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Multicenter Study
. 2026 Mar 15;158(6):1654-1665.
doi: 10.1002/ijc.70203. Epub 2025 Oct 22.

Enfortumab vedotin plus pembrolizumab in treatment-naïve metastatic urothelial carcinoma patients: An Austrian real-world analysis

Affiliations
Multicenter Study

Enfortumab vedotin plus pembrolizumab in treatment-naïve metastatic urothelial carcinoma patients: An Austrian real-world analysis

Dora Niedersuess-Beke et al. Int J Cancer. .

Abstract

Antibody-drug conjugates (ADCs) and immunotherapy have changed the treatment landscape for locally advanced and metastatic urothelial carcinoma (la/mUC). Clinical trials have demonstrated the superiority of enfortumab vedotin (EV) combined with pembrolizumab (P) over chemotherapy. This retrospective, multicentre Austrian registry analysis evaluated the effectiveness and safety of EV + P in treatment-naïve la/mUC patients in a real-world setting. This study included 203 first-line EV + P treated patients from 20 Austrian centres. The majority were male (77.3%), with a median age of 70 years (range, 26-92), while 33.5% were ≥75 years. Comorbidities were common, with 25.1% having a Charlson Comorbidity Index (CCI) ≥ 5, and 46.3% moderate to severe renal impairment. Among 195 evaluable patients, the objective response rate (ORR) was 63.6% (95% CI, 56.6-70.0), including 21.5% complete responses and 42.1% partial responses. Disease control was achieved in 75.4% (95% CI, 68.9-80.9). Median progression-free survival (PFS) and overall survival (OS) were not reached after a median follow-up of 5.8 months. Poor outcomes were associated with ECOG PS >2 (PFS, p = .003; OS, p< .001) and CCI ≥5 (PFS, p = .011; OS, p = .08). EV + P was generally well tolerated; grade ≥3 treatment-related adverse events occurred in 38.4% of patients and immune-related adverse events in 19.2%. Limitations of this study include its retrospective design and short follow-up. These findings support the clinical use of EV + P as first-line treatment for la/mUC, demonstrating substantial effectiveness and manageable toxicity in a large real-world population, including elderly and comorbid patients. Extended follow-up is warranted to determine long-term survival and predictive markers of response.

Keywords: enfortumab vedotin; metastatic urothelial carcinoma; pembrolizumab; real‐world evidence; registry.

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Conflict of interest statement

Dora Niedersuess‐Beke has received speakers and consultant honoraria from MSD and Astellas Pharma GmbH, as well as a research grant from Astellas Pharma GmbH. Johanna Krauter served as speaker and participated in advisory boards for Merck, and served as speaker for Astellas Pharma GmbH. Thomas Bauernhofer has received honoraria for lectures provided by Johnson & Johnson, AstraZeneca, Bayer, BMS, MSD, Novartis, Ipsen, Esai and Astellas Pharma GmbH. Andreas Banner has received honoraria from Astellas Pharma GmbH. Stefan Aufderklamm participated in advisory boards for Astellas Pharma GmbH and has received honoraria for lectures from Astellas Pharma GmbH. Clemens Wiesinger has received financial support for attending meetings from Bayer AG, Ferring GmbH, Janssen‐Cilag Pharma GmbH, AstraZeneca GmbH; he participated in advisory boards from Janssen‐Cilag Pharma GmbH. Simon Peter Gampenrieder received speaker honoraria from MSD, as well as consulting fees from Astellas Pharma GmbH and MSD. Maximillian Pallauf received honoraria for participating in advisory boards from BMS and AstraZeneca, as well as a travel grant from Johnson & Johnson and AstraZeneca. Josef Mühlmann received consultancy honoraria for Astellas Pharma GmbH. Sonia Vallet has received honoraria from Astellas Pharma GmbH and MSD. Shahrokh Shariat has received honoraria as speaker and consultant for Astellas Pharma GmbH and MSD. Harun Fajkovic has received research support from Johnson & Johnson, Bayer, Astellas Pharma GmbH, Takeda, Baxter and Arthrex; he has received consultancy fees from Johnson & Johnson, Astellas Pharma GmbH, IPSEN, MSD and AFS Medical; he was speaker for Johnson & Johnson, Bayer, Astellas Pharma GmbH, MSD and Boston Scientific; he has received honoraria from Johnson & Johnson, Astellas Pharma GmbH, IPSEN, Bayer, MSD and Takeda; and he participated in scientific advisory boards from Johnson & Johnson, Ferring, Astellas Pharma GmbH, IPSEN, Bayer and MSD. Renate Pichler participated in advisory boards from Astellas Pharma GmbH; she has received honoraria for lectures from Astellas Pharma GmbH and research grants from Astellas Pharma GmbH. The remaining authors have no relevant disclosures.

Figures

FIGURE 1
FIGURE 1
Kaplan–Meier plots of median progression‐free survival (PFS) (A) and median overall survival (OS) (B) (N = 203).
FIGURE 2
FIGURE 2
Kaplan–Meier plots of median progression‐free survival (PFS) (A) and median overall survival (OS) (B) according to Charlson comorbidity index (CCI), as well as ECOG status (PFS, C and OS, D) at treatment initiation (N = 203).

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