Evidence map›Paper›PMID 39731204›Full record

ArticleHistopathology2025

Expression of claudin-18.2 in cholangiocarcinoma: a comprehensive immunohistochemical analysis from a German tertiary centre.

Maximilian N Kinzler, Steffen Gretser, Falko Schulze, Katrin Bankov, Nada Abedin, Wolf O Bechstein, Fabian Finkelmeier, Stefan Zeuzem, Henning Reis, Peter J Wild and 1 more

Abstract read
In one paragraph

Article in Histopathology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing 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

13 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
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  5. Review
  6. Article
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  8. Review
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  11. Review
  12. Article
  13. Claudin 18 immunohistochemistry in cholangiocarcinoma.Journal of gastrointestinal oncology · 2025
    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

11 authors.

Maximilian N KinzlerGoethe University Frankfurt, Medical Clinic 1, University Hospital, Frankfurt am Main, Germany.ORCID https://orcid.org/0000-0003-2378-1455
Steffen GretserGoethe University Frankfurt, Dr. Senckenberg Institute of Pathology, University Hospital, Frankfurt am Main, Germany.
Falko SchulzeGoethe University Frankfurt, Dr. Senckenberg Institute of Pathology, University Hospital, Frankfurt am Main, Germany.
Katrin BankovGoethe University Frankfurt, Dr. Senckenberg Institute of Pathology, University Hospital, Frankfurt am Main, Germany.
Nada AbedinGoethe University Frankfurt, Medical Clinic 1, University Hospital, Frankfurt am Main, Germany.
Wolf O BechsteinDepartment of General, Visceral, Transplant and Thoracic Surgery, University Hospital, Goethe University Frankfurt, Frankfurt am Main, Germany.
Fabian FinkelmeierGoethe University Frankfurt, Medical Clinic 1, University Hospital, Frankfurt am Main, Germany.ORCID https://orcid.org/0000-0001-8559-9910
Stefan ZeuzemGoethe University Frankfurt, Medical Clinic 1, University Hospital, Frankfurt am Main, Germany.ORCID https://orcid.org/0000-0002-0845-6833
Henning ReisGoethe University Frankfurt, Dr. Senckenberg Institute of Pathology, University Hospital, Frankfurt am Main, Germany.
Peter J WildGoethe University Frankfurt, Dr. Senckenberg Institute of Pathology, University Hospital, Frankfurt am Main, Germany.
Dirk WalterGoethe University Frankfurt, Medical Clinic 1, University Hospital, Frankfurt am Main, Germany.ORCID https://orcid.org/0000-0003-2309-9624

Funding

Frankfurt Research Promotion Program (FFF) of the Faculty of Medicine of the Goethe University
6 · The paper itself

Abstract

aimsAnti-claudin-18.2 (CLDN18.2) therapy was recently approved for the treatment of gastric or gastro-oesophageal junction adenocarcinoma. The aim of the present study was to investigate the expression of CLDN18.2 in cholangiocarcinoma (CCA) to determine whether there is a subgroup of patients who might also benefit from anti-CLDN18.2 therapy. METHODS AND

resultsA tissue microarray (TMA) cohort of all CCA patients who underwent surgical resection with curative intent between August 2005 and December 2021 at University Hospital Frankfurt were immunohistochemically evaluated using the VENTANA

conclusionsThe present study suggests that a subset of patients with CCA exhibited a marked expression of CLDN18.2. These findings underline the need to perform a clinical study evaluating the efficacy of anti-CLDN18.2 therapy in patients suffering from CCA.

Indexed as

Bile Duct NeoplasmsBiomarkers, TumorCholangiocarcinomaClaudinsAdultAgedAged, 80 and overFemaleGermanyHumansImmunohistochemistryMaleMiddle AgedTertiary Care CentersTissue Array AnalysisBiomarkers, TumorClaudinsCLDN18 protein, humanbiomarkercholangiocarcinomaCLDN18surgical oncologytight junctions

Identifiers

PMID39731204
PMCPMC11791722

What OpenQuestion holds

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Registered trials

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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.