Grade 3-4 AEs, AEs leading to treatment modifications, and supportive care
. | POM+LoDEX (n = 112) . | POM alone (n = 107) . |
---|---|---|
Hematologic AEs occurring in ≥5% of patients, % | ||
Neutropenia | 41 | 48 |
Anemia | 22 | 24 |
Thrombocytopenia | 19 | 22 |
Leukopenia | 10 | 7 |
Lymphopenia | 7 | 2 |
Febrile neutropenia | 3 | 5 |
Nonhematologic AEs occurring in ≥5% of patients, % | ||
Pneumonia | 22 | 15 |
Fatigue | 14 | 11 |
Dyspnea | 13 | 8 |
Back pain | 10 | 14 |
Urinary tract infection | 9 | 2 |
Sepsis | 5 | 6 |
Dehydration | 5 | 5 |
Acute renal failure | 5 | 8 |
Muscular weakness | 4 | 6 |
Blood creatinine increase | 3 | 6 |
Confusional state | 3 | 7 |
Hypercalcemia | 1 | 10 |
AEs leading to dose reduction in ≥5% of patients, % | ||
Thrombocytopenia | 5 | 9 |
Neutropenia | 4 | 7 |
AEs leading to dose interruption in ≥5% of patients, % | ||
Neutropenia | 9 | 14 |
Thrombocytopenia | 5 | 11 |
Pneumonia | 18 | 12 |
Upper respiratory tract infection | 5 | 9 |
Fatigue | 8 | 4 |
Pyrexia | 6 | 2 |
Most common AEs leading to discontinuation in patients, % | ||
Increased blood creatinine | 1 | 1 |
Acute renal failure | 1 | 2 |
Supportive-care use during study treatment, % | ||
G-CSF | 46 | 58 |
Epoetin alfa | 18 | 23 |
Darbepoetin alfa | 12 | 26 |
Red blood cell transfusion | 45 | 49 |
Platelet transfusion | 14 | 20 |
. | POM+LoDEX (n = 112) . | POM alone (n = 107) . |
---|---|---|
Hematologic AEs occurring in ≥5% of patients, % | ||
Neutropenia | 41 | 48 |
Anemia | 22 | 24 |
Thrombocytopenia | 19 | 22 |
Leukopenia | 10 | 7 |
Lymphopenia | 7 | 2 |
Febrile neutropenia | 3 | 5 |
Nonhematologic AEs occurring in ≥5% of patients, % | ||
Pneumonia | 22 | 15 |
Fatigue | 14 | 11 |
Dyspnea | 13 | 8 |
Back pain | 10 | 14 |
Urinary tract infection | 9 | 2 |
Sepsis | 5 | 6 |
Dehydration | 5 | 5 |
Acute renal failure | 5 | 8 |
Muscular weakness | 4 | 6 |
Blood creatinine increase | 3 | 6 |
Confusional state | 3 | 7 |
Hypercalcemia | 1 | 10 |
AEs leading to dose reduction in ≥5% of patients, % | ||
Thrombocytopenia | 5 | 9 |
Neutropenia | 4 | 7 |
AEs leading to dose interruption in ≥5% of patients, % | ||
Neutropenia | 9 | 14 |
Thrombocytopenia | 5 | 11 |
Pneumonia | 18 | 12 |
Upper respiratory tract infection | 5 | 9 |
Fatigue | 8 | 4 |
Pyrexia | 6 | 2 |
Most common AEs leading to discontinuation in patients, % | ||
Increased blood creatinine | 1 | 1 |
Acute renal failure | 1 | 2 |
Supportive-care use during study treatment, % | ||
G-CSF | 46 | 58 |
Epoetin alfa | 18 | 23 |
Darbepoetin alfa | 12 | 26 |
Red blood cell transfusion | 45 | 49 |
Platelet transfusion | 14 | 20 |
Treatment-emergent AEs are defined as any AE occurring or worsening on or after the first treatment of the study medication and within 30 days after treatment-phase end date.