 11 2 0
Nausea 14 (74%) 8 5 2 0
Elevated ALT 14 (74%) 10 2 2 0
Diarrhea 11 (58%) 9 2 0 0
Dysgeusia 9 (47%) 3 6 0 0
Rash 9 (47%) 9 0 0 0
Anorexia 8 (42%) 2 6 0 0
Oral Mucositis 7 (37%) 5 1 1 0
Vomiting 6 (32%) 3 1 2 0
Peripheral Edema 6 (32%) 3 3 0 0
Elevated Alkaline Phosphatase 5 (26%) 3 2 0 0
Fever 4 (21%) 4 0 0 0
Hematological
Anemia 17 (89%) 3 11 3 0
Lymphocytopenia 14 (74%) 2 6 5 1
Leukopenia 14 (74%) 2 8 4 0
Neutropenia 12 (63%) 0 3 6 3
Thrombocytopenia 12 (63%) 7 3 2 0
Hypophosphatemia 11 (58%) 1 10 0 0

AST: aspartate aminotransferase; ALT: alanine aminotransferase

a

Additional Grade 3 dyspnea observed by one patient