C-Reactive Protein Is a Potential Prognostic Marker in Patient with Advanced or Metastatic Urothelial Carcinoma Treated with Enfortumab Vedotin: A Multi-Center Retrospective Study

Author:

Morikawa Toshiharu1ORCID,Naiki Taku12ORCID,Sugiyama Yosuke3ORCID,Naiki-Ito Aya4ORCID,Nagai Takashi1ORCID,Etani Toshiki1,Iida Keitaro1,Isobe Teruki1,Noda Yusuke15,Shimizu Nobuhiko1ORCID,Aoki Maria12,Gonda Masakazu1,Banno Rika6,Kubota Hiroki7,Ando Ryosuke1,Umemoto Yukihiro12,Kawai Noriyasu1ORCID,Yasui Takahiro1ORCID

Affiliation:

1. Department of Nephro-Urology, Graduate School of Medical Sciences, Nagoya City University, Nagoya 467-8601, Japan

2. Department of Urology, Nagoya City University West Medical Center, Nagoya 467-8601, Japan

3. Department of Pharmacy, Nagoya City University Hospital, Nagoya 467-8601, Japan

4. Department of Experimental Pathology and Tumor Biology, Graduate School of Medical Sciences, Nagoya City University, Nagoya 467-8601, Japan

5. Department of Urology, Anjo Kosei Hospital, Anjo 446-8602, Japan

6. Department of Urology, Konan Hospital, Konan 483-8704, Japan

7. Department of Urology, Kainan Hospital, Yatomi 498-8502, Japan

Abstract

Background: In the EV-301 trial, enfortumab vedotin prolonged survival in patients with locally advanced or metastatic urothelial carcinoma previously treated with platinum-based therapy and programmed cell death 1/programmed death-ligand 1 inhibitor. However, real-world Asian data are limited, and potential prognostic markers are non-existent. We aimed to investigate potential prognostic markers for enfortumab vedotin therapy in Asian patients. Methods: We retrospectively enrolled 61 Japanese patients treated with enfortumab vedotin therapy at our hospital and affiliated hospitals between January 2019 and September 2023. Results: Enrolled patients (38 men, 23 women; median age 74 [IQR: 68–79] years) had bladder cancer (26 patients) or upper-tract urothelial carcinoma (35 patients). Fifty-four patients reported adverse events (grade >3 in 12). Skin disorders, pruritus, and neuropathy were common adverse effects. The median overall survival was 17.1 months (95% confidence interval: 10.0–not applicable). In multivariate analysis, the C-reactive protein level was an independent marker predicting favorable overall survival with enfortumab vedotin. Patient characteristics did not differ between C-reactive protein-high and -low groups. Conclusions: Our study provides real-world data showing that enfortumab vedotin prolonged survival in Asian patients similar to the EV-301 trial. Additionally, the C-reactive protein level might be considered a prognostic marker of enfortumab vedotin therapy in such patients.

Publisher

MDPI AG

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