| 131I | Iodine-131 |
| 177Lu | Lutetium-177 |
| AE(s) | Adverse event(s) |
| AXL | AXL receptor tyrosine kinase |
| bid | Twice daily |
| CVD | Cyclophosphamide–Vincristine–Dacarbazine |
| D1, D1–5 | Day 1; Days 1 through 5 |
| DOTATATE | DOTA-Tyr3-octreotate (Lu-177 DOTATATE) |
| FLR/FLT3 | Fms-like tyrosine kinase 3 (FLT3) |
| GI | Gastrointestinal |
| GEP-NET | Gastroenteropancreatic neuroendocrine tumor |
| HFS | Hand-foot syndrome |
| HIF-2α | Hypoxia-inducible factor 2 alpha |
| HR | Hazard ratio |
| HTN | Hypertension |
| IM | Intramuscular |
| IRB | Institutional Review Board |
| KIT | KIT proto-oncogene receptor tyrosine kinase (CD117) |
| LAR | Long-acting release (e.g., octreotide LAR) |
| mg/m2 | Milligrams per square meter |
| MGMT | O6-methylguanine-DNA methyltransferase |
| MIBG | Meta-iodobenzylguanidine |
| mo | Months |
| MET | MET proto-oncogene receptor tyrosine kinase |
| NET | Neuroendocrine tumor |
| NIH | National Institutes of Health |
| ORR | Objective response rate |
| OS | Overall survival |
| PDGFR | Platelet-derived growth factor receptor |
| PFS | Progression-free survival |
| PO | By mouth (per os) |
| PPGL | Pheochromocytoma and Paraganglioma |
| PR | Partial response |
| PRRT | Peptide receptor radionuclide therapy |
| qd | Once daily |
| q21–28d/q28d | Every 21–28 days/every 28 days |
| RET | RET proto-oncogene receptor tyrosine kinase |
| SC | Subcutaneous |
| SD | Stable disease |
| SDHB | Succinate dehydrogenase complex iron sulfur subunit B |
| SI-NET | Small-intestinal neuroendocrine tumor |
| SSTR | Somatostatin receptor |
| SSA | Somatostatin analog |
| TKI | Tyrosine kinase inhibitor |
| TMZ | Temozolomide |
| TTP | Time to progression |
| VEGFR | Vascular endothelial growth factor receptor |
| α/β-blockade | Alpha/Beta-adrenergic blockade |