AUTHOR=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 TITLE=Erdafitinib treatment in metastatic urothelial carcinoma: a real-world analysis JOURNAL=Frontiers in Oncology VOLUME=13 YEAR=2023 URL=https://www.frontiersin.org/journals/oncology/articles/10.3389/fonc.2023.1151701 DOI=10.3389/fonc.2023.1151701 ISSN=2234-943X ABSTRACT=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.