Evidence map›Paper›PMID 42407197›Full record

ArticleESMO open2026

Real-world prognostic assessment of the HERO score in metastatic urothelial carcinoma treated with enfortumab vedotin (ARON-2EV study).

G Roviello, F Ciccimarra, F Urabe, B Melichar, H Studentova, D Niedersuess-Beke, A Mota, T Büttner, A Gómez de Liaño, A Yano and 15 more

Abstract readMulticenter Study
In one paragraph

Article in ESMO open, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

25 authors.

G RovielloDepartment of Health Sciences, Section of Clinical Pharmacology and Oncology, University of Florence, Florence, Italy. Electronic address: giandomenico.roviello@unifi.it.
F CiccimarraS.S.D. C.O.r.O. Bed Management Presa in Carico, TDM, IRCCS Istituto Tumori "Giovanni Paolo II", Bari, Italy.
F UrabeDepartment of Urology, The Jikei University School of Medicine, Tokyo, Japan.
B MelicharDepartment of Oncology, Faculty of Medicine and Dentistry, Palacký University, Olomouc, Czech Republic.
H StudentovaDepartment of Oncology, Faculty of Medicine and Dentistry, Palacký University, Olomouc, Czech Republic.
D Niedersuess-BekeDepartment of Internal Medicine I, Centre for Oncology and Haematology, Vienna Healthcare Group, Ottakring, Vienna, Austria.
A MotaClínica Assistência Multidisciplinar em Oncologia, Salvador, Brazil.
T BüttnerDepartment of Urology, University Hospital Bonn, Bonn, Germany.
A Gómez de LiañoMedical Oncology Department, CHU Insular-Materno Infantil, Las Palmas, Spain.
A YanoDepartment of Urology, Saitama Medical Center, Saitama Medical University, Kawagoe, Saitama, Japan.
Z W MyintDivision of Medical Oncology, Department of Internal Medicine, Markey Cancer Center, University of Kentucky, Lexington, USA.
R M KoppClinical Oncology, Sociedad de Oncología y Hematología del Cesar, Valledupar, Colombia.
A ZguraDepartment of Obstetrics-Radiotherapy, Alexandru Trestioreanu Institute of Oncology, "Carol Davila" University of Medicine and Pharmacy, Bucharest, Romania.
A PintoDepartment of Medical Oncology, Hospital Universitario La Paz, Madrid, Spain.
M AngelInstituto Alexander Fleming, Ciudad De Buenos Aires, Argentina.
D TuralDepartment of Medical Oncology, Koç University School of Medicine, Istanbul, Turkey.
R KanesvaranDivision of Medical Oncology, National Cancer Centre Singapore, Singapore, Singapore.
Y ÜrünDepartment of Medical Oncology, Faculty of Medicine, Ankara University, Ankara, Turkey.
J Molina-CerrilloDepartment of Medical Oncology, Hospital Ramón y Cajal, Madrid, Spain; ARON Research Foundation ETS, Macerata, Italy.
F S Marques MonteiroARON Research Foundation ETS, Macerata, Italy; Oncology and Hematology Department, Hospital Sírio Libanês, Brasília, Brazil; Latin American Cooperative Oncology Group-LACOG, Porto Alegre, Brazil.
F MassariARON Research Foundation ETS, Macerata, Italy; Medical Oncology, IRCCS Azienda Ospedaliero-Universitaria Di Bologna, Bologna, Italy; Department of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy.
O FialaARON Research Foundation ETS, Macerata, Italy; Department of Oncology and Radiotherapeutics, Faculty of Medicine and University Hospital in Pilsen, Charles University, Pilsen, Czech Republic; Biomedical Center, Faculty of Medicine in Pilsen, Charles University, Pilsen, Czech Republic.
M SantoniARON Research Foundation ETS, Macerata, Italy; Oncology Unit, Macerata Hospital, Macerata, Italy.
L AntonuzzoCareggi University Hospital, Oncology Unit, Florence, Italy; Department of Experimental and Clinical Medicine, University of Florence, Florence, Italy.
A RizzoS.S.D. C.O.r.O. Bed Management Presa in Carico, TDM, IRCCS Istituto Tumori "Giovanni Paolo II", Bari, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEnfortumab vedotin (EV) is a standard treatment for metastatic urothelial carcinoma (mUC) after platinum-based chemotherapy and immune checkpoint inhibitors. However, reliable and clinically accessible prognostic tools for patients treated with EV remain limited. We evaluated the clinical prognostic performance of the HERO score in a large real-world cohort of EV-treated patients. PATIENTS AND

methodsARON-2EV is a retrospective multicenter cohort study including patients with mUC treated with EV after platinum-based chemotherapy and immune checkpoint inhibitors. The association between the HERO score, based on hemoglobin level and neutrophil-to-lymphocyte ratio, and survival outcomes (overall survival and progression-free survival) was assessed. Response analyses were considered exploratory.

resultsA total of 548 patients with mUC treated with EV were included in the analysis. Median overall survival was 12.4 months and median progression-free survival was 6.8 months. The HERO score was associated with survival and response outcomes, with patients with a score of 2 experiencing the most favorable outcomes. These associations remained consistent across multivariable analyses.

conclusionsIn this large international real-world cohort, the HERO score was associated with survival and response outcomes in patients with mUC treated with EV, particularly through identification of a subgroup with a more favorable prognosis (score 2). However, discrimination between lower score categories was less pronounced. Further prospective refinement and evaluation of the HERO score are warranted, particularly in contemporary EV-based treatment strategies.

Indexed as

Antibodies, MonoclonalCarcinoma, Transitional CellUrologic NeoplasmsAgedAged, 80 and overFemaleHumansMalePrognosisProgression-Free SurvivalRetrospective StudiesAntibodies, Monoclonalenfortumab vedotinenfortumab vedotinHERO scoreprognostic factorsreal-world studyurothelial carcinoma

Identifiers

PMID42407197
PMCPMC13355806

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.