Evidence map›Paper›PMID 36404535›Full record

ArticleCancer biomarkers : section A of Disease markers2023

Assessment of circulating biomarkers for detection of lung cancer in a high-risk cohort.

Morten Borg, Line Nederby, Sara Witting Christensen Wen, Torben Frøstrup Hansen, Anders Jakobsen, Rikke Fredslund Andersen, Ulla Møller Weinreich, Ole Hilberg

Abstract read
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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

2 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Biomarkers Suitable for Early Detection of Intrathoracic Cancers in Primary Care: A Systematic Review.Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology · 2025
    Pooled it
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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

8 authors.

Morten BorgDepartment of Respiratory Diseases, Aalborg University Hospital, Aalborg, Denmark.
Line NederbyDepartment of Clinical Biochemistry, Lillebaelt Hospital, Vejle, Denmark.
Sara Witting Christensen WenDepartment of Oncology, Lillebaelt Hospital, Vejle, Denmark.
Torben Frøstrup HansenDepartment of Oncology, Lillebaelt Hospital, Vejle, Denmark.
Anders JakobsenDepartment of Oncology, Lillebaelt Hospital, Vejle, Denmark.
Rikke Fredslund AndersenDepartment of Clinical Biochemistry, Lillebaelt Hospital, Vejle, Denmark.
Ulla Møller WeinreichDepartment of Respiratory Diseases, Aalborg University Hospital, Aalborg, Denmark.
Ole HilbergDepartment of Internal Medicine, Lillebaelt Hospital, Vejle, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThere is an urgent need for early detection of lung cancer. Screening with low-dose computed tomography (LDCT) is now implemented in the US. Supplementary use of a lung cancer biomarker with high specificity is desirable.

objectiveTo assess the diagnostic properties of a biomarker panel consisting of cytokeratin 19 fragment (CYFRA 21-1), carcinoembryonic antigen (CEA) and cancer antigen 125 (CA125).

methodsA cohort of 250 high-risk patients was investigated on suspicion of lung cancer. Ahead of diagnostic work-up, blood samples taken. Cross-validated prediction models were computed to assess lung cancer detection properties.

resultsIn total 32% (79/250) of patients were diagnosed with lung cancer. Area under the curve (AUC) for the three biomarkers was of 0.795, with sensitivity/specificity of 57%/93% and negative predictive value of 83%. When combining the biomarkers with US screening criteria, the AUC was 0.809, while applying only US screening criteria on the cohort, yielded an AUC of 0.62. The ability of the biomarkers to detect stage I-II lung cancer was substantially lower; AUC 0.54.

conclusionsIn a high-risk cohort, the detection properties of the three biomarkers were acceptable compared to current LDCT screening criteria. However, the ability to detect early stage lung cancer was low.

Indexed as

Lung NeoplasmsAntigens, NeoplasmArea Under CurveBiomarkers, TumorCarcinoembryonic AntigenHumansKeratin-19antigen CYFRA21.1Antigens, NeoplasmBiomarkers, TumorCarcinoembryonic AntigenKeratin-19biomarkerscancer antigen 125 (CA125)carcinoembryonic antigen (CEA)cytokeratin 19 fragment (CYFRA 21-1)Lung cancerscreening

Identifiers

PMID36404535
PMCPMC12412793

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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.