Evidence map›Paper›PMID 31306545›Full record

ArticleMolecular oncology2019

Intra-individual variation of circulating tumour DNA in lung cancer patients.

Johanne A Hojbjerg, Anne T Madsen, Hjordis H Schmidt, Steffen F Sorensen, Magnus Stougaard, Peter Meldgaard, Boe S Sorensen

Open access · goldAbstract read
In one paragraph

Article in Molecular oncology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.0field-weighted citation impact, top 29% of its field
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

13 citing papers in PubMed, 17 citations in OpenAlex.

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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

7 authors at 1 institution in 1 country.

Johanne A HojbjergDepartment of Clinical Biochemistry, Aarhus University Hospital, Denmark.ORCID 0000-0002-5604-3451
Anne T MadsenDepartment of Clinical Biochemistry, Aarhus University Hospital, Denmark.ORCID 0000-0001-9146-5943
Hjordis H SchmidtDepartment of Oncology, Aarhus University Hospital, Denmark.
Steffen F SorensenDepartment of Clinical Biochemistry, Aarhus University Hospital, Denmark.
Magnus StougaardDepartment of Pathology, Aarhus University Hospital, Denmark.
Peter MeldgaardDepartment of Oncology, Aarhus University Hospital, Denmark.
Boe S SorensenDepartment of Clinical Biochemistry, Aarhus University Hospital, Denmark.
Aarhus University Hospital · DK

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Circulating tumour DNA (ctDNA) has been increasingly incorporated into the treatment of cancer patients. ctDNA is generally accepted as a powerful diagnostic tool, whereas the utility of ctDNA to monitor disease activity needs to be fully validated. Central to this challenge is the question of whether changes in longitudinal ctDNA measurements reflect disease activity or merely biological variation. Thus, the aim of this study was to explore the intra-individual biological variation of ctDNA in lung cancer patients. We identified tumour-specific mutations using next-generation sequencing. Day-to-day and hour-to-hour variations in plasma concentrations of the mutant allele and wild-type cell-free DNA (cfDNA) were determined using digital PCR. The levels of the mutant alleles varied by as much as 53% from day to day and 27% from hour to hour. cfDNA varied up to 19% from day to day and up to 56% from hour to hour, as determined using digital PCR. Variations were independent of the concentration. Both mutant allele concentrations and wild-type cfDNA concentrations showed considerable intra-individual variation in lung cancer patients with nonprogressive disease. This pronounced biological variation of the circulating DNA should be investigated further to determine whether ctDNA can be used for monitoring cancer activity.

Indexed as

AgedCirculating Tumor DNADNA, NeoplasmFemaleHigh-Throughput Nucleotide SequencingHumansLung NeoplasmsMaleMiddle AgedMutationCirculating Tumor DNADNA, Neoplasmcirculating tumour DNAdigital PCRIntra-individual variationlung cancernext-generation sequencing

Identifiers

PMID31306545
PMCPMC6763781
OpenAlexW2961214489

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.