Evidence map›Paper›PMID 25935153›Full record

ArticleJournal of ovarian research2015

M-CSF in a new biomarker panel with HE4 and CA 125 in the diagnostics of epithelial ovarian cancer patients.

Grażyna Ewa Będkowska, Sławomir Ławicki, Ewa Gacuta, Przemysław Pawłowski, Maciej Szmitkowski

Open access · goldAbstract read
In one paragraph

Article in Journal of ovarian research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
4.2field-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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 29 citations in OpenAlex.

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  11. Elevated OGN expression correlates with the EMT signature and poor prognosis in ovarian carcinoma.International journal of clinical and experimental pathology · 2019
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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

5 authors at 1 institution in 1 country.

Grażyna Ewa BędkowskaDepartment of Haematological Diagnostics, Medical University, Białystok, Poland. grazyna.bedkowska@umb.edu.pl.
Sławomir ŁawickiDepartment of Biochemical Diagnostics, Medical University Białystok, Waszyngtona 15A, Białystok, 15-269, Poland. slawicki@umb.edu.pl.
Ewa GacutaDepartment of Perinatology, Medical University, Białystok, Poland. sunnyeve@wp.pl.
Przemysław PawłowskiDepartment of Pediatric Ophthalmology with Squint Treatment Unit, Medical University, Białystok, Poland. przem38@wp.pl.
Maciej SzmitkowskiDepartment of Biochemical Diagnostics, Medical University Białystok, Waszyngtona 15A, Białystok, 15-269, Poland. zdb@umwb.edu.pl.
Medical University of Białystok · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundWe investigated plasma levels of M-CSF and conventional tumor markers (HE4 and CA 125) in epithelial ovarian cancer patients as compared to control groups: benign ovarian tumor patients (cysts) and healthy subjects.

methodsM-CSF levels were determined by ELISA, HE4 and CA 125 levels - by CMIA method.

resultsOur results have demonstrated significant differences in the concentration levels of M-CSF, CA 125 and HE4 between the groups of ovarian cancer patients, cysts patients and the healthy controls. In the groups tested M-CSF demonstrated equal to or higher values than both CA 125 and HE4 in diagnostic sensitivity (SE), positive and negative predictive values (PPV, NPV), and in the area under the ROC curve (AUC), particularly in the group with the serous epithelial sub-type of OC. Moreover, CA 125 showed better results of the aforementioned diagnostic criteria than HE4. The combined use of the parameters studied resulted in a further, significant increase in the value of the diagnostic indicators and in the value of the diagnostic power (AUC), especially in the early stages of ovarian cancer.

conclusionsThese findings suggest a high usefulness of M-CSF in diagnosing the serous sub-type of epithelial ovarian cancer and in discriminating between cancer and non-carcinoma lesions, particularly in new diagnostic panels in combination with CA 125 and HE4 for the detection of EOC in the early stages.

Indexed as

AgedAged, 80 and overArea Under CurveBiomarkers, TumorCA-125 AntigenCarcinoma, Ovarian EpithelialEnzyme-Linked Immunosorbent AssayFemaleHumansLuminescent MeasurementsMacrophage Colony-Stimulating FactorMiddle AgedNeoplasms, Glandular and EpithelialOvarian NeoplasmsProteinsROC CurveBiomarkers, TumorCA-125 AntigenMacrophage Colony-Stimulating FactorProteinsWAP Four-Disulfide Core Domain Protein 2WFDC2 protein, human

Identifiers

PMID25935153
PMCPMC4426179
OpenAlexW2114796219

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.