| Literature DB >> 35962938 |
Jenny Peng1, Srikala Sridhar1, Arlene Odelia Siefker-Radtke2, Shamini Selvarajah3,4, Di Maria Jiang5.
Abstract
OPINION STATEMENT: As we come to better understand cancer genomics, we are increasingly shifting towards precision medicine. FGFR has been elucidated as one of the oncogenic driver pathways in urothelial carcinoma, leading to exciting targeted drug development. Although many agents are being investigated, erdafitinib is the only FGFR inhibitor currently approved by the FDA for treating platinum-refractory metastatic urothelial carcinoma harboring susceptible FGFR2/3 alterations, with seemingly higher response rates than second-line chemotherapy or immunotherapy. In this review, we summarize the clinical data supporting FGFR inhibition, ways to optimize its use in routine clinical practice including FGFR testing, dosing, and toxicity management. We also highlight ongoing efforts evaluating combination strategies and testing in earlier treatment settings to further expand this targeted therapeutic approach in urothelial carcinoma.Entities:
Keywords: Bladder cancer; Clinical trial; Erdafitinib; FGFR; Targeted therapy; Urothelial cancer
Mesh:
Substances:
Year: 2022 PMID: 35962938 DOI: 10.1007/s11864-022-01009-4
Source DB: PubMed Journal: Curr Treat Options Oncol ISSN: 1534-6277