Evidence map›Paper›PMID 42485700›Full record

ArticleESMO open2026

Comparative efficacy of perioperative systemic therapies for muscle-invasive bladder cancer: a network meta-analysis of randomized trials.

B A Maiorano, M Maruzzo, A Ślusarczyk, J D Subiela, F Soria, S Albisinni, A Mari, F Claps, R Contieri, A Gallioli and 18 more

Abstract readNetwork Meta-AnalysisComparative 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

28 authors.

B A MaioranoDepartment of Medical Oncology, Comprehensive Cancer Center, IRCCS San Raffaele, Milan, Italy. Electronic address: maiorano.brigida@hsr.it.
M MaruzzoOncology Unit 3, Istituto Oncologico Veneto IOV - IRCCS, Padova, Italy.
A ŚlusarczykDepartment of General, Oncological and Functional Urology, Medical University of Warsaw, Warsaw, Poland.
J D SubielaDepartment of Urology, Hospital Universitario Ramón y Cajal, IRYCIS, Universidad de Alcalá, Madrid, Spain.
F SoriaDivision of Urology, Department of Surgical Sciences, AOU Città della Salute e della Scienza di Torino, Torino School of Medicine, Torino, Italy.
S AlbisinniUrology Unit, Department of Surgical Sciences, Università Tor Vergata, Rome, Italy.
A MariUnit of Oncologic Minimally-Invasive Urology and Andrology, Department of Experimental and Clinical Medicine, Careggi Hospital, University of Florence, Florence, Italy.
F ClapsOncological Urology, Veneto Institute of Oncology IRCCS, Padua, Italy.
R ContieriDepartment of Urology, National Cancer Institute, IRCCS Fondazione G. Pascale, Naples, Italy.
A GallioliDepartment of Urology, Fundació Puigvert, Barcelona, Spain; Institut de Recerca Sant Pau (IR SANT PAU), Barcelona, Spain.
J Caño-VelascoDepartment of Urology, Clinica Universidad de Navarra, Cancer Center, Pamplona, Spain.
D D'AndreaDepartment of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
E LaukhtinaDepartment of Urology, Comprehensive Cancer Center, Medical University of Vienna, Vienna, Austria.
G MarcqUrology Department, Claude Huriez Hospital, CHU Lille, Lille, France.
W KrajewskiDepartment of Minimally Invasive Robotic Urology, Center of Excellence in Urology, Wroclaw Medical University, Wrocław, Poland.
E Grobet-JeandinDepartment of Urology, Geneva University Hospitals (HUG), University of Geneva, Geneva, Switzerland.
L AfferiDepartment of Urology, Luzerner Kantonsspital, Lucerne, Switzerland.
F Del GiudiceDepartment of Maternal Infant and Urologic Sciences, "Sapienza" University of Rome, Policlinico Umberto I Hospital, Rome, Italy.
A RizzoSSD COrO Bed Management Presa in Carico, TDM, IRCCS Istituto Tumori "Giovanni Paolo II", Bari, Italy.
M MoschiniDivision of Experimental Oncology, Department of Urology, Urological Research Institute, Vita-Salute San Raffaele University, Milan, Italy.
L S MertensDepartment of Urology, Netherlands Cancer Institute, Amsterdam, The Netherlands.
A CigliolaDepartment of Medical Oncology, Comprehensive Cancer Center, IRCCS San Raffaele, Milan, Italy.
C MercinelliDepartment of Medical Oncology, Comprehensive Cancer Center, IRCCS San Raffaele, Milan, Italy.
M PiacentiniDepartment of Medical Oncology, Comprehensive Cancer Center, IRCCS San Raffaele, Milan, Italy.
M SantoniMedical Oncology Unit, Macerata Hospital, Macerata, Italy.
B PradèreDepartment of Urology UROSUD, La Croix du Sud Hospital, Quint-Fonsegrives, France.
A NecchiDepartment of Medical Oncology, Comprehensive Cancer Center, IRCCS San Raffaele, Milan, Italy; Vita-Salute San Raffaele University, Milan, Italy.
Young Academic Urologist (YAU) Urothelial Carcinoma Working Group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe perioperative treatment landscape of muscle-invasive bladder cancer (MIBC) is rapidly evolving with the introduction of immune checkpoint inhibitor (ICI)- and antibody-drug conjugate (ADC)-based strategies. However, direct randomized comparisons among contemporary regimens are lacking, limiting the interpretation and positioning of treatments. We aimed to compare the efficacy of perioperative systemic treatment strategies for MIBC with a network meta-analysis (NMA) of randomized controlled trials (RCTs). PATIENTS AND

methodsPubMed, Embase, Web of Science, and congress abstracts were systematically searched up to 28 February 2026. Phase II-III RCTs enrolling patients with MIBC treated with perioperative systemic therapy initiated before radical cystectomy and reporting overall survival (OS), event-free survival (EFS), and/or pathological complete response (pCR) were included. A frequentist graph-theoretical NMA was carried out to compare three contemporary RCTs using a star-shaped network anchored to gemcitabine-cisplatin (GC) as the common comparator. Treatment ranking was estimated using P-scores. The primary outcome was OS. Secondary outcomes included EFS and pCR.

resultsIn total, 2293 patients from three RCTs contributed to the primary network. Compared with GC, enfortumab vedotin-pembrolizumab (EVP) was associated with improved OS [hazard ratio (HR) 0.65], as was GC plus durvalumab (HR 0.75). EVP and GC plus durvalumab were also associated with improved EFS (EVP HR 0.53, GC plus durvalumab HR 0.68) and higher pCR rates [EVP odds ratio (OR) 2.62, GC plus durvalumab OR 1.57] compared with GC. Across evaluated endpoints, EVP consistently achieved the most relevant P-score-based ranking. Subgroup-specific and sensitivity analyses demonstrated a consistent treatment direction.

conclusionsIn this NMA of RCTs, perioperative regimens incorporating ICIs and ADCs were associated with improved survival and pathologic response outcomes compared with GC alone. Given the sparse star-shaped network and the absence of closed loops, these findings should be interpreted as indirect comparative estimates rather than definitive evidence of treatment superiority, while still providing a clinically relevant framework for contextualizing contemporary perioperative regimens.

Indexed as

Antineoplastic Combined Chemotherapy ProtocolsPerioperative CareUrinary Bladder NeoplasmsAntibodies, Monoclonal, HumanizedCisplatinCystectomyDeoxycytidineGemcitabineHumansRandomized Controlled Trials as TopicTreatment OutcomeAntibodies, Monoclonal, HumanizedCisplatinDeoxycytidineGemcitabinedurvalumabenfortumab vedotinmuscle-invasive bladder cancer (MIBC)pembrolizumabperioperativeradical cystectomy

Identifiers

PMID42485700
PMCPMC13427403

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