Evidence map›Paper›PMID 38669067›Full record

ArticleClinical cancer research : an official journal of the American Association for Cancer Research2024

Endometrioid Endometrial RNA Index Predicts Recurrence in Stage I Patients.

Corrine A Nief, Phoebe M Hammer, Aihui Wang, Vivek Charu, Amina Tanweer, Babak Litkouhi, Elizabeth Kidd, Andrew J Gentles, Brooke E Howitt

Abstract read
In one paragraph

Article in Clinical cancer research : an official journal of the American Association for Cancer Research, 2024. 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

9 authors.

Corrine A Nief *Stanford University School of Medicine, Stanford, California.ORCID 0000-0003-3870-4786
Phoebe M Hammer *Department of Pathology, Stanford University, Stanford, California.ORCID 0000-0002-4206-2002
Aihui WangDepartment of Pathology, Stanford University, Stanford, California.ORCID 0000-0002-4497-7441
Vivek CharuDepartment of Pathology, Stanford University, Stanford, California.ORCID 0000-0002-7147-9026
Amina TanweerDepartment of Pathology, Stanford University, Stanford, California.ORCID 0000-0002-8435-9170
Babak LitkouhiDepartment of Biomedical Data Science, Stanford University, Stanford, California.ORCID 0000-0003-3124-4350
Elizabeth KiddDepartment of Radiation Oncology, Stanford University, Stanford, California.ORCID 0000-0003-4749-4098
Andrew J GentlesDepartment of Pathology, Stanford University, Stanford, California.ORCID 0000-0002-0941-9858
Brooke E HowittDepartment of Pathology, Stanford University, Stanford, California.ORCID 0000-0002-0309-6680

Funding

Translational Oncology Research Program (Project-005)P30CA124435 · NCI · STANFORD UNIVERSITY · PI Vittorio Sebastiano · 2007 to 2026
$71.4M
NCI NIH HHS P30 CA124435
6 · The paper itself

Abstract

purposeRisk prediction with genomic and transcriptomic data has the potential to improve patient outcomes by enabling clinicians to identify patients requiring adjuvant treatment approaches, while sparing low-risk patients from unnecessary interventions. Endometrioid endometrial carcinoma (EEC) is the most common cancer in women in developed countries, and rates of endometrial cancer are increasing. EXPERIMENTAL

designWe collected a 105-patient case-control cohort of stage I EEC comprising 45 patients who experienced recurrence less than 6 years after excision, and 60 Fédération Internationale de Gynécologie et d'Obstétrique grade-matched controls without recurrence. We first utilized two RNA-based, previously validated machine learning approaches, namely, EcoTyper and Complexity Index in Sarcoma (CINSARC). We developed Endometrioid Endometrial RNA Index (EERI), which uses RNA expression data from 46 genes to generate a personalized risk score for each patient. EERI was trained on our 105-patient cohort and tested on a publicly available cohort of 263 patients with stage I EEC.

resultsEERI was able to predict recurrences with 94% accuracy in the training set and 81% accuracy in the test set. In the test set, patients assigned as EERI high-risk were significantly more likely to experience recurrence (30%) than the EERI low-risk group (1%) with a hazard ratio of 9.9 (95% CI, 4.1-23.8; P < 0.001).

conclusionsTumors with high-risk genetic features may require additional treatment or closer monitoring and are not readily identified using traditional clinicopathologic and molecular features. EERI performs with high sensitivity and modest specificity, which may benefit from further optimization and validation in larger independent cohorts.

Indexed as

Carcinoma, EndometrioidEndometrial NeoplasmsNeoplasm Recurrence, LocalNeoplasm StagingAdultAgedBiomarkers, TumorCase-Control StudiesFemaleGene Expression ProfilingGene Expression Regulation, NeoplasticHumansMachine LearningMiddle AgedPrognosisBiomarkers, Tumor

Identifiers

PMID38669067
PMCPMC13215768

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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.