Evidence map›Paper›PMID 39487683›Full record

ArticleCancer medicine2024

A Multicenter Cohort Study on DNA Methylation for Endometrial Cancer Detection in Cervical Scrapings.

Xiao Ma, Xiaojun Chen, Jing Liang, Jingbo Zhang, Qixi Wu, Dong Wang, Xianghua Huang, Dan Zi, Dexin Chen, Hua Wan and 13 more

Abstract readMulticenter Study
In one paragraph

Article in Cancer medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. 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

23 authors.

Xiao MaDepartment of Obstetrics and Gynecology, National Clinical Research Center for Obstetric & Gynecologic Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, China.
Xiaojun ChenDepartment of Gynecologic Oncology, Obstetrics and Gynecology Hospital of Fudan University, Shanghai, China.
Jing LiangDepartment of Obstetrics and Gynecology, China-Japan Friendship Hospital, Beijing, China.
Jingbo ZhangDepartment of Medicine, Beijing USCI Medical Laboratory, Beijing, China.
Qixi WuDepartment of Medicine, Beijing USCI Medical Laboratory, Beijing, China.
Dong WangDepartment of Gynecologic Oncology, Chongqing University Cancer Hospital, Chongqing, China.
Xianghua HuangDepartment of Gynecology, Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Dan ZiDepartment of Gynecology, Guizhou Provincial People's Hospital, Guiyang, Guizhou, China.
Dexin ChenDepartment of Gynecology, Sichuan Provincial Maternity and Child Health Care Hospital, Chengdu, Sichuan, China.
Hua WanDepartment of Medicine, Beijing USCI Medical Laboratory, Beijing, China.
Li QuDepartment of Medicine, Beijing USCI Medical Laboratory, Beijing, China.
Zhaoyun JiangDepartment of Medicine, Beijing USCI Medical Laboratory, Beijing, China.ORCID https://orcid.org/0000-0001-5441-7504
Wenyu ShaoDepartment of Gynecologic Oncology, Obstetrics and Gynecology Hospital of Fudan University, Shanghai, China.ORCID https://orcid.org/0000-0001-8853-1735
Jie SunDepartment of Obstetrics and Gynecology, China-Japan Friendship Hospital, Beijing, China.
Luyuan ChangDepartment of Medicine, Beijing USCI Medical Laboratory, Beijing, China.
Yunchao LiuDepartment of Medicine, Beijing USCI Medical Laboratory, Beijing, China.
Qin ZhangDepartment of Gynecologic Oncology, Chongqing University Cancer Hospital, Chongqing, China.
Yanan LiDepartment of Gynecology, Second Hospital of Hebei Medical University, Shijiazhuang, Hebei, China.
Yani DingDepartment of Gynecology, Guizhou Provincial People's Hospital, Guiyang, Guizhou, China.
Biao TangDepartment of Gynecology, Sichuan Provincial Maternity and Child Health Care Hospital, Chengdu, Sichuan, China.
Fang ZhaoDepartment of Obstetrics and Gynecology, China-Japan Friendship Hospital, Beijing, China.
Hanqing ZhaoDepartment of Medicine, Beijing USCI Medical Laboratory, Beijing, China.
Dongyan CaoDepartment of Obstetrics and Gynecology, National Clinical Research Center for Obstetric & Gynecologic Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Peking Union Medical College, Beijing, China.ORCID https://orcid.org/0000-0003-4253-832X

Funding

National High-Level Hospital Clinical Research Funding 2022-PUMCH-B-082
6 · The paper itself

Abstract

backgroundThe increasing incidence of endometrial cancer (EC) has highlighted the need for improved early detection methods. This study aimed to develop and validate a novel DNA methylation classifier, EMPap, for EC detection using cervical scrapings.

methodsEMPap incorporated the methylation status of BHLHE22 and CDO1, along with age and body mass index (BMI), into a logistic regression model to calculate the endometrial cancer methylation (EM) score for identifying EC in cervical scrapings. We enrolled 1297 patients with highly suspected EC, including 196 confirmed EC cases, and assessed the EMPap performance in detecting EC.

resultsEMPap demonstrated robust diagnostic accuracy, with an area under the curve of 0.93, sensitivity of 90.3%, and specificity of 89.3%. It effectively detected EC across various disease stages, grades, and histological subtypes, and consistently performed well across patient demographics and symptoms. EMPap correctly identified 87.5% of the type II ECs and 53.8% of premalignant lesions. Notably, compared with transvaginal ultrasonography (TVS) in patients with postmenopausal bleeding, EMPap exhibited superior sensitivity (100% vs. 82.0%) and specificity (85.2% vs. 38.5%). In asymptomatic postmenopausal women, EMPap maintained high sensitivity (89.5%) and negative predictive value (NPV) (98.3%).

conclusionsThis study demonstrated the potential of EMPap as an effective tool for EC detection. Despite the limited sample size, EMPap showed promise for identifying type II EC and detecting over 50% of premalignant lesions. As a DNA methylation classifier, EMPap can reduce unnecessary uterine interventions and improve diagnosis and outcomes.

Indexed as

DNA MethylationEarly Detection of CancerEndometrial NeoplasmsAdultAgedBasic Helix-Loop-Helix ProteinsBiomarkers, TumorCohort StudiesFemaleHumansMiddle AgedSensitivity and SpecificityBasic Helix-Loop-Helix ProteinsBiomarkers, Tumorcervical scrapingsearly detectionendometrial cancermethylationtransvaginal ultrasonography

Identifiers

PMID39487683
PMCPMC11530713

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.