Evidence map›Paper›PMID 29356357›Full record

ArticleCancer medicine2018

CTAPIII/CXCL7: a novel biomarker for early diagnosis of lung cancer.

Qiang Du, Encheng Li, Yonge Liu, Wenli Xie, Chun Huang, Jiaqi Song, Wei Zhang, Yijie Zheng, Huiling Wang, Qi Wang

Open access · goldAbstract read
In one paragraph

Article in Cancer medicine, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.7field-weighted citation impact, top 7% 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

22 citing papers in PubMed, 35 citations in OpenAlex.

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  7. Ginsenoside Rg1 Suppresses Non-Small-Cell Lung Cancer via MicroRNA-126-PI3K-AKT-mTOR Pathway.Evidence-based complementary and alternative medicine : eCAM · 2022
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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

10 authors at 5 institutions in 1 country.

Qiang DuDepartment of Respiratory Medicine, The Second Affiliated Hospital, Dalian Medical University, Dalian, China.ORCID 0000-0002-5033-6405
Encheng LiDepartment of Respiratory Medicine, The Second Affiliated Hospital, Dalian Medical University, Dalian, China.
Yonge LiuDepartment of Clinical Laboratory, The Second Affiliated Hospital, Dalian Medical University, Dalian, China.
Wenli XieDepartment of Cardiology Medicine, The Second Affiliated Hospital, Dalian Medical University, Dalian, China.
Chun HuangDepartment of Respiratory Medicine, The North Area of Suzhou Municipal Hospital, Suzhou, China.
Jiaqi SongDepartment of Health Statistics, Second Military Medical University, Shanghai, China.
Wei ZhangDepartment of Biostatistics, School of Public Health, Fudan University, Shanghai, China.
Yijie ZhengMedical Scientific Liaison Asian Pacific, Abbott Diagnostics Division, Abbott Laboratories, Shanghai, China.
Huiling WangDepartment of Respiratory Medicine, The Second Affiliated Hospital, Dalian Medical University, Dalian, China.
Qi WangDepartment of Respiratory Medicine, The Second Affiliated Hospital, Dalian Medical University, Dalian, China.
Dalian Medical University · CNAbbott (China) · CNFudan University · CNSecond Military Medical University · CNSuzhou Municipal Hospital · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

It is desirable to have a biomarker which can facilitate low-dose CT in diagnosis of early stage lung cancer. CTAPIII/CXCL7 is reported to be a potential biomarker for diagnosis of early lung cancer. In this study, we investigated the serum level of CTAPIII/CXCL7 in patients at different stage of lung cancer and the diagnostic efficacy of CTAPIII/CXCL7 in NSCLC. The plasma level of CTAPIII/CXCL7 was assayed by ELISA. CEA, SCCAg, and Cyfra211 were measured using a commercial chemiluminescent microparticle immunoassay. A total of 419 subjects were recruited, including 265 NSCLC patients and 154 healthy individuals. The subjects were randomly assigned to a training set and a test set. Receiver operating characteristic (ROC) and binary logistic regression analyses were conducted to evaluate the diagnostic efficacy and establish diagnostic mathematical model. Plasma CTAPIII/CXCL7 levels were significantly higher in NSCLC patients than in controls, which was independent of the stage of NSCLC. The diagnostic efficiency of CTAPIII/CXCL7 in NSCLC (training set: area under ROC curve (AUC) 0.806, 95% CI: 0.748-0.863; test set: AUC 0.773, 95% CI: 0.711-0.835) was greater than that of SCCAg, Cyfra21-1, or CEA. The model combining CTAPIII/CXCL7 with CEA, SCCAg, and Cyfra21-1 was more effective for NSCLC diagnosis than CTAPIII/CXCL7 alone. In addition, plasma level of CTAPIII/CXCL7 may contribute to the early diagnosis of NSCLC. CTAPIII/CXCL7 can be used as a plasma biomarker for the diagnosis of NSCLCs, particularly early stage lung cancer, with relatively high sensitivity and specificity.

Indexed as

AdultAgedAged, 80 and overbeta-ThromboglobulinBiomarkers, TumorCarcinoma, Non-Small-Cell LungCase-Control StudiesEarly Detection of CancerFemaleFollow-Up StudiesHumansLung NeoplasmsMaleMiddle AgedPrognosisROC Curvebeta-ThromboglobulinBiomarkers, TumorPPBP protein, humanEarly diagnosislung cancerserum biomarkers

Identifiers

PMID29356357
PMCPMC5806116
OpenAlexW2791184597

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.