Evidence map›Paper›PMID 26224872›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2016

Integrative Protein-Based Prognostic Model for Early-Stage Endometrioid Endometrial Cancer.

Ji-Yeon Yang, Henrica M J Werner, Jie Li, Shannon N Westin, Yiling Lu, Mari K Halle, Jone Trovik, Helga B Salvesen, Gordon B Mills, Han Liang

Open access · bronzeAbstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

19 citing papers in PubMed, 29 citations in OpenAlex.

  1. Article
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  3. Association of insulin-like growth factor II mrna-binding protein 3 (IMP3) expression with prognostic and morphological factors in endometrial cancer.Revista brasileira de ginecologia e obstetricia : revista da Federacao Brasileira das Sociedades de Ginecologia e Obstetricia · 2024
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  10. Novel miRNA markers for the diagnosis and prognosis of endometrial cancer.Journal of cellular and molecular medicine · 2020
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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

10 authors at 3 institutions in 3 countries.

Ji-Yeon YangDepartment of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas. Department of Applied Mathematics, Kumoh National Institute of Technology, Gumi-si, South Korea.
Henrica M J WernerCentre for Cancer Biomarkers, Department of Clinical Science, The University of Bergen, Bergen, Norway. Department of Obstetrics and Gynecology, Haukeland University Hospital, Bergen, Norway.
Jie LiDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Shannon N WestinDepartment of Gynecologic Oncology and Reproductive Medicine, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Yiling LuDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas.
Mari K HalleCentre for Cancer Biomarkers, Department of Clinical Science, The University of Bergen, Bergen, Norway. Department of Obstetrics and Gynecology, Haukeland University Hospital, Bergen, Norway.
Jone TrovikCentre for Cancer Biomarkers, Department of Clinical Science, The University of Bergen, Bergen, Norway. Department of Obstetrics and Gynecology, Haukeland University Hospital, Bergen, Norway.
Helga B SalvesenCentre for Cancer Biomarkers, Department of Clinical Science, The University of Bergen, Bergen, Norway. Department of Obstetrics and Gynecology, Haukeland University Hospital, Bergen, Norway.
Gordon B MillsDepartment of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas. hliang1@mdanderson.org gmills@mdanderson.org.
Han LiangDepartment of Bioinformatics and Computational Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas. Department of Systems Biology, The University of Texas MD Anderson Cancer Center, Houston, Texas. hliang1@mdanderson.org gmills@mdanderson.org.
The University of Texas MD Anderson Cancer Center · USHaukeland University Hospital · NOKumoh National Institute of Technology · KR

Funding

Tumor Evolution and Metastasis ProgramP30CA016672 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI Scott Kopetz · 1985 to 2026
$290.8M
Targeting the PI3K Signaling Pathway in Endometrial CarcinomaP50CA098258 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI BODURKA, DIANE · 2003 to 2020
$32.0M
Paul Calabresi Clinical Oncology AwardK12CA088084 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI David S. Hong, Scott Kopetz · 2000 to 2026
$14.0M
Integrative Pipeline for Analysis & Translational Application of TCGA Data (GDAC)U24CA143883 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI AKBANI, REHAN, MILLS, GORDON B. · 2009 to 2016
$10.6M
Systematic Functional Characterization of RNA Editing in Endometrial CancerR01CA175486 · NCI · UNIVERSITY OF TX MD ANDERSON CAN CTR · PI LIANG, HAN · 2014 to 2018
$1.7M
NCI NIH HHS CA016672NCI NIH HHS CA088084NCI NIH HHS CA098258NCI NIH HHS CA143883NCI NIH HHS CA175486NCI NIH HHS K12 CA088084NCI NIH HHS P30 CA016672NCI NIH HHS P50 CA098258NCI NIH HHS R01 CA175486NCI NIH HHS U24 CA143883
6 · The paper itself

Abstract

purposeEndometrioid endometrial carcinoma (EEC) is the major histologic type of endometrial cancer, the most prevalent gynecologic malignancy in the United States. EEC recurrence or metastasis is associated with a poor prognosis. Early-stage EEC is generally curable, but a subset has high risk of recurrence or metastasis. Prognosis estimation for early-stage EEC mainly relies on clinicopathologic characteristics, but is unreliable. We aimed to identify patients with high-risk early-stage EEC who are most likely to benefit from more extensive surgery and adjuvant therapy by building a prognostic model that integrates clinical variables and protein markers. EXPERIMENTAL

designWe used two large, independent early-stage EEC datasets as training (n = 183) and validation cohorts (n = 333), and generated the levels of 186 proteins and phosphoproteins using reverse-phase protein arrays. By applying an initial filtering and the elastic net to the training samples, we developed a prognostic model for overall survival containing two clinical variables and 18 protein markers and optimized the risk group classification.

resultsThe Kaplan-Meier survival analyses in the validation cohort confirmed an improved discriminating power of our prognostic model for patients with early-stage EEC over key clinical variables (log-rank test, P = 0.565 for disease stage, 0.567 for tumor grade, and 1.3 × 10(-4) for the integrative model). Compared with clinical variables (stage, grade, and patient age), only the risk groups defined by the integrative model were consistently significant in both univariate and multivariate analyses across both cohorts.

conclusionsOur prognostic model is potentially of high clinical value for stratifying patients with early-stage EEC and improving their treatment strategies.

Indexed as

AdultAgedAged, 80 and overBiomarkers, TumorCarcinoma, EndometrioidDisease-Free SurvivalEndometrial NeoplasmsFemaleHumansKaplan-Meier EstimateMiddle AgedNeoplasm Recurrence, LocalNeoplasm StagingPrognosisProteinsYoung AdultBiomarkers, TumorProteins

Identifiers

PMID26224872
PMCPMC4715969
OpenAlexW948425943

What OpenQuestion holds

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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.