| [18F]FDG | Fluorodeoxyglucose |
| 4E-BP1 | Eukaryotic translation initiation factor 4E-binding protein 1 |
| ABC | Activated B-cell |
| AE | Adverse event |
| ALT | Alanine aminotransferase |
| AR | Androgen receptor |
| AR-V7 | Androgen receptor variant 7 |
| AST | Aspartate aminotransferase |
| AUC | Area under the curve |
| BCL | B-cell lymphoma |
| BICR-PFS | Blinded independent central review of progression-free survival |
| BID | Twice daily |
| BLRM | Bayesian logistic regression model |
| BRCA1 | Breast cancer A1 |
| BAP1 | BRCA1-associated protein-1 |
| BRD4 | Bromodomain-containing protein 4 |
| BTC | Biliary tract cancer |
| BTK | Bruton’s tyrosine kinase |
| CARD11 | Caspase recruitment domain family member 11 |
| CBR | Clinical benefit rate |
| CCL-3 | Chemokine ligand 3 |
| CCL-4 | Chemokine ligand 4 |
| CDK4/6 | Cyclin-dependent kinase 4/6 |
| CI | Confidence interval |
| CLL | Chronic lymphocytic leukemia |
| Cmax | Maximum concentration drug achieves in a specified compartment |
| CNS | Central nervous system |
| CR | Complete response |
| CRPC | Castration-resistant prostate cancer |
| mCRPC | Metastatic castration-resistant prostate cancer |
| CTCL | Cutaneous T-cell lymphoma |
| CYP450 | Cytochromes P450 |
| CXCL | C-X-C motif ligand |
| DCR | Disease control rate |
| DL | Dose level |
| DLBCL | Diffuse large B-cell lymphoma |
| DLT | Dose-limiting toxicities |
| DoR | Duration of response |
| EGFR | Epidermal growth factor receptor |
| ER | Estrogen receptor |
| ERK | Extracellular-signal regulated kinase |
| ESR1 | Estrogen receptor 1 |
| ESCO1 | Establishment of sister chromatid cohesion N-acetyltransferase 1 |
| FANCE | Fanconi anemia, complementation group E |
| FGFR2 | Fibroblast growth factor receptor 2 |
| FL | Follicular lymphoma |
| FEP | Full evaluable population |
| FOXO3 | Forkhead box O3 |
| GATA3 | GATA-binding protein 3 |
| GBC | Germinal center B-cell |
| GSK3ß | Glycogen synthase kinase 3 beta |
| GCIG | Gynecological cancer intergroup |
| HDAC | Histone deacetylases |
| HER2 | Human epidermal growth factor receptor 2 |
| HIF-1α | Hypoxia-inducible factor-1α |
| HNSCC | Head and neck squamous cell carcinoma |
| HPV | Human papilloma virus |
| HR | Hormone receptor |
| HL | Hodgkin’s lymphoma |
| IC50 | Half-maximal inhibitory concentration |
| iwCLL | International workshop on chronic lymphocytic leukemia |
| IHC | Immunohostochemistry |
| IQR | Interquartile range |
| IMRT | Intensity-modulated radiotherapy |
| IV | Intravenous |
| KRAS | Kirsten rat sarcoma |
| LAR | Luminal androgen receptor |
| LASCCHN | Locally advanced squamous cell cancer of the head and neck |
| LDH | Lactate dehydrogenase |
| LKB1 | Liver kinase B1 |
| LL | Lymphocytic leukemia |
| mAb | Monoclonal antibody |
| MAPK | Mitogen-activated protein kinase |
| MBC | Metastatic breast cancer |
| MCL | Mantle cell lymphoma |
| MCL1 | Induced myeloid leukemia cell differentiation protein |
| MDM2 | Mouse double minute 2 homolog |
| MTD | Maximum tolerated dose |
| MR | Major response |
| mRNA | Messenger ribonucleic acid |
| MRR | Major response rate |
| mTOR | Mechanistic target of rapamycin |
| MZL | Marginal zone lymphoma |
| NCI | National Cancer Institute |
| NK | Natural killer |
| MYD | Myeloid differentiation protein |
| NCRNPD | Neither complete response nor progressive disease |
| N.E. | Not estimated |
| NFKBIA | NF-kappaB inhibitor alpha |
| NGS | Next-generation sequencing |
| iNHL | Indolent non-Hodgkin lymphoma |
| NK | Natural Killer cells |
| N.R. | Not reachable |
| MRI | Magnetic resonance imaging |
| NSCLC | Non-small-cell lung cancer |
| OR | Overall response |
| ORR | Overall response rate |
| OS | Overall survival |
| PAM 50 | Prediction analysis of microarray 50 |
| PCNSL | Primary central nervous system lymphoma |
| PAP | Primary analysis population |
| PCWG2 | Prostate Cancer Clinical Trials Working Group |
| PD | Progressive disease |
| PDGFRA | Platelet-derived growth factor receptor alpha |
| PET | Positron emission tomography |
| PI3K | Phosphoinositide 3-kinase |
| PIK3CA | Phosphatidylinosi-tol-4,5- bisphosphate 3-kinase catalytic subunit alpha |
| PPS | Per protocol sets |
| PFS | Progression-free survival |
| PO | Oral |
| PgR | Progesterone receptor |
| PJP | Pneumocystis jirovecii pneumonia |
| PK | Pharmacokinetics |
| PR | Partial response |
| PRP | Platelet rich plasma |
| PRAS40 | Proline rich AKT substrate of 40 kDa |
| PRES | Posterior reversible encephalopathy syndrome |
| pS6 | Ribosomal protein S6 |
| PSA | Prostate-specific antigen |
| PTCL | Peripheral T cell lymphoma |
| PTEN | Phosphatase and tensin homolog |
| QD | Once daily |
| RDE | Recommended dose on expansion |
| RECIST | Response evaluation criteria in solid tumors |
| RB | Retinoblastoma |
| RP2D | Recommended phase 2 dose |
| RPPA | Reverse phase protein array |
| RPS32 | Ribosomal protein small subunit 32 |
| R/R | Relapsed refractory |
| SCNSL | Secondary central nervous system lymphoma |
| SD | Stable disease |
| SETD2 | SET domaincontaining 2, histone lysine methyltransferase |
| SGLT2 | Sodium-glucose cotransporter-2 |
| SLL | Small lymphocytic lymphoma |
| T1/2 | Half-life |
| TEAEs | Treatment emergent adverse events |
| Tmax | Time to reach maximum concentration |
| TNBC | Triple-negative breast cancer |
| TNFAIP3 | TNF alpha induced protein 3 |
| TP53 | Tumor protein 53 |
| TTF | Time-to-treatment failure |
| TTR | Time to response |
| VEGF | Vascular endothelial growth factor |
| VGPR | Very good partial response |
| WT | Wild type |