Evidence map›Paper›PMID 35953604›Full record

ReviewCancer chemotherapy and pharmacology2022

An update on antibody-drug conjugates in urothelial carcinoma: state of the art strategies and what comes next.

Alberto D'Angelo, Robert Chapman, Marianna Sirico, Navid Sobhani, Martina Catalano, Enrico Mini, Giandomenico Roviello

Open access · hybridAbstract readReview
In one paragraph

Review in Cancer chemotherapy and pharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
4.8field-weighted citation impact, top 4% of its field
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

19 citing papers in PubMed, 23 citations in OpenAlex.

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  14. Emerging molecular therapies in the treatment of bladder cancer.Exploration of targeted anti-tumor therapy · 2024
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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

7 authors at 5 institutions in 3 countries.

Alberto D'AngeloDepartment of Biology and Biochemistry, University of Bath, Bath, BA2 7AY, UK. Ada43@bath.ac.uk.ORCID 0000-0001-8417-9172
Robert ChapmanDepartment of Medicine, Princess Alexandra Hospital NHS Foundation Trust, Harlow, CM20 1QX, UK.
Marianna SiricoDepartment of Medical Oncology, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori", Meldola, Italy.
Navid SobhaniSection of Epidemiology and Population Science, Department of Medicine, Baylor College of Medicine, Houston, TX, 77030, USA.
Martina CatalanoSchool of Human Health Sciences, University of Florence, Largo Brambilla 3, 50134, Florence, Italy.
Enrico MiniDepartment of Health Sciences, University of Florence, vialePieraccini, 6, 50139, Florence, Italy.
Giandomenico RovielloDepartment of Health Sciences, University of Florence, vialePieraccini, 6, 50139, Florence, Italy.
University of Florence · ITBaylor College of Medicine · USIstituto Scientifico Romagnolo per lo Studio e la Cura dei Tumori · ITPrincess Alexandra Hospital NHS Trust · GBUniversity of Bath · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In recent years, considerable progress has been made in increasing the knowledge of tumour biology and drug resistance mechanisms in urothelial cancer. Therapeutic strategies have significantly advanced with the introduction of novel approaches such as immune checkpoint inhibitors and Fibroblast Growth Factor Receptor inhibitors. However, despite these novel agents, advanced urothelial cancer is often still progressive in spite of treatment and correlates with a poor prognosis. The introduction of antibody-drug conjugates consisting of a target-specific monoclonal antibody covalently linked to a payload (cytotoxic agent) is a novel and promising therapeutic strategy. In December 2019, the US Food and Drug Administration (FDA) granted accelerated approval to the nectin-4-targeting antibody-drug conjugate, enfortumab vedotin, for the treatment of advanced or metastatic urothelial carcinomas that are refractory to both immune checkpoint inhibitors and platinum-based treatment. Heavily pre-treated urothelial cancer patients reported a significant, 40% response to enfortumab vedotin while other antibody-drug conjugates are currently still under investigation in several clinical trials. We have comprehensively reviewed the available treatment strategies for advanced urothelial carcinoma and outlined the mechanism of action of antibody-drug conjugate agents, their clinical applications, resistance mechanisms and future strategies for urothelial cancer.

Indexed as

Antineoplastic AgentsCarcinoma, Transitional CellImmunoconjugatesUrinary Bladder NeoplasmsHumansImmune Checkpoint InhibitorsAntineoplastic AgentsImmune Checkpoint InhibitorsImmunoconjugatesAntibody–drug conjugateBladderEnfortumab vedotinHER2ImmunotherapyNectin-4Sacituzumab govitecanUrothelial cancer

Identifiers

PMID35953604
PMCPMC9402760
OpenAlexW4291008779

What OpenQuestion holds

Textmetadata
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.