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


Journal

BMC cancer
ISSN: 1471-2407
Titre abrégé: BMC Cancer
Pays: England
ID NLM: 100967800

Informations de publication

Date de publication:
30 Jul 2022
Historique:
received: 15 11 2021
accepted: 06 07 2022
entrez: 30 7 2022
pubmed: 31 7 2022
medline: 3 8 2022
Statut: epublish

Résumé

To 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. This 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). Of 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. ROMA 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.

Sections du résumé

BACKGROUND BACKGROUND
To 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.
METHODS METHODS
This 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).
RESULTS RESULTS
Of 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.
CONCLUSIONS CONCLUSIONS
ROMA 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.

Identifiants

pubmed: 35907794
doi: 10.1186/s12885-022-09887-5
pii: 10.1186/s12885-022-09887-5
pmc: PMC9338568
doi:

Substances chimiques

Biomarkers, Tumor 0
CA-125 Antigen 0
Proteins 0
WAP Four-Disulfide Core Domain Protein 2 0
WFDC2 protein, human 0

Types de publication

Journal Article Multicenter Study Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

831

Informations de copyright

© 2022. The Author(s).

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Auteurs

Elena Ioana Braicu (EI)

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.
Department of Obstetrics and Gynecology, Stanford University, California, USA. elena.braicu@charite.de.

Catherine Linn Krause (CL)

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 Torsten (U)

Department for Gynecology, Vivantes Klinikum Neukölln, Berlin, Germany.

Herbert Mecke (H)

Department for Obstetrics and Gynecology, AVK Vivantes, Berlin, Germany.

Rolf Richter (R)

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.

Lars Hellmeyer (L)

Department for Obstetrics and Gynecolgy, Vivantes Klinikum Friedrichshain, Berlin, Germany.

Malgorzata Lanowska (M)

Department of Gynecology, Charité - Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Campus Charité Mitte, Berlin, Germany.

Bodo Müller (B)

Department for Gynecology, Vivantes Klinikum Kaulsdorf, Berlin, Germany.

Elisa Koch (E)

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.

Janine Boenneß-Zaloum (J)

Department for Obstetrics and Gynecolgy, Vivantes Klinikum Friedrichshain, Berlin, Germany.

Kerstin Ames (K)

Department for Gynecology, Vivantes Klinikum Neukölln, Berlin, Germany.

Radoslav Chekerov (R)

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.

Kati Hasenbein (K)

Department for Gynecology, Vivantes Klinikum Humboldthain, Berlin, Germany.

Mathias Zimmermann (M)

Central Institute of Laboratory Medicine, DRK Kliniken Berlin, Berlin, Germany.

Mandy Mangler (M)

Department of Gynecology, Charité - Universitätsmedizin Berlin, Freie Universität Berlin, Humboldt-Universität zu Berlin, and Berlin Institute of Health, Campus Charité Mitte, Berlin, Germany.

Frank Chen (F)

Department for Obstetrics and Gynecology, AVK Vivantes, Berlin, Germany.

Rudolf Tauber (R)

Charité - 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 Sehouli (J)

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.

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