Evidence map›Paper›PMID 39682108›Full record

ReviewCancers2024

Circulating Tumor DNA in Early and Metastatic Breast Cance-Current Role and What Is Coming Next.

Christian Martin Tegeler, Andreas Daniel Hartkopf, Maggie Banys-Paluchowski, Natalia Krawczyk, Tanja Fehm, Bernadette Anna Sophia Jaeger

Abstract readReview
In one paragraph

Review in Cancers, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
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  6. Review
  7. 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

6 authors.

Christian Martin TegelerDepartment of Obstetrics and Gynecology, University Hospital Tübingen, 72076 Tübingen, Germany.ORCID 0000-0001-6688-7351
Andreas Daniel HartkopfDepartment of Obstetrics and Gynecology, University Hospital Tübingen, 72076 Tübingen, Germany.ORCID 0000-0003-1227-1118
Maggie Banys-PaluchowskiDepartment of Gynecology and Obstetrics, University Hospital Schleswig-Holstein, Campus Luebeck, 23538 Luebeck, Germany.
Natalia KrawczykDepartment of Gynecology and Obstetrics, University Hospital Düsseldorf, 40225 Duesseldorf, Germany.ORCID 0000-0003-0319-486X
Tanja FehmDepartment of Gynecology and Obstetrics, University Hospital Düsseldorf, 40225 Duesseldorf, Germany.
Bernadette Anna Sophia JaegerDepartment of Gynecology and Obstetrics, University Hospital Düsseldorf, 40225 Duesseldorf, Germany.ORCID 0000-0002-7861-7276

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The progress that has been made in recent years in relation to liquid biopsies in general and circulating tumor DNA (ctDNA) in particular can be seen as groundbreaking for the future of breast cancer treatment, monitoring and early detection. Cell-free DNA (cfDNA) consists of circulating DNA fragments released by various cell types into the bloodstream. A portion of this cfDNA, known as ctDNA, originates from malignant cells and carries specific genetic mutations. Analysis of ctDNA provides a minimally invasive method for diagnosis, monitoring response to therapy, and detecting the emergence of resistance. Several methods are available for the analysis of ctDNA, each with distinct advantages and limitations. Quantitative polymerase chain reaction is a well-established technique widely used due to its high sensitivity and specificity, particularly for detecting known mutations. In addition to the detection of individual mutations, multigene analyses were developed that could detect several mutations at once, including rarer mutations. These methods are complementary and can be used strategically depending on the clinical question. In the context of metastatic breast cancer, ctDNA holds particular promise as it allows for the dynamic monitoring of tumor evolution. Through ctDNA analysis, mutations in the

Indexed as

ctDNAearly breast cancerliquid biopsymetastatic breast cancerpredictive markerprognostic marker

Identifiers

PMID39682108
PMCPMC11640659

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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.