| AE | Adverse Events |
| ALB | Albumin |
| ALT | Alanine Aminotransferase |
| AST | Aspartate Aminotransferase |
| CapTem | Capecitabine and Temozolomide |
| CI | Confidence Interval |
| CR | Complete Response |
| CT | Computed Tomography |
| CTCAE | Common Terminology Criteria for Adverse Events |
| DCR | Disease Control Rate |
| ECOG PS | Eastern Cooperative Oncology Group Performance Status |
| GBq | Gigabecquerel |
| Gy | Gray |
| HCC | Hepatocellular Carcinoma |
| HPFS | Hepatic Progression-Free Survival |
| HR | Hazard Ratio |
| IQR | Interquartile Range |
| mRECIST | Modified Response Evaluation Criteria in Solid Tumors |
| NELM | Neuroendocrine Liver Metastases |
| NET | Neuroendocrine Tumor |
| NR | Not Reported/Not Reached |
| ORR | Objective Response Rate |
| OS | Overall Survival |
| PD | Progressive Disease |
| PFS | Progression-Free Survival |
| PET/CT | Positron Emission Tomography/CT |
| PR | Partial Response |
| PRISMA | Preferred Reporting Items for Systematic Reviews and Meta-Analyses |
| ROBINS-I | Risk Of Bias In Non-randomized Studies of Interventions |
| SD | Stable Disease |
| SI | Symptom Improvement |
| SIRT | Selective Internal Radiation Therapy |
| SPECT/CT | Single-Photon Emission Computed Tomography/CT |
| SSA | Somatostatin Analog |
| SUVmax | Maximum Standardized Uptake Value |
| TACE | Transarterial Chemoembolization |
| TAE | Transarterial Embolization |
| TARE | Transarterial Radioembolization |
| WMO | Dutch Medical Research Involving Human Subjects Act |
| WHO | World Health Organization |
| Y-90 | Yttrium-90 |