Evidence map›Paper›PMID 35038071›Full record

ReviewInternational journal of clinical oncology2022

High-intermediate risk endometrial cancer: moving toward a molecularly based risk assessment profile.

Tavonna D Kako, Maahum Z Kamal, Jhalak Dholakia, Carly B Scalise, Rebecca C Arend

Registry-linked trialAbstract readReview
PubMed Publisher
In one paragraph

Review in International journal of clinical oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07339384 (Circulating Tumor DNA Assessment in Early-Stage Endometrial Cancer), which is not on this map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.6field-weighted citation impact, top 35% 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.

NCT07339384 nanot yet recruitingnot on this mapstarted 2026, after this paper: background citation

Circulating Tumor DNA Assessment in Early-Stage Endometrial Cancer (SIGNAL-EMC 101)

TypeinterventionalSponsorNatera, Inc.Ran2026 to 2034Enrolled1,010ConditionsEndometrial CancerArmsSignatera Genome ultra-sensitive ctDNA blood test
3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 3 citations in OpenAlex.

  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

5 authors at 1 institution in 1 country.

Tavonna D Kako *Department of Obstetrics and Gynecology, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
Maahum Z Kamal *University of Alabama at Birmingham School of Medicine, Birmingham, AL, 35294, USA.
Jhalak DholakiaDepartment of Obstetrics and Gynecology, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
Carly B ScaliseDepartment of Obstetrics and Gynecology, University of Alabama at Birmingham, Birmingham, AL, 35294, USA.
Rebecca C ArendDepartment of Obstetrics and Gynecology, University of Alabama at Birmingham, Birmingham, AL, 35294, USA. rarend@uabmc.edu.
University of Alabama at Birmingham · US

Funding

UAB Cancer Prevention and Control Training Program (T32)T32CA047888 · NCI · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI Ritu Aneja, Ellen Mary Lavoie Smith · 2018 to 2026
$3.2M
Foundation for Women's Cancer Clinical Research Award for Endometrial CancerFoundation for Women's Cancer Wilma Williams Education
6 · The paper itself

Abstract

In the USA, endometrial cancer (EMCA) incidence is increasing as the risk factors of obesity, diabetes, and hypertension become more prevalent. Although most EMCA is detected at an early stage and surgical intervention is curative, a subset of patients termed 'high-intermediate risk' (H-IR) experience an increased rate of recurrence. Unfortunately, adjuvant therapies in patients with H-IR EMCA have yet to increase overall survival. Historically, stratification of these patients from their low-risk counterparts incorporated clinical and pathologic findings. However, due to developments in molecular testing and genomic sequencing, tumor biomarkers are now being incorporated into the risk-assessment criteria in the hope of finding molecular profile(s) that could highlight treatment regimens that will increase patient survival. Since modern research aims to accurately identify patients with a higher risk of recurrence and develop effective interventions to improve patient survival, these molecular-based analyses could allow for an enhanced understanding of a patient's true risk of recurrence to facilitate the rise of personalized medicine. This review summarizes key clinical trials and recent advances in molecular and genomic profiles that have influenced current treatment regimens for patients with H-IR EMCA and laid the foundation for subsequent research.

Indexed as

Endometrial NeoplasmsBiomarkers, TumorCombined Modality TherapyFemaleHumansObesityRisk AssessmentBiomarkers, TumorEndometrial cancerHigh-intermediate riskMolecular profile

Identifiers

PMID35038071
OpenAlexW4206383058

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

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.