| ACTs | Adoptive Cellular Therapies |
| SASS | Strategic Advances in Sarcoma Science |
| TME | Tumor Microenvironment |
| CARs | Chimeric Antigen Receptors |
| MHC | Major Histocompatibility Complex |
| TCRs | T Cell Receptors |
| PC | Peptide-centric |
| Lete-cel | Letetresgene autoleucel |
| IL1RAP | Interleukin-1 Receptor Accessory Protein |
| NK | Natural Killer |
| MDSCs | Myeloid-Derived Suppressor Cells |
| TAAs | Tumor-Associated Antigens |
| TDAs | Tumor Differentiation Antigens |
| TSAs | Tumor-Specific Antigens |
| pHLA | Peptide-Human Leukocyte Antigen |
| NGS | Next-Generation Sequencing |
| AML | Acute Myeloid Leukemia |
| TILs | Tumor-Infiltrating Lymphocytes |
| AI | Artificial Intelligence |
| DL | Deep Learning |
| AIDPATH | Artificial Intelligence-driven, Decentralized Production for Advanced Therapies in the Hospital |
| ECM | Extracellular Matrix |
| TAMs | Tumor-Associated Macrophages |
| ARG1 | Arginase 1 |
| TGF | Transforming Growth Factor (TGF)-β |
| IL | Interleukin-10 |
| IDO | Indoleamine 2,3-dioxygenase |
| TMB | Tumor Mutation Burden |
| SMRP | Soluble Mesothelin-Related Peptides |
| MPF | Megakaryocytic Potentiating Factor |
| ctDNA | Circulating Tumor DNA |