Real-world effectiveness of avelumab, pembrolizumab, and enfortumab vedotin in patients with advanced urothelial carcinoma with squamous differentiation (ARON-2EV)
Year: 2026
Type: article
Study design: Observational Study
Abstract: INTRODUCTION: Avelumab, pembrolizumab, and enfortumab vedotin (EV) demonstrated efficacy in mUC following platinum-based chemotherapy. However, real-world data in patients with urothelial carcinoma with squamous differentiation (UCSD) are limited. The aim of this study is to assess the real-world clinical outcomes of avelumab, pembrolizumab, or EV in mUCSD patients. MATERIALS AND METHODS: The ARON-2EV study is a retrospective, international, multicenter analysis in patients with mUC treated with avelumab, pembrolizumab, or EV across 79 centers in 21 countries. Patients were divided into three cohorts: 1 (avelumab), 2 (pembrolizumab), and 3 (EV). Primary endpoints were overall survival (OS) and time on treatment (ToT). Secondary objectives included evaluating clinical factors associated with outcomes and exploring the impact of UCSD histology on response to therapy. Statistical methods included Kaplan-Meier estimates, log-rank tests, Fisher's exact and chi-square tests, and Pearson's correlation coefficients. RESULTS: A total of 1918 patients, 1696 with advanced pure UC (pUC) and 222 with mUCSD (36 in cohort 1, 111 in cohort 2, and 75 in cohort 3), were included. Median OS was shorter in patients with UCSD compared to patients with pUC histology in the three cohorts (1: 13.0 vs 26.8 months, HR 2.66, p = 0.003; 2: 10.2 vs 18.5 months, HR 1.52, p = 0.008; and 3: 7.6 vs 13.1 months, HR 1.68, p = 0.011). Median ToT was shorter in patients with UCSD compared to patients with pUC histology in cohort 1 (3.5 vs 5.6 months, HR 1.57, p = 0.044) and 3 (7.6 vs 13.6 months, HR 1.83, p = 0.005) but not in cohort 2 (3.7 vs 4.7 months, HR 1.19, p = 0.177). Response to therapy was negatively correlated with UCSD histology in cohorts 2 (correlation coefficient 0.094, p = 0.008) and 3 (correlation coefficient 0.107, p = 0.021), while response to avelumab was not correlated with UCSD (correlation coefficient 0.072, p = 0.263). CONCLUSIONS: UCSD is a histology with a poor prognosis and response to treatments compared to pUC. Treatments activity and effectiveness in divergent differentiations should be addressed in dedicated prospective studies. TRIAL REGISTRATION NUMBER: NCT05290038.
Source: Cancer Immunology Immunotherapy
Authors: Veronica Mollica, Francesco Massari, Kazutoshi Fujita, Patrizia Giannatempo, Enrique Grande, Thomas Büttner, Maria T. Bourlon, Tarek Taha, Wataru Fukuokaya, Zin W. Myint, Renate Pichler, Kirstin Binz, Javier Molina‑Cerrillo, Jindrich Kopecky, Alfonso Gómez de Liaño, Jakub Kucharz, Ondřej Fiala, Marc R. Matrana, Ray Manneh Kopp, Mattia Alberto Di Civita, Anca Zgura, Jawaher Ansari, Randi Kihnel, Francesca De Felice, Martín Angel, Fernando Sabino M. Monteiro, Andrey Soares, Yuksel Urun, Sebastiano Buti, Daniele Santini, Matteo Santoni
Institutions: IRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola, University of Bologna, Kindai University, Fondazione IRCCS Istituto Nazionale dei Tumori, MD Anderson Cancer Center Madrid, University Hospital Bonn, Instituto Nacional de Ciencias Médicas y Nutrición Salvador Zubirán, Universidad Panamericana, Royal Marsden NHS Foundation Trust, Jikei University School of Medicine, University of Kentucky, Markey Cancer Center, Innsbruck Medical University, Universität Innsbruck, University of Kansas, The University of Kansas Cancer Center, Hospital Universitario Ramón y Cajal, University Hospital Hradec Králové, The Maria Sklodowska-Curie National Research Institute of Oncology, Charles University, Ochsner Medical Center, Policlinico Umberto I, Carol Davila University of Medicine and Pharmacy, Institutul Oncologic Bucuresti, Tawam Hospital, Sapienza University of Rome, Instituto Alexander Fleming, Hospital Sírio-Libanês, Latin American Cooperative Oncology Group (LACOG), Hospital Israelita Albert Einstein, Ankara University, University of Parma, Ospedale di Macerata
Language: English
Subfield: Surgery
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $4,590
Funder: Università di Bologna
OpenAlex ID: W7140227002
