| ADC | antibody–drug conjugate |
| AGO | Arbeitsgemeinschaft Gynäkologische Onkologie |
| ASCO | American Society of Clinical Oncology |
| BOR | best overall response |
| CHMP | Committee for Medicinal Products for Human Use |
| ChT | chemotherapy |
| CrCl | creatinine clearance |
| DAR | drug-to-antibody ratio |
| Dato-DXd | datopotamab deruxtecan |
| DCR | disease control rate |
| DOR | duration of response |
| DXd | deruxtecan payload |
| ESMO | European Society for Medical Oncology |
| EU | European Union |
| FDA | U.S. Food and Drug Administration |
| G-CSF | granulocyte colony-stimulating factor |
| GR | grade of recommendation |
| HER2 | human epidermal growth factor receptor 2 |
| HR | hormone receptor; hazard ratio |
| HR+/HER2− | hormone receptor-positive/HER2-negative |
| ILD | interstitial lung disease |
| LoE | level of evidence |
| MCBS | Magnitude of Clinical Benefit Scale |
| NCCN | National Comprehensive Cancer Network |
| ORR | objective response rate |
| OS | overall survival |
| PD | progressive disease |
| PD-1 | programmed cell death protein 1 |
| PD-L1 | programmed death-ligand 1 |
| PFS | progression-free survival |
| pp | percentage points |
| SG | sacituzumab govitecan |
| SN-38 | active metabolite of irinotecan |
| T-DXd | trastuzumab deruxtecan |
| TNBC | triple-negative breast cancer |
| TOP1 | topoisomerase I |
| TROP2 | trophoblast cell-surface antigen 2 |
| TTR | time to response |
| UGT1A1 | uridine diphosphate glucuronosyltransferase 1A1 |