Evidence map›Paper›PMID 41602395›Full record

ReviewFrontiers in oncology2025

The role of circulating tumor DNA in gynecological cancer management.

Min Gao, Pei-Yan Yu, Run-Xuan Li, Chen Chen, Xiao-Feng Cong, Zi-Ling Liu

Abstract readReview
In one paragraph

Review in Frontiers in oncology, 2025. 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

6 authors.

Min GaoCancer Center, the First Hospital of Jilin University, Changchun, Jilin, China.
Pei-Yan YuCancer Center, the First Hospital of Jilin University, Changchun, Jilin, China.
Run-Xuan LiCancer Center, the First Hospital of Jilin University, Changchun, Jilin, China.
Chen ChenCancer Center, the First Hospital of Jilin University, Changchun, Jilin, China.
Xiao-Feng CongCancer Center, the First Hospital of Jilin University, Changchun, Jilin, China.
Zi-Ling LiuCancer Center, the First Hospital of Jilin University, Changchun, Jilin, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ovarian cancer, endometrial cancer, and cervical cancer represent the three most prevalent primary gynecological tumors that pose a significant threat to women's health globally. To enhance survival rates for patients with gynecological cancers, there is an urgent need to optimize disease detection and monitoring technologies aimed at improving early diagnosis, treatment efficacy monitoring, treatment guidance, and prognosis prediction. Currently, traditional methods for identifying and tracking malignant tumors primarily depend on imaging studies, supplemented by blood-based protein biomarker testing. However, these biomarkers generally exhibit limitations in terms of sensitivity and specificity. Circulating tumor DNA (ctDNA), comprising DNA fragments released by cancer cells into the bloodstream, can be detected using liquid biopsy technology. Compared to tissue biopsy, ctDNA testing offers the advantages of minimal invasiveness and continuous monitoring, thereby eliminating the need for multiple surgeries. In addition, it may detect disease recurrence or predict behavior in ways that entity organization biopsy, tumor marker monitoring, and imaging cannot. Increasing evidence indicates that ctDNA has the potential to enhance the clinical management of gynecological tumors by improving early diagnosis, monitoring treatment responses, detecting recurrences, and predicting prognosis. This review aims to summarize the application of ctDNA in gynecological cancers and provide an overview of its comprehensive research and clinical validation. Furthermore, we discuss future development directions based on existing challenges and identify areas requiring further research to elucidate the potential of ctDNA in clinical applications.

Indexed as

circulating tumor DNAgynecological cancernext-generation sequencingpolymerase chain reactionprecision oncology

Identifiers

PMID41602395
PMCPMC12832360

What OpenQuestion holds

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LicenceCC BY
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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.