TY - JOUR
T1 - Erdafitinib treatment in metastatic urothelial carcinoma
T2 - a real-world analysis
AU - Rouvinov, Keren
AU - Levanon, Eran
AU - Peer, Avivit
AU - Sarfaty, Michal
AU - Sarid, David
AU - Neiman, Victoria
AU - Grikshtas, Eduard
AU - Rosenbaum, Eli
AU - Kushnir, Igal
AU - Talmor, Barak
AU - Friger, Michael
AU - Zarbiv, Yonaton
AU - Gez, Eli
AU - Dresler, Hadas
AU - Shalata, Walid
AU - Meirovitz, Amichay
AU - Shrem, Noa Shani
AU - Yakobson, Alexander
AU - Mermershtain, Wilmosh
AU - Keizman, Daniel
N1 - Publisher Copyright:
Copyright © 2023 Rouvinov, Levanon, Peer, Sarfaty, Sarid, Neiman, Grikshtas, Rosenbaum, Kushnir, Talmor, Friger, Zarbiv, Gez, Dresler, Shalata, Meirovitz, Shrem, Yakobson, Mermershtain and Keizman.
PY - 2023/1/1
Y1 - 2023/1/1
N2 - 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.
AB - 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.
KW - erdafitinib
KW - fibroblast growth factor receptor (FGFR) inhibitor
KW - metastatic urothelial carcinoma
KW - real-world analysis
KW - treatment
UR - http://www.scopus.com/inward/record.url?scp=85161352262&partnerID=8YFLogxK
U2 - 10.3389/fonc.2023.1151701
DO - 10.3389/fonc.2023.1151701
M3 - Article
C2 - 37293597
AN - SCOPUS:85161352262
SN - 2234-943X
VL - 13
JO - Frontiers in Oncology
JF - Frontiers in Oncology
M1 - 1151701
ER -