Evidence map›Paper›PMID 42558787›Full record

ArticleTherapeutic advances in medical oncology2026

Prognostic performance of a novel multiplex circulating tumor DNA assay for lung cancer outcomes.

Peter Hjorth-Hansen, Line Nederby, Cecilie Mondrup Jacobsen, Morten Borg, Ole Hilberg, Sara Witting Christensen Wen, Signe Timm, Torben Frøstrup Hansen, Rikke Fredslund Andersen

Abstract read
In one paragraph

Article in Therapeutic advances in medical oncology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

9 authors.

Peter Hjorth-HansenDepartment of Oncology, Lillebaelt Hospital, University Hospital of Southern Denmark, Vejle, Denmark.ORCID https://orcid.org/0000-0003-0434-8285
Line NederbyDepartment of Biochemistry and Immunology, Vejle Hospital, University Hospital of Southern Denmark, Beriderbakken 4, Vejle DK-7100, Denmark.ORCID https://orcid.org/0000-0002-0101-328X
Cecilie Mondrup JacobsenDepartment of Oncology, Lillebaelt Hospital, University Hospital of Southern Denmark, Vejle, Denmark.
Morten BorgDepartment of Regional Health Research, University of Southern Denmark, Odense, Denmark.
Ole HilbergDepartment of Regional Health Research, University of Southern Denmark, Odense, Denmark.
Sara Witting Christensen WenDepartment of Regional Health Research, University of Southern Denmark, Odense, Denmark.
Signe TimmDepartment of Oncology, Lillebaelt Hospital, University Hospital of Southern Denmark, Vejle, Denmark.
Torben Frøstrup HansenDepartment of Oncology, Lillebaelt Hospital, University Hospital of Southern Denmark, Vejle, Denmark.
Rikke Fredslund AndersenDepartment of Oncology, Lillebaelt Hospital, University Hospital of Southern Denmark, Vejle, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Lung cancer is a heterogeneous disease with unpredictable trajectories. Risk stratification in lung cancer remains imprecise within tumor-node-metastasis (TNM) stages. Objectives: This work aims to evaluate whether methylated circulating tumor DNA (ctDNA) can improve prognostication at the time of diagnosis. Methods: We enrolled 213 participants with recently diagnosed lung cancer, of whom 100 underwent curative treatment and 113 underwent palliative treatment. All blood samples were collected prior to lung cancer diagnosis and analyzed using multiplex methylation-specific digital droplet polymerase chain reaction targeting five methylated ctDNA markers. ctDNA output was interpreted in two models: a three-tiered (negative/Low-level/High-level ctDNA) and a binary (negative/positive). Results: We observed significantly increased overall survival (OS) among all participants with negative or low-level ctDNA results compared with those with high-level ctDNA. The adjusted hazard ratio (HR) for OS was higher when comparing high-level ctDNA to negative results (HR = 1.96, 95% confidence interval (CI): 1.09-3.51; Conclusion: Detection of, and risk stratification based on, levels of methylated ctDNA at diagnosis appears to provide valuable prognostic information in lung cancer, both in early and late stages of the disease. Such information may have implications for the choice of follow-up regimens and treatment strategies. Design: Retrospective observational cohort study using prospectively collected blood samples.

Indexed as

ctDNAddPCRliquid biopsylung cancermultiplexprognosis

Identifiers

PMID42558787
PMCPMC13438331

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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.