Evidence map›Paper›PMID 40792549›Full record

ArticleHistopathology2026

Endometrial carcinoma and immune escape: prognostic relevance of HLA class I loss in NSMP subtype.

Marco Grillini, Jacopo Lenzi, Claudio Ceccarelli, Dario de Biase, Thais Maloberti, Sara Coluccelli, Laura Poppi, Riccardo Ciudino, Caterina Ravaioli, Camelia Alexandra Coadǎ and 12 more

Abstract read
In one paragraph

Article in Histopathology, 2026. 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

22 authors.

Marco GrilliniPathology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0003-2506-7239
Jacopo LenziDepartment of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0003-2882-4223
Claudio CeccarelliDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0003-0743-2087
Dario de BiaseDepartment of Pharmacy and Biotechnology (FaBit), University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0002-0609-8817
Thais MalobertiSolid Tumor Molecular Pathology Laboratory, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0002-8306-4653
Sara ColuccelliSolid Tumor Molecular Pathology Laboratory, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0002-1475-4044
Laura PoppiSolid Tumor Molecular Pathology Laboratory, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Riccardo CiudinoDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy.ORCID https://orcid.org/0009-0006-7245-584X
Caterina RavaioliPathology Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.ORCID https://orcid.org/0009-0002-8556-8756
Camelia Alexandra CoadǎUniversity of Medicine and Pharmacy "Iuliu Hatieganu", Cluj-Napoca, Romania.ORCID https://orcid.org/0000-0001-8362-6639
Gloria RavegniniDepartment of Pharmacy and Biotechnology (FaBit), University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0002-7774-402X
Anna Myriam PerroneDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0003-3140-4772
Pierandrea De IacoDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0002-8841-6531
Daniela RubinoAddarii Medical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.
Claudio ZamagniAddarii Medical Oncology, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0002-7143-9091
Benedetta DonatiLaboratory of Translational Research, Arcispedale Santa Maria Nuova, Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia, Reggio Emilia, Italy.ORCID https://orcid.org/0000-0002-9163-8194
Alessia CiarrocchiLaboratory of Translational Research, Arcispedale Santa Maria Nuova, Azienda Unità Sanitaria Locale-IRCCS di Reggio Emilia, Reggio Emilia, Italy.ORCID https://orcid.org/0000-0002-5541-2075
Sabrina CroceDepartment of Biopathology, Institut Bergonié, Bordeaux, France.ORCID https://orcid.org/0000-0002-6487-5418
Martin KöbelDepartment of Pathology and Laboratory Medicine, University of Calgary, Calgary, Alberta, Canada.ORCID https://orcid.org/0000-0002-6615-2037
Cheng-Han LeeDepartment of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada.ORCID https://orcid.org/0000-0003-2094-1222
Giovanni TalliniDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0003-0113-6682
Antonio De LeoDepartment of Medical and Surgical Sciences (DIMEC), University of Bologna, Bologna, Italy.ORCID https://orcid.org/0000-0002-3761-5135

Funding

Fondazione AIRC per la ricerca sul cancro ETS
6 · The paper itself

Abstract

aimsThis study aims to define and characterize human leukocyte antigen class I (HLA-I) expression in a consecutive series of molecularly classified endometrial carcinomas (ECs), and to evaluate its association with clinicopathologic features, spatial cancer-immune phenotypes and patient prognosis, with a focus on the NSMP (no specific molecular profile) subtype. METHODS AND

resultsHLA-I expression was assessed by immunohistochemistry on whole tissue sections from 208 ECs, classified into POLE-mutated, MMR-deficient (MMRd), p53-abnormal (p53abn) and NSMP subtypes. Loss of HLA-I was identified in 31% of cases and was associated with adverse features including high-grade, aggressive histotypes, deep myometrial invasion, substantial lymphovascular space invasion (LVSI), extensive tumour necrosis and an 'excluded' immune phenotype. While HLA-I loss showed no significant prognostic impact in POLE, MMRd or p53abn tumours, it significantly correlated with worse disease-free survival in NSMP tumours (P < 0.001). Multivariate analysis confirmed HLA-I loss as an independent prognostic factor in early-stage NSMP ECs, in addition to substantial LVSI, presence of lymph node metastases and spatial cancer-immune phenotypes. Integration of HLA-I status improved the performance of predictive models over time.

conclusionsHLA-I loss defines a biologically aggressive subgroup within NSMP ECs and is associated with adverse clinicopathologic and immune features. Assessment of HLA-I expression could refine risk stratification in NSMP ECs, a group traditionally lacking robust prognostic markers and may help identify patients who could benefit from intensified clinical surveillance and future immunomodulatory treatment strategies.

Indexed as

CarcinomaEndometrial NeoplasmsHistocompatibility Antigens Class ILoss of HeterozygosityTumor EscapeAdultAgedAged, 80 and overBiomarkers, TumorClinical RelevanceFemaleHumansImmunohistochemistryKaplan-Meier EstimateMiddle AgedPrognosisBiomarkers, TumorHistocompatibility Antigens Class Iendometrial carcinomahistopathological parametersHLA‐Iimmune phenotypemolecular classificationrisk stratificationtumour microenvironment

Identifiers

PMID40792549
PMCPMC12703446

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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.