Clinical AEs and DLTs during treatment of the SACRED trial participants who received hydroxyurea treatment for conditional TCD velocities
. | Total . |
---|---|
Patient-years | 343 |
AEs | 566 |
Participants with AEs | 73 |
Grade 2 | 388 |
Grade 3 | 178 |
Grade 4 | 0 |
Rate per patient-year | 1.6 |
Grade 3-4 rate per patient-year | 0.5 |
SAEs | 37 |
Participants with SAEs | 23 |
Grade 2 | 1 |
Grade 3 | 30 |
Grade 4 | 5 |
Grade 5 | 1 |
SAE rate per patient-year | 0.1 |
DLTs | 312 |
Participants with DLTs | 57 |
Anemia | 116 |
Neutropenia | 17 |
Reticulocytopenia | 177 |
Thrombocytopenia | 2 |
Total CBC | 2462 |
CBC with DLT, n (%) | 243 (10) |
. | Total . |
---|---|
Patient-years | 343 |
AEs | 566 |
Participants with AEs | 73 |
Grade 2 | 388 |
Grade 3 | 178 |
Grade 4 | 0 |
Rate per patient-year | 1.6 |
Grade 3-4 rate per patient-year | 0.5 |
SAEs | 37 |
Participants with SAEs | 23 |
Grade 2 | 1 |
Grade 3 | 30 |
Grade 4 | 5 |
Grade 5 | 1 |
SAE rate per patient-year | 0.1 |
DLTs | 312 |
Participants with DLTs | 57 |
Anemia | 116 |
Neutropenia | 17 |
Reticulocytopenia | 177 |
Thrombocytopenia | 2 |
Total CBC | 2462 |
CBC with DLT, n (%) | 243 (10) |
CBC, complete blood count; DLTs, dose-limiting toxicities.