Evidence map›Paper›PMID 34151844›Full record

ArticleCancer biomarkers : section A of Disease markers2021

Clinical value of tumor-associated antigens and autoantibody panel combination detection in the early diagnostic of lung cancer.

Renren Ouyang, Shiji Wu, Bo Zhang, Ting Wang, Botao Yin, Jin Huang, Wei Wei, Min Huang, Minxia Zhang, Yun Wang and 2 more

Abstract read
In one paragraph

Article in Cancer biomarkers : section A of Disease markers, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

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0cells of the map it votes in
11citing papers in PubMed
–field-weighted citation impact
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

Who cites it

11 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Renren Ouyang
Shiji Wu
Bo Zhang
Ting Wang
Botao Yin
Jin Huang
Wei Wei
Min Huang
Minxia Zhang
Yun Wang
Feng Wang
Hongyan Hou

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThis study aimed to investigate the efficiency of combining tumor-associated antigens (TAAs) and autoantibodies in the diagnosis of lung cancer.

methodsThe serum levels of TAAs and seven autoantibodies (7-AABs) were detected from patients with lung cancer, benign lung disease and healthy controls. The performance of a new panel by combing TAAs and 7-AABs was evaluated for the early diagnosis of lung cancer.

resultsThe positive rate of 7-AABs was higher than the single detection of antibody. The positive rate of the combined detection of 7-AABs in lung cancer group (30.2%) was significantly higher than that of healthy controls (16.8%), but had no statistical difference compared with that of benign lung disease group (20.8%). The positive rate of 7-AABs showed a tendency to increase in lung cancer patients with higher tumor-node-metastasis (TNM) stages. For the pathological subtype analysis, the positive rate of 7-AABs was higher in patients with squamous cell carcinoma and small cell lung cancer than that of adenocarcinoma. The levels of carcinoembryonic antigen (CEA) and cytokeratin 19 fragment 211 (CYFRA 21-1) were significantly higher than that of benign lung disease and healthy control groups. An optimal model was established (including 7-AABs, CEA and CYFRA21-1) to distinguish lung cancer from control groups. The performance of this model was superior than that of single markers, with a sensitivity of 52.26% and specificity of 77.46% in the training group. Further assessment was studied in another validation group, with a sensitivity of 44.02% and specificity of 83%.

conclusionsThe diagnostic performance was enhanced by combining 7-AABs, CEA and CYFRA21-1, which has critical value for the screening and early detection of lung cancer.

Indexed as

AutoantibodiesEpithelial Cell Adhesion MoleculeFemaleHumansLung NeoplasmsMaleMiddle AgedRetrospective StudiesAutoantibodiesEpithelial Cell Adhesion MoleculeCEACYFRA 21-1Lung cancertumor-associated antigentumor-associated autoantibodies

Identifiers

PMID34151844
PMCPMC12500059

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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.