Evidence map›Paper›PMID 37773079›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2023

Clinical Behavior and Molecular Landscape of Stage I p53-Abnormal Low-Grade Endometrioid Endometrial Carcinomas.

Amy Jamieson, Lisa Vermij, Claire J H Kramer, Jan J Jobsen, Ina Jürgemlienk-Schulz, Ludy Lutgens, Jan Willem Mens, Marie A D Haverkort, Annerie Slot, Remi A Nout and 12 more

Open access · hybridAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
8.9field-weighted citation impact, top 2% 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

12 citing papers in PubMed, 30 citations in OpenAlex.

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  11. Targeted and Shallow Whole-Genome Sequencing Identifies Therapeutic Opportunities in p53abn Endometrial Cancers.Clinical cancer research : an official journal of the American Association for Cancer Research · 2024
    Article
  12. Review
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 at 13 institutions in 7 countries.

Amy Jamieson *Department of Gynecology and Obstetrics, Division of Gynecologic Oncology, University of British Columbia, Vancouver, Canada.ORCID 0000-0002-3210-9102
Lisa Vermij *Department of Pathology, Leiden University Medical Center, Leiden, the Netherlands.ORCID 0000-0003-4687-5550
Claire J H KramerDepartment of Pathology, Leiden University Medical Center, Leiden, the Netherlands.ORCID 0000-0001-7399-6804
Jan J JobsenDepartment of Radiation Oncology, Medisch Spectrum Twente, Enschede, the Netherlands.ORCID 0000-0001-7663-0170
Ina Jürgemlienk-SchulzDepartment of Radiation Oncology, University Medical Center Utrecht, Utrecht, the Netherlands.ORCID 0000-0003-4911-006X
Ludy LutgensMAASTRO Clinic, Maastricht, the Netherlands.ORCID 0000-0002-2942-8858
Jan Willem MensDepartment of Radiation Oncology, Erasmus Medical Center, Rotterdam, the Netherlands.ORCID 0000-0002-6363-8410
Marie A D HaverkortRadiotherapiegroep Arnhem, Arnhem, the Netherlands.ORCID 0000-0001-6516-1380
Annerie SlotRadiotherapeutic Institute Friesland, Leeuwarden, the Netherlands.ORCID 0000-0002-3684-6898
Remi A NoutDepartment of Radiation Oncology, Leiden University Medical Center, Leiden, the Netherlands.ORCID 0000-0001-8011-2982
Jan OostingDepartment of Pathology, Leiden University Medical Center, Leiden, the Netherlands.ORCID 0000-0001-8894-1742
Joseph CarlsonDepartment of Pathology, University of Southern California, Los Angeles.ORCID 0000-0002-3006-4107
Brooke E HowittDepartment of Pathology, Stanford University School of Medicine, Palo Alto.ORCID 0000-0002-0309-6680
Philip P C IpDepartment of Pathology, University of Hong Kong, Pokfulam, Hong Kong SAR, China.ORCID 0000-0002-0493-9838
Sigurd F LaxDepartment of Pathology, Hospital Graz II, Medical University of Graz, Graz, and Johannes Kepler University, Linz, Austria.ORCID 0000-0002-3576-601X
W Glenn McCluggageDepartment of Pathology, Belfast Health and Social Care Trust, Belfast, Northern Ireland, United Kingdom.ORCID 0000-0001-9178-4370
Naveena SinghDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.ORCID 0000-0003-1782-1967
Jessica N McAlpineDepartment of Gynecology and Obstetrics, Division of Gynecologic Oncology, University of British Columbia, Vancouver, Canada.ORCID 0000-0001-6003-485X
Carien L CreutzbergDepartment of Radiation Oncology, Leiden University Medical Center, Leiden, the Netherlands.ORCID 0000-0002-7008-4321
Nanda HorewegDepartment of Radiation Oncology, Leiden University Medical Center, Leiden, the Netherlands.ORCID 0000-0002-8581-4753
C Blake GilksDepartment of Pathology and Laboratory Medicine, University of British Columbia, Vancouver, Canada.ORCID 0000-0001-7889-8250
Tjalling BosseDepartment of Pathology, Leiden University Medical Center, Leiden, the Netherlands.ORCID 0000-0002-6881-8437
Leiden University Medical Center · NLUniversity of British Columbia · CABelfast Health and Social Care Trust · GBErasmus MC · NLMaastro Clinic · NLMedical University of Graz · ATMedisch Spectrum Twente · NLPalo Alto University · USRadiotherapeutisch Instituut Friesland · NLRadiotherapiegroep · NLUniversity of Hong Kong · HKUniversity of Southern California · USUtrecht University · NL

Funding

KWF Kankerbestrijding (DCS) 11629KWF Kankerbestrijding (DCS) 12995KWF Kankerbestrijding (DCS) CKVO 90-01KWF Kankerbestrijding (DCS) CTKO 1990-01
6 · The paper itself

Abstract

purposeThe clinical significance of the p53-abnormal (p53abn) molecular subtype in stage I low-grade endometrioid endometrial carcinoma (EEC) is debated. We aimed to review pathologic and molecular characteristics, and outcomes of stage I low-grade p53abn EEC in a large international cohort. EXPERIMENTAL

designPreviously diagnosed stage I p53abn EC (POLE-wild-type, mismatch repair-proficient) low-grade EEC from Canadian retrospective cohorts and PORTEC-1&2 trials were included. Pathology review was performed by six expert gynecologic pathologists blinded to p53 status. IHC profiling, next-generation sequencing, and shallow whole-genome sequencing was performed. Kaplan-Meier method was used for survival analysis.

resultsWe identified 55 stage I p53abn low-grade EEC among 3,387 cases (2.5%). On pathology review, 17 cases (31%) were not diagnosed as low-grade EEC by any pathologists, whereas 26 cases (47%) were diagnosed as low-grade EEC by at least three pathologists. The IHC and molecular profile of the latter cases were consistent with low-grade EEC morphology (ER/PR positivity, patchy p16 expression, PIK3CA and PTEN mutations) but they also showed features of p53abn EC (TP53 mutations, many copy-number alterations). These cases had a clinically relevant risk of disease recurrence (5-year recurrence-free survival 77%), with pelvic and/or distant recurrences observed in 12% of the patients.

conclusionsA subset of p53abn EC is morphologically low-grade EEC and exhibit genomic instability. Even for stage I disease, p53abn low-grade EEC are at substantial risk of disease recurrence. These findings highlight the clinical relevance of universal p53-testing, even in low-grade EEC, to identify women at increased risk of recurrence.

Indexed as

Carcinoma, EndometrioidEndometrial NeoplasmsCanadaFemaleHumansNeoplasm Recurrence, LocalRetrospective StudiesTumor Suppressor Protein p53Tumor Suppressor Protein p53

Identifiers

PMID37773079
PMCPMC10690141
OpenAlexW4387157118

What OpenQuestion holds

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LicenceCC BY-NC-ND
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.