Evidence map›Paper›PMID 41742842›Full record

SynthesisInternational journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics2026

Diagnostic accuracy of phosphatase and tensin homolog loss in differentiating between atypical endometrial hyperplasia/endometrioid intraepithelial neoplasia and non-atypical endometrial hyperplasia: A systematic review and meta-analysis.

Kristina Shcherbatiuk, Steffi Bultmann, Thomas Karn, Khayal Gasimli, Peter Wild, Sven Becker, Morva Tahmasbi Rad

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Kristina ShcherbatiukDepartment of Gynaecology and Obstetrics, Johann Wolfgang Goethe University, Frankfurt am Main, Germany.ORCID https://orcid.org/0000-0002-3773-6041
Steffi BultmannDepartment of Pathology, Johann Wolfgang Goethe University, Frankfurt am Main, Germany.
Thomas KarnDepartment of Gynaecology and Obstetrics, Johann Wolfgang Goethe University, Frankfurt am Main, Germany.ORCID https://orcid.org/0000-0002-3264-6573
Khayal GasimliDepartment of Gynaecology and Obstetrics, Johann Wolfgang Goethe University, Frankfurt am Main, Germany.ORCID https://orcid.org/0000-0003-1874-0341
Peter WildDepartment of Pathology, Johann Wolfgang Goethe University, Frankfurt am Main, Germany.
Sven BeckerDepartment of Gynaecology and Obstetrics, Johann Wolfgang Goethe University, Frankfurt am Main, Germany.ORCID https://orcid.org/0000-0003-1141-4826
Morva Tahmasbi RadDepartment of Gynaecology and Obstetrics, Johann Wolfgang Goethe University, Frankfurt am Main, Germany.ORCID https://orcid.org/0000-0003-2883-523X

Funding

Deutscher Akademischer Austauschdienst ID: 57693450
6 · The paper itself

Abstract

backgroundAccurate distinction between atypical endometrial hyperplasia/endometrioid intraepithelial neoplasia (AH/EIN) and non-atypical endometrial hyperplasia (EH) determines whether patients require hysterectomy or can be managed conservatively. Phosphatase and tensin homolog (PTEN) loss has been proposed as an immunohistochemical (IHC) marker to support diagnostic evaluation.

objectivesThis study evaluates the diagnostic value of PTEN IHC for the diagnosis of AH/EIN and to explore how PTEN assessment methods affect diagnostic performance.

methodPubMed, Cochrane Library, ClinicalTrials.gov, Scopus, Embase, MEDLINE, and Web of Science were searched from database inception up to June 1, 2025. Studies reporting PTEN IHC in women with histologically confirmed AH/EIN or non-atypical EH. Two reviewers independently screened records, extracted data, and assessed risk of bias with QUADAS-2. Pooled diagnostic estimates and summary receiver-operating characteristics (SROC) curves were calculated using a bivariate random-effects model with subgroup analysis and the IHC method.

resultsTwenty-seven studies (2274 women) were included. Pooled sensitivity was 58.0% (95% confidence interval [CI], 40.8-73.4) and specificity 84.7% (95% CI, 67-93.8). The diagnostic odds ratio was 3.695 (95% CI, 2.501-5.460), with an area under the SROC of 0.679. The PTEN assessment method based on percentage of stained cells and staining intensity showed the highest the area under the curve of 0.744 among the methods evaluated in the subgroup analysis.

conclusionsPTEN IHC assessment demonstrated good specificity and might serve as a complementary tool in diagnosing AH/EIN, helping to reduce the number of incorrect diagnoses of atypia and unnecessary hysterectomies in clinical practice. Its limited sensitivity precludes its use as a standalone marker. Standardized staining protocols and multi-marker strategies are needed. PROSPERO REGISTRATION: CRD42024607623, registration date the 29 October 2024.

Indexed as

Carcinoma, EndometrioidEndometrial HyperplasiaEndometrial NeoplasmsPTEN PhosphohydrolaseBiomarkers, TumorDiagnosis, DifferentialFemaleHumansImmunohistochemistrySensitivity and SpecificityBiomarkers, TumorPTEN PhosphohydrolasePTEN protein, humandiagnostic testsendometrial hyperplasiaimmunohistochemistrymeta‐analysisPTEN phosphohydrolasesystematic review

Identifiers

PMID41742842
PMCPMC13377286

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.