Evidence map›Paper›PMID 31792358›Full record

ArticleScientific reports2019

Prognostic classification of endometrial cancer using a molecular approach based on a twelve-gene NGS panel.

Raquel López-Reig, Antonio Fernández-Serra, Ignacio Romero, Cristina Zorrero, Carmen Illueca, Zaida García-Casado, Andrés Poveda, José Antonio López-Guerrero

Abstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing 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

24 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Article
  5. Article
  6. Review
  7. Review
  8. Runt-related transcription factors in human carcinogenesis: a friend or foe?Journal of cancer research and clinical oncology · 2023
    Review
  9. Article
  10. The Role of Biomarkers in Guiding Clinical Decision-Making in Oncology.Journal of the advanced practitioner in oncology · 2023
    Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Components ofJournal of oncology · 2022
    Article
  18. Article
  19. Article
  20. 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

8 authors.

Raquel López-ReigLaboratory of Molecular Biology, Services of Fundación Instituto Valenciano de Oncología, Valencia, Spain.
Antonio Fernández-SerraLaboratory of Molecular Biology, Services of Fundación Instituto Valenciano de Oncología, Valencia, Spain.
Ignacio RomeroMedical Oncology, Fundación Instituto Valenciano de Oncología, Valencia, Spain.
Cristina ZorreroGynecology, Fundación Instituto Valenciano de Oncología, Valencia, Spain.
Carmen IlluecaPathology, Fundación Instituto Valenciano de Oncología, Valencia, Spain.
Zaida García-CasadoLaboratory of Molecular Biology, Services of Fundación Instituto Valenciano de Oncología, Valencia, Spain.
Andrés PovedaDepartment of Oncology, INITIA ONCOLOGY, Hospital Quirón Salud, Valencia, Spain.
José Antonio López-GuerreroLaboratory of Molecular Biology, Services of Fundación Instituto Valenciano de Oncología, Valencia, Spain. jalopez@fivo.org.ORCID http://orcid.org/0000-0002-7369-8388

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Endometrial Cancer (EC) is one of the most common malignancies in women in developed countries. Molecular characterization of different biotypes may improve clinical management of EC. The Cancer Genome Atlas (TCGA) project has revealed four prognostic EC subgroups: POLE, MSI; Copy Number Low (CNL) and Copy Number High (CNH). The goal of this study was to develop a method to classify tumors in any of the four EC prognostic groups using affordable molecular techniques. Ninety-six Formalin-Fixed Paraffin-embedded (FFPE) samples were sequenced following a NGS TruSeq Custom Amplicon low input (Illumina) protocol interrogating a multi-gene panel. MSI analysis was performed by fragment analysis using eight specific microsatellite markers. A Random Forest classification algorithm (RFA), considering NGS results, was developed to stratify EC patients into different prognostic groups. Our approach correctly classifies the EC patients into the four TCGA prognostic biotypes. The RFA assigned the samples to the CNH and CNL groups with an accuracy of 0.9753 (p < 0.001). The prognostic value of these groups was prospectively reproduced on our series both for Disease-Free Survival (p = 0.004) and Overall Survival (p = 0.030).Hence, with the molecular approach herein described, a precise and suitable tool that mimics the prognostic EC subtypes has been solved and validated. Procedure that might be introduced into routine diagnostic practices.

Indexed as

MutationArtificial IntelligenceEndometrial NeoplasmsFemaleHumansMicrosatellite InstabilityMutation RatePrognosis

Identifiers

PMID31792358
PMCPMC6889294

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.