Evidence map›Paper›PMID 40981404›Full record

ArticleCancer medicine2025

One-Step Nucleic Acid Amplification Analysis of Sentinel Lymphatic Nodes in Endometrial Cancer Patients (EU-OSNA): A European Multicenter Diagnostic Accuracy Study.

Jan Kostun, Krzysztof Nowosielski, Marcin A Jedryka, David Hardisson, Stefano Restaino, Sonia Gatius, Zoltan Novak, Amaia Sagasta Lacalle, Susana Lopez, Martin Pešta and 19 more

Abstract readMulticenter Study
In one paragraph

Article in Cancer medicine, 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

29 authors.

Jan KostunDepartment of Gynecology and Obstetrics, University Hospital in Pilsen, Charles University, Pilsen, Czech Republic.ORCID https://orcid.org/0000-0003-4077-9031
Krzysztof NowosielskiDepartment of Gynecology and Gynecological Oncology, University Clinical Center of Medical University of Silesia, Katowice, Poland.
Marcin A JedrykaDepartment of Oncological Gynecology, Lower Silesian Oncology, Pulmonology and Hematology Center, Wroclaw, Poland.
David HardissonDepartment of Pathology, Hospital Universitario La Paz, Madrid, Spain.ORCID https://orcid.org/0000-0002-2183-3699
Stefano RestainoClinic of Obstetrics and Gynecology, 'Santa Maria della Misericordia' University Hospital, Azienda Sanitaria Universitaria Friuli Centrale, Udine, Italy.
Sonia GatiusDepartment of Pathology, Hospital Universitari Arnau de Vilanova de Lleida, Oncological Pathology Group, IRBLleida, Universitat de Lleida, CIBERONC, Lleida, Spain.
Zoltan NovakDepartment of Gynecology, National Institute of Oncology, Budapest, Hungary.
Amaia Sagasta LacalleDepartment of Pathology, Hospital Universitario Araba, Osakidetza, Instituto de Investigación Sanitaria Bioaraba, Universidad del País Vasco UPV/EHU, Vitoria-Gasteiz, Spain.
Susana LopezDepartment of Pathology, Hospital Universitario y Politecnico La Fe, Valencia, Spain.
Martin PeštaFaculty of Medicine in Pilsen, Institute of Biology, Charles University, Pilsen, Czech Republic.ORCID https://orcid.org/0000-0001-8187-0566
Marcin ZebalskiDepartment of Gynecology and Gynecological Oncology, University Clinical Center of Medical University of Silesia, Katowice, Poland.
Piotr LepkaDepartment of Oncological Gynecology, Lower Silesian Oncology, Pulmonology and Hematology Center, Wroclaw, Poland.
María Dolores DiestroGynecologic Oncology Unit, Department of Gynecology and Obstetrics, Hospital Universitario La Paz, Madrid, Spain.
Giuseppe VizzielliClinic of Obstetrics and Gynecology, 'Santa Maria della Misericordia' University Hospital, Azienda Sanitaria Universitaria Friuli Centrale, Udine, Italy.ORCID https://orcid.org/0000-0002-2424-2691
Xavier Matias-GuiuDepartment of Pathology, Hospital Universitari Arnau de Vilanova de Lleida, Oncological Pathology Group, IRBLleida, Universitat de Lleida, CIBERONC, Lleida, Spain.
Tímea EchimDepartment of Gynecology, National Institute of Oncology, Budapest, Hungary.
Emma Natalia Camacho UrkarayDepartment of Pathology, Hospital Universitario Araba, Osakidetza, Instituto de Investigación Sanitaria Bioaraba, Universidad del País Vasco UPV/EHU, Vitoria-Gasteiz, Spain.
Iván RiendaDepartment of Pathology, Hospital Universitario y Politecnico La Fe, Valencia, Spain.
Robert SlunečkoSikl's Department of Pathology, University Hospital in Pilsen, Charles University, Pilsen, Czech Republic.
Andrzej CzekanskiDepartment of Oncological Gynecology, Lower Silesian Oncology, Pulmonology and Hematology Center, Wroclaw, Poland.
Alberto BerjónDepartment of Pathology, Hospital Universitario La Paz, Madrid, Spain.
Laura MariuzziDepartment of Medicine, University of Udine, Udine, Italy.
Ana VelascoDepartment of Pathology, Hospital Universitari Arnau de Vilanova de Lleida, Oncological Pathology Group, IRBLleida, Universitat de Lleida, CIBERONC, Lleida, Spain.
Judit BetenbukDepartment of Pathology, National Institute of Oncology, Budapest, Hungary.
Isabel Guerra MerinoDepartment of Pathology, Hospital Universitario Araba, Osakidetza, Instituto de Investigación Sanitaria Bioaraba, Universidad del País Vasco UPV/EHU, Vitoria-Gasteiz, Spain.
Pablo Padilla-IserteDepartment of Gynecologic Oncology, Hospital Universitario y Politecnico La Fe, Valencia, Spain.
Petr StráníkDepartment of Gynecology and Obstetrics, University Hospital in Pilsen, Charles University, Pilsen, Czech Republic.
Vendula SmoligováDepartment of Gynecology and Obstetrics, University Hospital in Pilsen, Charles University, Pilsen, Czech Republic.
Jiří PreslDepartment of Gynecology and Obstetrics, University Hospital in Pilsen, Charles University, Pilsen, Czech Republic.

Funding

European Union-Next Generation EUMATC Science AreaNational Institute for Cancer Research-NICR LX22NPO5102Sysmex Corporation
6 · The paper itself

Abstract

objectiveThis European multicenter study aimed to assess the diagnostic accuracy of one-step nucleic acid amplification (OSNA) as the primary endpoint by comparing this method with ultrastaging for the detection of sentinel node metastases in endometrial cancer patients.

methodsEuropean multicenter prospective performance study including data from 10 centers across 5 European countries. Each node, upon removal of surrounding adipose tissue, was sliced in 2 mm thick sections and equally distributed between ultrastaging and OSNA. OSNA is based on cytokeratin-19 detection, serving as a metastatic marker. Sensitivity, specificity, and concordance of OSNA versus ultrastaging were calculated at nodal and patient levels.

resultsSeven hundred forty-three sentinel nodes from 366 patients were evaluated. Compared to ultrastaging, OSNA showed concordance, specificity, and sensitivity of 95%, 97.6%, and 41.2% at the nodal level and 93.2%, 96.2%, and 47.8% at the patient level, respectively. In reverse analysis, when compared to OSNA, the ultrastaging showed a sensitivity of 45.2% and 45.8% at the nodal and patient levels, respectively. Irrespective of the size of metastasis, both methods agreed in 14 positive and 692 negative nodes (95%). This resulted in 24 (6.56%) patients with a positive OSNA and 23 (6.28%) patients with a positive ultrastaging finding. The number of discordant nodes was 47 (6.33%), 40 (85.1%) of them were micrometastases. Benign epithelial inclusions occurred in 4 nodes (0.54%) and 4 patients (1.09%).

conclusionCompared with ultrastaging, OSNA showed high concordance and specificity, but sensitivity was low-similar to ultrastaging compared with OSNA as an index test in reverse analysis. The main limitation in comparing the two approaches by splitting the sentinel nodes was the tissue allocation bias. As reflected in the number of discordant cases, especially at the micrometastases level. The distribution of patients with node metastases was comparable between the two methods at both the nodal and patient levels.

trial registrationGerman Clinical Trial Register: Nr. DRKS00021520.

Indexed as

Biomarkers, TumorEndometrial NeoplasmsNucleic Acid Amplification TechniquesSentinel Lymph NodeAdultAgedAged, 80 and overEuropeFemaleHumansKeratin-19Lymphatic MetastasisMiddle AgedNeoplasm StagingProspective StudiesSensitivity and SpecificityBiomarkers, TumorKeratin-19KRT19 protein, humanbenign epithelial inclusionsendometrial cancerOSNAsentinel nodeultrastaging

Identifiers

PMID40981404
PMCPMC12451817

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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.