Table 2.
Adverse events attributed to adavosertib.
Adverse event | Grade 1-2 (%) | Grade 3 (%) | Grade 4 (%) |
---|---|---|---|
Hematological | |||
Anemia | 20 (47%) | 9 (21%) | — |
Leukopenia | 12 (29%) | 5 (12%) | 4 (10%) |
Lymphopenia | 18 (43%) | 12 (29%) | — |
Neutropenia | 5 (12%) | 4 (10%) | 5 (12%) |
Febrile neutropenia | — | 1 (2%) | — |
Thrombocytopenia | 13 (31%) | 5 (12%) | 1 (2%) |
Gastrointestinal | |||
Anorexia | 17 (40%) | — | — |
Diarrhea | 25 (60%) | 2 (5%) | — |
Nausea | 31 (74%) | 3 (7%) | — |
Vomiting | 24 (57%) | 5 (12%) | — |
Electrolyte | — | ||
Hypocalcemia | 3 (7%) | 1 (2%) | — |
Hypomagnesemia | 7 (17%) | 1 (2%) | — |
Hyponatremia | 8 (19%) | 1 (2%) | — |
Hypophosphatemia | 10 (24%) | 6 (14%) | — |
Hypokalemia | 5 (12%) | 1 (2%) | |
Infection | |||
Upper respiratory infection | — | 1 (2%) | — |
Investigations | |||
Alanine aminotransferase increased | 11 (26%) | — | — |
Aspartate aminotransferase increased | 11 (26%) | — | — |
Other | |||
Fatigue | 19 (45%) | 3 (7%) | — |
Dehydration | 5 (12%) | 1 (2%) | — |
Hypoalbuminemia | 9 (21%) | — | — |
The percentage of patients experiencing each event is noted in parentheses (n = 42 patients).