Table 3.
Treatment-emergent adverse events occurring in ≥15% of patients
High-risk nmCRPC (n = 51) | ||
---|---|---|
All grades | Grade ≥3* | |
No. of patients with ≥1 TEAE | 51 (100) | 21 (41) |
No. of patients with a serious TEAE | 16 (31) | 12 (24) |
TEAEs, n (%) | All grades | Grade ≥3* |
Fatigue | 31 (61) | 2 (4) |
Diarrhea | 22 (43) | 1 (2) |
Nausea | 20 (39) | 0 |
Arthralgia | 11 (22) | 1 (2) |
Back pain | 11 (22) | 0 |
Dysgeusia | 11 (22) | 0 |
Hypothyroidism | 11 (22) | 0 |
Hot flush | 10 (20) | 0 |
Pain in extremity | 10 (20) | 1 (2) |
Cough | 10 (20) | 0 |
Abdominal pain | 9 (18) | 0 |
Decreased weight | 9 (18) | 0 |
Pollakiuria | 9 (18) | 0 |
Constipation | 8 (16) | 0 |
Nasopharyngitis | 8 (16) | 0 |
Hematuria | 8 (16) | 0 |
Upper respiratory infection | 8 (16) | 0 |
nmCRPC = nonmetastatic castration-resistant prostate cancer; TEAE = treatment-emergent adverse event.
Listed grade ≥3 adverse events are those with an overall incidence ≥15%.