Evidence map›Paper›PMID 36696077›Full record

ReviewCurrent oncology reports2023

Nectin-4: a Tumor Cell Target and Status of Inhibitor Development.

Wafa Bouleftour, Paul Sargos, Nicolas Magne

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current oncology reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
4.8field-weighted citation impact, top 5% 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

8 citing papers in PubMed, 15 citations in OpenAlex.

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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

3 authors at 3 institutions in 2 countries.

Wafa BouleftourDepartment of Medical Oncology, North Hospital, University Hospital of Saint-Etienne, Saint-Etienne, France.ORCID 0000-0002-8485-9386
Paul SargosDepartment of Radiation Oncology, Institut Bergonié, Bordeaux, France.
Nicolas MagneDepartment of Radiation Oncology, Institut Bergonié, Bordeaux, France. n.magne@bordeaux.unicancer.fr.
Centre Hospitalier Universitaire de Saint-Étienne · FRInstitut Bergonié · FRUniversité Claude Bernard Lyon 1 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewThis study aims to gather the current state of the literature about anti-Nectin-4 innovative associations in solid tumors and to investigate underlying resistance mechanisms. RECENT

findingsAntibody-drug conjugate (ADC) targeting Nectin-4 efficacy gained attention and offers a promising association with other antineoplastic drugs especially in urothelial carcinoma. The heterogeneity of Nectin-4 expression across the molecular subtypes was highlighted especially in urothelial cancers. A unique study using preclinical models demonstrated an upregulation of P-gp expression, which may explain the anti-Nectin-4 resistance mechanisms. Further studies are urgently needed to understand anti-Nectin-4 sensitivity and resistance phenomenon. The growing therapeutic associations of enfortumab vedotin offer optimistic opportunities in management and treatment of wide range of solid tumors including rare aggressive malignancies.

Indexed as

Antineoplastic AgentsCarcinoma, Transitional CellImmunoconjugatesUrinary Bladder NeoplasmsCell Adhesion MoleculesHumansAntineoplastic AgentsCell Adhesion MoleculesImmunoconjugatesAntidrug conjugateBiomarkerHeterogeneityMalignanciesNectin-4Targeted therapy

Identifiers

PMID36696077
OpenAlexW4317931232

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.