Evidence map›Paper›PMID 35907794›Full record

Observational studyBMC cancer2022

HE4 as a serum biomarker for the diagnosis of pelvic masses: a prospective, multicenter study in 965 patients.

Elena Ioana Braicu, Catherine Linn Krause, Uwe Torsten, Herbert Mecke, Rolf Richter, Lars Hellmeyer, Malgorzata Lanowska, Bodo Müller, Elisa Koch, Janine Boenneß-Zaloum and 8 more

Open access · goldAbstract readMulticenter StudyObservational Study
In one paragraph

Observational study in BMC cancer, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
3.9field-weighted citation impact, top 6% 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

14 citing papers in PubMed, 21 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

18 authors at 6 institutions in 1 country.

Elena Ioana Braicu *Department of Gynecology with Center of Oncological Surgery, Charité - Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Campus Virchow Klinikum, Augustenburger Platz 1, 13353, Berlin, Germany. elena.braicu@charite.de.
Catherine Linn Krause *Department of Gynecology with Center of Oncological Surgery, Charité - Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Campus Virchow Klinikum, Augustenburger Platz 1, 13353, Berlin, Germany.
Uwe TorstenDepartment for Gynecology, Vivantes Klinikum Neukölln, Berlin, Germany.
Herbert MeckeDepartment for Obstetrics and Gynecology, AVK Vivantes, Berlin, Germany.
Rolf RichterDepartment of Gynecology with Center of Oncological Surgery, Charité - Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Campus Virchow Klinikum, Augustenburger Platz 1, 13353, Berlin, Germany.
Lars HellmeyerDepartment for Obstetrics and Gynecolgy, Vivantes Klinikum Friedrichshain, Berlin, Germany.
Malgorzata LanowskaDepartment of Gynecology, Charité - Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Campus Charité Mitte, Berlin, Germany.
Bodo MüllerDepartment for Gynecology, Vivantes Klinikum Kaulsdorf, Berlin, Germany.
Elisa KochDepartment of Gynecology with Center of Oncological Surgery, Charité - Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Campus Virchow Klinikum, Augustenburger Platz 1, 13353, Berlin, Germany.
Janine Boenneß-ZaloumDepartment for Obstetrics and Gynecolgy, Vivantes Klinikum Friedrichshain, Berlin, Germany.
Kerstin AmesDepartment for Gynecology, Vivantes Klinikum Neukölln, Berlin, Germany.
Radoslav ChekerovDepartment of Gynecology with Center of Oncological Surgery, Charité - Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Campus Virchow Klinikum, Augustenburger Platz 1, 13353, Berlin, Germany.
Kati HasenbeinDepartment for Gynecology, Vivantes Klinikum Humboldthain, Berlin, Germany.
Mathias ZimmermannCentral Institute of Laboratory Medicine, DRK Kliniken Berlin, Berlin, Germany.
Mandy ManglerDepartment of Gynecology, Charité - Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Campus Charité Mitte, Berlin, Germany.
Frank ChenDepartment for Obstetrics and Gynecology, AVK Vivantes, Berlin, Germany.
Rudolf TauberCharité - Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Institute of Laboratory Medicine, Clinical Chemistry and Pathobiochemistry and Labor Berlin Charité, Berlin, Germany.
Jalid SehouliDepartment of Gynecology with Center of Oncological Surgery, Charité - Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Campus Virchow Klinikum, Augustenburger Platz 1, 13353, Berlin, Germany.
Vivantes Klinikum · DECharité - Universitätsmedizin Berlin · DEFreie Universität Berlin · DEHumboldt-Universität zu Berlin · DEKlinikum im Friedrichshain · DEDRK Kliniken Berlin · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTo evaluate the diagnostic value of adding human epididymis protein 4 (HE4), cancer antigen 125 (CA125) and risk of malignancy algorithm (ROMA) to ultrasound for detecting ovarian cancer in patients with a pelvic mass.

methodsThis was a prospective, observational, multicenter study. Patients aged > 18 years who were scheduled to undergo surgery for a suspicious pelvic mass had CA125 and HE4 levels measured prior to surgery, in addition to a routine transvaginal ultrasound scan. The diagnostic performance of CA125, HE4 and ROMA for distinguishing between benign and malignant adnexal masses was assessed using receiver operating characteristic (ROC) analysis and the corresponding area under the curve (AUC).

resultsOf 965 evaluable patients, 804 were diagnosed with benign tumors and 161 were diagnosed with ovarian cancer. In late-stage ovarian cancer, CA125, HE4 and ROMA all had an excellent diagnostic performance (AUC > 0.92), whereas in stage I and II, diagnostic performance of all three biomarkers was less adequate (AUC < 0.77). In the differential diagnosis of ovarian cancer and endometriosis, ROMA and HE4 performed better than CA125 with 99 and 98.1% versus 75.0% sensitivity, respectively, at 75.4% specificity.

conclusionsROMA and HE4 could be valuable biomarkers to help with the diagnosis of ovarian cancer in premenopausal patients in order to differentiate from endometriosis, whereas CA125 may be more adequate for postmenopausal patients.

Indexed as

EndometriosisOvarian NeoplasmsAlgorithmsBiomarkers, TumorCA-125 AntigenCarcinoma, Ovarian EpithelialFemaleHumansProspective StudiesProteinsROC CurveWAP Four-Disulfide Core Domain Protein 2Biomarkers, TumorCA-125 AntigenProteinsWAP Four-Disulfide Core Domain Protein 2WFDC2 protein, humanBiomarkersCA125EndometriosisHE4Ovarian cancer

Identifiers

PMID35907794
PMCPMC9338568
OpenAlexW4288684415

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.