Evidence map›Paper›PMID 41154422›Full record

ReviewCancers2025

Navigating Therapeutic Landscapes in Urothelial Cancer: From Chemotherapy to Precision Immuno-Oncology.

Takatoshi Somoto, Takanobu Utsumi, Rino Ikeda, Naoki Ishitsuka, Takahide Noro, Yuta Suzuki, Shota Iijima, Yuka Sugizaki, Ryo Oka, Takumi Endo and 2 more

Abstract readReview
In one paragraph

Review in Cancers, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
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

12 authors.

Takatoshi SomotoDepartment of Urology, Toho University Sakura Medical Center, Sakura 285-8741, Japan.
Takanobu UtsumiDepartment of Urology, Toho University Sakura Medical Center, Sakura 285-8741, Japan.ORCID 0000-0002-9423-7361
Rino IkedaDepartment of Urology, Toho University Sakura Medical Center, Sakura 285-8741, Japan.
Naoki IshitsukaDepartment of Urology, Toho University Sakura Medical Center, Sakura 285-8741, Japan.
Takahide NoroDepartment of Urology, Toho University Sakura Medical Center, Sakura 285-8741, Japan.
Yuta SuzukiDepartment of Urology, Toho University Sakura Medical Center, Sakura 285-8741, Japan.
Shota IijimaDepartment of Urology, Toho University Sakura Medical Center, Sakura 285-8741, Japan.
Yuka SugizakiDepartment of Urology, Toho University Sakura Medical Center, Sakura 285-8741, Japan.
Ryo OkaDepartment of Urology, Toho University Sakura Medical Center, Sakura 285-8741, Japan.
Takumi EndoDepartment of Urology, Toho University Sakura Medical Center, Sakura 285-8741, Japan.
Naoto KamiyaDepartment of Urology, Toho University Sakura Medical Center, Sakura 285-8741, Japan.ORCID 0000-0002-4183-2490
Hiroyoshi SuzukiDepartment of Urology, Toho University Sakura Medical Center, Sakura 285-8741, Japan.ORCID 0000-0001-5838-114X

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesThe therapeutic landscape of advanced or metastatic urothelial carcinoma (UC) has shifted from platinum chemotherapy to precision immuno-oncology. Immune checkpoint inhibitors (ICIs)-pembrolizumab, nivolumab, and avelumab-show efficacy across platinum-refractory, maintenance, and adjuvant settings, yet benefit is limited to subsets, underscoring the need for biomarkers. Antibody-drug conjugates (ADCs), notably enfortumab vedotin(EV), and targeted agents such as FGFR inhibitors further expand options. This review synthesizes current evidence and emerging paradigms to guide combinations and sequencing.

methodsWe performed a narrative synthesis of peer-reviewed trials (emphasizing pivotal phase III studies), key translational investigations, and contemporary guidelines on ICIs, ADCs, HER2-directed therapies, FGFR inhibitors, molecular subtyping, and genomic profiling in UC, integrating efficacy signals, biomarker associations, and practical implications for sequencing.

resultsICIs now occupy multiple settings, but heterogeneous benefit highlights the importance of molecularly informed selection. EV alone and with pembrolizumab has produced unprecedented first-line activity, prompting a strategic shift. Molecular subtyping and genomic profiling delineate phenotypes with variable immune responsiveness and targetable vulnerabilities, enabling rational combinations and refined sequencing. Ongoing trials are evaluating next-generation ADCs, HER2-directed approaches, and dual checkpoint blockade to achieve durable, personalized disease control.

conclusionsManagement of locally advanced or metastatic UC is converging on precision immuno-oncology, wherein biomarker-driven selection, molecular subtyping, and thoughtful sequencing of ICIs, ADCs, and targeted agents are central to optimizing outcomes. Active trials and translational advances are expected to refine personalized strategies and embed molecular guidance into routine care.

Indexed as

antibody–drug conjugatesbladder cancerimmune checkpoint inhibitorsmolecular subtypeurothelial carcinoma

Identifiers

PMID41154422
PMCPMC12562355

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.