Evidence map›Paper›PMID 33858677›Full record

ArticleGynecologic oncology2021

Immunohistochemical biomarkers are prognostic relevant in addition to the ESMO-ESGO-ESTRO risk classification in endometrial cancer.

S W Vrede, W J van Weelden, N C M Visser, J Bulten, L J M van der Putten, K van de Vijver, M Santacana, E Colas, A Gil-Moreno, C P Moiola and 17 more

Open access · hybridAbstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in Gynecologic oncology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

17 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Prognostic Role of L1CAM in Endometrial Cancer.Diagnostics (Basel, Switzerland) · 2025
    Review
  6. Article
  7. Article
  8. Article
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  12. Review
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  16. Cancer of the corpus uteri: 2021 update.International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics · 2021
    Article
  17. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

27 authors at 16 institutions in 7 countries.

S W VredeDepartment of Obstetrics and Gynaecology, Radboud university medical center, Nijmegen, the Netherlands; Department of Obstetrics and Gynaecology, Canisius-Wilhelmina Hospital, Nijmegen, the Netherlands. Electronic address: stephanie.vrede@radboudumc.nl.
W J van WeeldenDepartment of Obstetrics and Gynaecology, Radboud university medical center, Nijmegen, the Netherlands.
N C M VisserDepartment of Pathology, Stichting PAMM, Eindhoven, the Netherlands; Department of Pathology, Radboud university medical center, Nijmegen, the Netherlands.
J BultenDepartment of Pathology, Radboud university medical center, Nijmegen, the Netherlands.
L J M van der PuttenDepartment of Obstetrics and Gynaecology, Radboud university medical center, Nijmegen, the Netherlands.
K van de VijverDepartment of Pathology, Ghent University Hospital, Cancer Research Institute Ghent (CRIG), Ghent, Belgium.
M SantacanaDepartment of Pathology and Molecular Genetics and Research Laboratory, Hospital Universitari Arnau de Vilanova, University of Lleida, IRBLleida, CIBERONC, Lleida, Spain.
E ColasBiomedical Research Group in Gynaecology, Vall Hebron Institute of Research, Universitat Autònoma de Barcelona, CIBERONC, Barcelona, Spain.
A Gil-MorenoGynecological Department, Vall Hebron University Hospital, CIBERONC, Barcelona, Spain; Pathology Department, Vall Hebron University Hospital, CIBERONC, Barcelona, Spain.
C P MoiolaBiomedical Research Group in Gynaecology, Vall Hebron Institute of Research, Universitat Autònoma de Barcelona, CIBERONC, Barcelona, Spain.
G ManceboDepartment of Obstetrics and Gynaecology, Hospital del Mar, PSMAR, Barcelona, Spain.
C KrakstadDepartment of Obstetrics and Gynaecology, Haukeland University Hospital, Bergen, Norway; Centre for Cancer Biomarkers, Department of Clinical Science, University of Bergen, Bergen, Norway.
J TrovikDepartment of Obstetrics and Gynaecology, Haukeland University Hospital, Bergen, Norway.
I S HaldorsenCentre for Cancer Biomarkers, Department of Clinical Science, University of Bergen, Bergen, Norway; Mohn Medical Imaging and Visualization Centre, Department of Radiology, Haukeland University Hospital, Bergen, Norway.
J HuvilaDepartment of Pathology, University of Turku, Turku, Finland.
M KoskasDepartment of Obstetrics and Gynaecology Department, Bichat-Claude Bernard Hospital, Paris, France.
V WeinbergerDepartment of Obstetrics and Gynaecology, University Hospital in Brno and Masaryk University, Brno, Czech Republic.
M BednarikovaDepartment of Internal Medicine, Hematology and Oncology, University Hospital in Brno and Masaryk University, Brno, Czech Republic.
J HausnerovaDepartment of Pathology, University Hospital in Brno and Masaryk University, Brno, Czech Republic.
A A van der WurffDepartment of Pathology, Elisabeth-TweeSteden Hospital, Tilburg, the Netherlands.
X Matias-GuiuDepartment of Pathology and Molecular Genetics and Research Laboratory, Hospital Universitari Arnau de Vilanova, University of Lleida, IRBLleida, CIBERONC, Lleida, Spain.
F AmantDepartment of Oncology, KU Leuven, Leuven, Belgium; Department of Gynaecologic Oncology, Netherlands Cancer Institute and Amsterdam Medical Centers, Amsterdam, the Netherlands.
ENITEC Consortium
M P L M SnijdersDepartment of Obstetrics and Gynaecology, Canisius-Wilhelmina Hospital, Nijmegen, the Netherlands.
H V N Küsters-VandeveldeDepartment of Pathology, Canisius-Wilhelmina Hospital, Nijmegen, the Netherlands.
C ReijnenDepartment of Radiation Oncology, Radboud university medical center, Nijmegen, the Netherlands.
J M A PijnenborgDepartment of Obstetrics and Gynaecology, Radboud university medical center, Nijmegen, the Netherlands.
Radboud University Medical Center · NLMasaryk University · CZRadboud University Nijmegen · NLCanisius-Wilhelmina Ziekenhuis · NLCentro de Investigación Biomédica en Red de Cáncer · ESHaukeland University Hospital · NOBiomedical Research Institute of Lleida · ESCancer Research Institute Ghent · BEElisabeth-TweeSteden Ziekenhuis · NLHospital Del Mar · ESThe Netherlands Cancer Institute · NLUniversitat de Lleida · ESUniversité Claude Bernard Lyon 1 · FRUniversity of Bergen · NOUniversity of Turku · FIVall d'Hebron Hospital Universitari · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivePre-operative immunohistochemical (IHC) biomarkers are not incorporated in endometrial cancer (EC) risk classification. We aim to investigate the added prognostic relevance of IHC biomarkers to the ESMO-ESGO-ESTRO risk classification and lymph node (LN) status in EC.

methodsRetrospective multicenter study within the European Network for Individualized Treatment of Endometrial Cancer (ENITEC), analyzing pre-operative IHC expression of p53, L1 cell-adhesion molecule (L1CAM), estrogen receptor (ER) and progesterone receptor (PR), and relate to ESMO-ESGO-ESTRO risk groups, LN status and outcome.

resultsA total of 763 EC patients were included with a median follow-up of 5.5-years. Abnormal IHC expression was present for p53 in 112 (14.7%), L1CAM in 79 (10.4%), ER- in 76 (10.0%), and PR- in 138 (18.1%) patients. Abnormal expression of p53/L1CAM/ER/PR was significantly related with higher risk classification groups, and combined associated with the worst outcome within the 'high and advanced/metastatic' risk group. In multivariate analysis p53-abn, ER/PR- and ESMO-ESGO-ESTRO 'high and advanced/metastatic' were independently associated with reduced disease-specific survival (DSS). Patients with abnormal IHC expression and lymph node metastasis (LNM) had the worst outcome. Patients with LNM and normal IHC expression had comparable outcome with patients without LNM and abnormal IHC expression.

conclusionThe use of pre-operative IHC biomarkers has important prognostic relevance in addition to the ESMO-ESGO-ESTRO risk classification and in addition to LN status. For daily clinical practice, p53/L1CAM/ER/PR expression could serve as indicator for surgical staging and refine selective adjuvant treatment by incorporation into the ESMO-ESGO-ESTRO risk classification.

Indexed as

AgedBiomarkers, TumorCohort StudiesEndometrial NeoplasmsEuropeFemaleHumansLymphatic MetastasisNeural Cell Adhesion Molecule L1Predictive Value of TestsPrognosisRetrospective StudiesRisk FactorsSurvival AnalysisBiomarkers, TumorNeural Cell Adhesion Molecule L1BiomarkerEndometrial carcinomaImmunohistochemistryLymph node metastasisOutcome

Identifiers

PMID33858677
OpenAlexW3155989883

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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.