Evidence map›Paper›PMID 40838147›Full record

ArticleTherapeutic advances in medical oncology2025

Expression patterns of TROP2 and Nectin-4 in oropharyngeal squamous cell carcinoma in relation to HPV status: potential biomarkers for targeted therapy.

Charlotte Klasen, Hans N C Eckel, Nora Wuerdemann, Joseph Böckelmann, Karl Knipper, Malte Suchan, Kariem Sharaf, Shachi Jenny Sharma, Helen Abing, Arthur Charpentier and 7 more

Abstract read
In one paragraph

Article in Therapeutic advances in medical oncology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

17 authors.

Charlotte KlasenDepartment of Otorhinolaryngology, Head and Neck Surgery, Faculty of Medicine and University Hospital Cologne, Kerpernerstraße 62, Cologne 50923, Germany Center for Molecular Medicine Cologne (CMMC), Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.ORCID https://orcid.org/0009-0009-3120-0439
Hans N C EckelDepartment of Otorhinolaryngology, Head and Neck Surgery, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.ORCID https://orcid.org/0000-0002-6947-9836
Nora WuerdemannCenter for Molecular Medicine Cologne (CMMC), Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
Joseph BöckelmannInstitute of Pathology, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.
Karl KnipperFaculty of Medicine and University Hospital of Cologne, Department of General, Visceral and Cancer Surgery, University of Cologne, Cologne, Germany.
Malte SuchanDepartment of Otorhinolaryngology, Head and Neck Surgery, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.
Kariem SharafDepartment of Otorhinolaryngology, Head and Neck Surgery, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.ORCID https://orcid.org/0000-0001-7799-4005
Shachi Jenny SharmaDepartment of Otorhinolaryngology, Head and Neck Surgery, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.
Helen AbingDepartment of Otorhinolaryngology, Head and Neck Surgery, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.
Arthur CharpentierDepartment of Otorhinolaryngology, Head and Neck Surgery, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.
Julia EsserDepartment of Otorhinolaryngology, Head and Neck Surgery, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.
Kevin HansenDepartment of Otorhinolaryngology, Head and Neck Surgery, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.
Marcel MayerDepartment of Otorhinolaryngology, Head and Neck Surgery, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.ORCID https://orcid.org/0000-0001-9963-1109
Louis JansenDepartment of Otorhinolaryngology, Head and Neck Surgery, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.ORCID https://orcid.org/0000-0003-0332-1099
Jens Peter KlußmannDepartment of Otorhinolaryngology, Head and Neck Surgery, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.
Alexander QuaasInstitute of Pathology, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.
Su Ir LyuInstitute of Pathology, Faculty of Medicine and University Hospital Cologne, Cologne, Germany.ORCID https://orcid.org/0009-0002-4125-6048

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Patients with inoperable or metastatic oropharyngeal squamous cell carcinoma (OSCC) face limited therapeutic options. Nectin-4, an immunoglobulin-like transmembrane adhesion protein, and Trophoblast Surface Antigen 2 (TROP2), a transmembrane glycoprotein, have recently emerged as targets for antibody-drug conjugates (ADCs). Objectives: This study aimed to demonstrate expression rates of TROP2 and Nectin-4 in a representative cohort of human papillomavirus (HPV)-positive and HPV-negative OSCC and discuss the relevance of those markers as possible targets for ADCs. Design: A retrospective cohort study. Methods: We analyzed tissue samples from 226 OSCC patients treated at the University Hospital of Cologne between 2005 and 2020. The expression of Nectin-4 and TROP2 was assessed using immunohistochemistry, and the H-score method was applied to categorize expression levels into four groups: negative (0-10), low (11-100), moderate (101-200), and high (201-300). Results: TROP2 expression was positive in 96.5% of the samples, with 84.1% showing moderate to high expression (H-Score 101-300). A total of 38.8% of the cases expressed Nectin-4. Notably, patients with HPV-positive OSCC demonstrated significantly higher Nectin-4 expression compared to those with HPV-negative OSCC ( Conclusion: This study is one of the first to investigate the expression of Nectin-4 and TROP2 in a cohort of both HPV-positive and HPV-negative OSCC patients. Our results indicate that TROP2 is almost universally expressed in OSCC, while Nectin-4 expression is less frequent. TROP2 and Nectin-4 are promising therapeutic targets for OSCC, with Nectin-4 being particularly relevant for HPV-positive patients. Clinical trials are necessary to confirm the clinical relevance and efficacy of ADCs targeting TROP2 and Nectin-4 in OSCC treatment.

Indexed as

antibody–drug conjugatesenfortumab vedotinHPVNectin-4oropharyngeal carcinomasacituzumab govitecantargeted therapyTROP2

Identifiers

PMID40838147
PMCPMC12361728

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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.