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Patients (%) reporting adverse events (AEs).
| Type of AEs | No. (% of total n = 14) |
|---|---|
| Any AEs | 1 (7) |
| Serious AE (grade ≥ 3) | 3 (21) |
| AEs leading to discontinuation | 1 (7) |
| AEs leading to dose reduction | 0 (0) |
| Death due to combination therapy | 0 (0) |
| Death due to disease progression | 9 (64) |
