Evidence map›Paper›PMID 42804029›Full record

SynthesisBreast cancer research and treatment2026

Circulating tumour DNA and its clinical relevance in predicting progression-free survival and overall survival in patients with advanced breast cancer: a systematic review and meta-analysis.

Cæcilie Ottosen, Ea Kragelund, Mette Abildgaard Pedersen, Vivi Quoc Nguyen, Sakina Kousgaard Khan, Helene Borup Larsen, Anders Lerche Møller, Sofie Høier Gamborg-Kvist, Karen-Lise Garm Spindler, Anne Sofie Brems-Eskildsen and 1 more

Abstract readSystematic ReviewMeta-Analysis
PubMed Publisher
In one paragraph

Synthesis in Breast cancer research and treatment, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Cæcilie Ottosen *Department of Oncology, Aarhus University Hospital, Aarhus, Denmark. caeott@rm.dk.ORCID http://orcid.org/0000-0002-1606-2885
Ea Kragelund *Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.
Mette Abildgaard PedersenDepartment of Pathology, Aarhus University Hospital, Aarhus, Denmark.
Vivi Quoc NguyenDepartment of Oncology, Aarhus University Hospital, Aarhus, Denmark.
Sakina Kousgaard KhanDepartment of Oncology, Aarhus University Hospital, Aarhus, Denmark.
Helene Borup LarsenDepartment of Oncology, Aarhus University Hospital, Aarhus, Denmark.
Anders Lerche MøllerDepartment of Oncology, Aarhus University Hospital, Aarhus, Denmark.
Sofie Høier Gamborg-KvistDepartment of Oncology, Lillebaelt Hospital, Vejle, Denmark.
Karen-Lise Garm SpindlerDepartment of Oncology, Aarhus University Hospital, Aarhus, Denmark.
Anne Sofie Brems-Eskildsen *Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.
Louise Bach Callesen *Department of Oncology, Aarhus University Hospital, Aarhus, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeTreatment strategies for advanced breast cancer (ABC) are rapidly evolving, but treatment decisions and monitoring remain dependent on imaging-based assessments. Circulating tumour DNA (ctDNA) has emerged as a minimally invasive biomarker with potential to provide real-time assessments, yet its clinical relevance in ABC has not been established. This systematic review and meta-analysis evaluates the prognostic value of ctDNA in ABC.

methodsMedline, Embase, and Cochrane databases were systematically searched up to 07/02/2025. Eligible studies analysed associations between ctDNA and progression free survival (PFS) and/or overall survival (OS) in patient with ABC. Study quality was assessed using the Quality in Prognosis Studies Tool. Hazard ratios (HR) with 95% confidence intervals (CI) were extracted, and meta-analyses were performed using random-effects models.

resultsSixty-four studies were included and divided into subgroups. Elevated ctDNA levels at baseline were significantly associated with shorter PFS (n = 2,586, pooled HR = 2.0; 95% CI: 1.8-2.3) and OS (n = 2,454, pooled HR = 2.6; 95% CI: 2.1-3.3). Unfavourable changes in ctDNA levels were associated with reduced PFS (n = 710, pooled HR = 2.5; 95% CI: 1.9-3.4) and OS (n = 154, pooled HR = 2.4; 95% CI: 1.5-3.8). Additionally, analyses on specific genetic alterations in ctDNA and survival outcomes indicated a less favourable prognosis when detected at baseline. However, results were not consistent.

conclusionsThis review supports an association between baseline ctDNA levels, on-treatment changes in ctDNA levels, and survival outcomes in ABC. Furthermore, specific genetic alterations in ctDNA add prognostic information and may support treatment tailoring.

trial registrationRegistered in PROSPERO (CRD42024534851).

Indexed as

Biomarkers, TumorBreast NeoplasmsCirculating Tumor DNAFemaleHumansPrognosisProgression-Free SurvivalBiomarkers, TumorCirculating Tumor DNAAdvanced breast cancerCirculating tumour DNActDNActDNA-RECISTctDNA response evaluation criteria in solid tumoursSystematic review

Identifiers

PMID42804029

What OpenQuestion holds

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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.