Evidence map›Paper›PMID 41986616›Full record

ArticleBJC reports2026

High expression of the ADC target Claudin-6 associates with aggressive endometrial cancer and remains high in metastatic lesions.

Vilde Linnea Gullovsen, Daniela Pavlicenco, Marta E Hjelmeland, Kathrine Woie, Ingfrid S Haldorsen, Jone Trovik, Hege F Berg, Camilla Krakstad

Abstract read
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Article in BJC reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Vilde Linnea GullovsenCentre for Cancer Biomarkers, Department of Clinical Science, University of Bergen, Bergen, Norway.
Daniela PavlicencoCentre for Cancer Biomarkers, Department of Clinical Science, University of Bergen, Bergen, Norway.
Marta E HjelmelandCentre for Cancer Biomarkers, Department of Clinical Science, University of Bergen, Bergen, Norway.
Kathrine WoieDepartment of Gynecology and Obstetrics, Haukeland University Hospital, Bergen, Norway.
Ingfrid S HaldorsenDepartment of Clinical Medicine, University of Bergen, Bergen, Norway.
Jone TrovikCentre for Cancer Biomarkers, Department of Clinical Science, University of Bergen, Bergen, Norway.
Hege F BergCentre for Cancer Biomarkers, Department of Clinical Science, University of Bergen, Bergen, Norway.
Camilla KrakstadCentre for Cancer Biomarkers, Department of Clinical Science, University of Bergen, Bergen, Norway. camilla.krakstad@uib.no.ORCID http://orcid.org/0000-0002-0174-8139

Funding

Helse Vest F13103Kreftforeningen 223283Norges Forskningsråd 326348
6 · The paper itself

Abstract

backgroundPatients with advanced or recurrent endometrial cancer (EC) have limited treatment options. The development of antibody-drug conjugates (ADCs) offers new treatment strategies by targeted delivery of cytotoxic payloads, including conventional chemotherapy, to cancer cells. An ADC targeting Claudin-6 is currently in clinical testing however expression patterns of Claudin-6 has not been thoroughly explored in EC.

methodsMembrane expression of Claudin-6 was evaluated by immunohistochemistry in a large, prospectively collected EC cohort with 1106 primary tumours and 187 metastatic lesions. Claudin-6 expression was scored according to the Gastric criteria and correlated with clinicopathological characteristics and follow-up data.

resultsClaudin-6 expression was detected in 18% of ECs and was highly expressed in 10% of all samples. High expression was observed in 49% of serous tumours and 22% of carcinosarcomas. High Claudin-6 independently predicted poor disease-specific survival in multivariate analysis (HR: 1.7, CI: 1.2-2.4, p = 0.002). In the paired primary-metastasis cohort, Claudin-6 was highly expressed in 19% of primary tumours and, of these, 77% maintained high expression in at least one corresponding metastatic lesion.

conclusionsOur study identified Claudin-6 as an independent prognostic marker in EC and as a potential target for ADCs, particularly in serous and carcinosarcoma subtypes.

Identifiers

PMID41986616
PMCPMC13083938

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