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Toxicity (TOX) events and clinical outcomes
| Outcome | Arm A: Daratumumab (n=15) |
Arm B: Edicotinib (n=10) |
| TOX | ||
| Patients with any TOX event | 2 (13%) | 2 (20%) |
| Surgery delay | 0 (0%) | 0 (0%) |
| Surgical complications | 0 (0%) | 1 (10%) |
| Grade 3 infusion reactions >6 hours | 0 (0%) | NA |
| Related grade 2 lasting >14 days | 1 (7%)—infection | 1 (10%)—lymphocyte count decrease |
| Related grade 3, not excepted | 1 (7%)—urticaria | 0 (0%) |
| pCR | ||
| pCR empirical estimate N (%) | 0 (0%) | 0 (0%) |
pCR, pathologic complete remission.
