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Erdafitinib treatment in metastatic urothelial carcinoma: a real-world analysis

BACKGROUND: Erdafitinib, a fibroblast growth factor receptor (FGFR) inhibitor is a standard post chemotherapy advanced treatment line for metastatic urothelial carcinoma harboring FGFR2/3 genomic alterations. It was approved based on a phase 2 clinical trial, revealing a 40% response rate, and 13.8...

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Detalles Bibliográficos
Autores principales: Rouvinov, Keren, Levanon, Eran, Peer, Avivit, Sarfaty, Michal, Sarid, David, Neiman, Victoria, Grikshtas, Eduard, Rosenbaum, Eli, Kushnir, Igal, Talmor, Barak, Friger, Michael, Zarbiv, Yonaton, Gez, Eli, Dresler, Hadas, Shalata, Walid, Meirovitz, Amichay, Shrem, Noa Shani, Yakobson, Alexander, Mermershtain, Wilmosh, Keizman, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10244774/
https://www.ncbi.nlm.nih.gov/pubmed/37293597
http://dx.doi.org/10.3389/fonc.2023.1151701
Descripción
Sumario:BACKGROUND: Erdafitinib, a fibroblast growth factor receptor (FGFR) inhibitor is a standard post chemotherapy advanced treatment line for metastatic urothelial carcinoma harboring FGFR2/3 genomic alterations. It was approved based on a phase 2 clinical trial, revealing a 40% response rate, and 13.8 months overall survival. These FGFR genomic alterations are uncommon. Thus, real-world data on erdafitinb use is scant. We herein describe erdafitinib treatment outcome in a real world patient cohort. METHODS: We retrospectively reviewed the data of patients treated with erdafitinib from 9 Israeli medical centers. RESULTS: Twenty-five patients with metastatic urothelial carcinoma (median age 73, 64% male, 80% with visceral metastases) were treated with erdafitinib between January 2020 to October 2022. A clinical benefit (complete response 12%, partial response 32%, stable disease 12%) was seen in 56%. Median progression-free survival was 2.7 months, and median overall survival 6.73 months. Treatment related toxicity ≥ grade 3 occurred in 52%, and 32% discontinued therapy due to adverse events. CONCLUSIONS: Erdafitinib therapy is associated with a clinical benefit in the real world setting, and associated with similar toxicity as reported in prospective clinical trials.