| 1L | First line |
| 2L | Second line |
| BOR | Best overall response |
| CI | Confidence interval |
| CONSORT | Consolidated Standards of Reporting Trials |
| CR | Complete response |
| D | Docetaxel |
| DCR | Disease control rate |
| DoR | Duration of response |
| ECOG | Eastern Cooperative Oncology Group |
| EORTC | European Organization for Research and Treatment of Cancer |
| G | Gemcitabine |
| HR | Hazard ratio |
| IHC | Immunohistochemistry |
| IRR | Infusion-related reaction |
| ITT | Intention to treat |
| IV | Intravenous |
| KM | Kaplan–Meier |
| LMS | Leiomyosarcoma |
| mBPI-sf | Modified Brief Pain Inventory-short form |
| NONMEM | Nonlinear Mixed Effects Modelling software |
| O | Olaratumab |
| ORR | Objective response rate |
| OS | Overall survival |
| PBO | Placebo |
| PDGF | Platelet-derived growth factor |
| PDGFR | Platelet-derived growth factor receptor |
| PFS | Progression-free survival |
| PK | Pharmacokinetics |
| PR | Partial response |
| PROs | Patient-reported outcomes |
| PS | Performance status |
| QLQ-C30 | Quality of life questionnaire |
| RECIST | Response Evaluation Criteria in Solid Tumors |
| SAE | Serious adverse event |
| SD | Stable disease |
| STS | Soft tissue sarcoma |
| TEAE | Treatment-emergent adverse event |