ADC |
Antibody-drug conjugate |
AEs |
Adverse events |
G3 AE |
Grade 3 adverse event |
AKT |
Protein kinase B |
AR |
Androgen receptor |
ASCO-GU |
Genitourinary Cancers Symposium of the American Society of Clinical Oncology |
BC |
Bladder cancer |
NMIBC |
Nonmuscle invasive bladder cancer |
MIBC |
Muscle invasive bladder cancer |
BSC |
Best supportive care |
CPI |
Checkpoint inhibition |
CR |
Complete response |
CT |
Chemotherapy |
D + R/P |
Docetaxel + Ramucirumab/Placebo |
DoR |
Duration of response |
EAU |
European Association of Urology |
ECOG |
Eastern Cooperative Oncology Group |
EGFR |
Epidermal Growth Factor Receptor |
EMA |
European Medicines Agency |
Erd |
Erdafitinib |
ESMO |
European Society for Medical Oncology |
ESMO |
European Society for Medical Oncology |
EV |
Enfortumab vedotin |
FDA |
United States Food and Drug Administration |
FGFR |
Fibroblast growth factor receptor |
FU |
Follow up |
GA |
Genetic alterations |
HER2 |
Human epidermal growth factor receptor 2 |
i.v. |
Intravenously |
IgG |
Immunglobulin G |
ITT |
Intention to treat |
MAPK |
Mitogen-activated protein kinase |
MHC |
Major histocompatibility complex |
mTOR |
Mechanistic Target of Rapamycin |
M-VAC |
Methotrexate, Vinblastine, Adriamycin and Cisplatin |
NA |
Not available |
NR |
Not reached |
ORR |
Objective response rate |
OS |
Overall survival |
PARP |
poly(ADP-ribose) polymerase |
PD |
Progressive disease |
PD-(L)1 |
Programmed cell death (ligand)-1 |
PFS |
Progression free survival |
PR |
Partial response |
PRISMA |
Preferred Reporting Items for Systematic Review and meta-analysis Statement |
PSN |
Peripheral sensory neuropathy |
RAM |
Ramucirumab |
RECIST |
Response evaluation criteria in solid tumors |
RTK |
Receptor tyrosine kinases |
SG |
Sacituzumab govitecan |
SRM |
Selected regimen |
TCGA |
The Cancer Genome Atlas |
TKI |
Tyrosine kinase inhibitor |
(m)UC |
(Metastatic) urothelial carcinoma |
UTI |
Urinary tract infection |
VEGF |
Vascular endothelial growth factor |
WBC |
White blood cell |