Active Ratio Test (ART) as a Novel Diagnostic for Ovarian Cancer.

Active Ratio Test CXCL10 ELISA biomarkers early detection ovarian cancer

Journal

Diagnostics (Basel, Switzerland)
ISSN: 2075-4418
Titre abrégé: Diagnostics (Basel)
Pays: Switzerland
ID NLM: 101658402

Informations de publication

Date de publication:
07 Jun 2021
Historique:
received: 13 05 2021
revised: 04 06 2021
accepted: 04 06 2021
entrez: 2 7 2021
pubmed: 3 7 2021
medline: 3 7 2021
Statut: epublish

Résumé

Despite substantial effort, there remains a lack of biomarker-based, clinically relevant testing for the accurate, non-invasive diagnostic or prognostic profiling of epithelial ovarian cancers (EOC). Our previous work demonstrated that whilst the inflammatory marker C-X-C motif chemokine ligand 10 (CXCL10) has prognostic relevance in ovarian cancer, its use is complicated by the presence of multiple, N-terminally modified variants, mediated by several enzymes including Dipeptidyl Peptidase 4 (DPP4). In this study, we provide the first evidence for the "Active Ratio Test" (ART) as a novel method to measure biologically relevant CXCL10 proteoforms in clinical samples. In a cohort of 275 patients, ART accurately differentiated patients with malignant EOCs from those with benign gynaecological conditions (AUC 0.8617) and significantly out-performed CA125 alone. Moreover, ART combined with the measurement of CA125 and DPP4 significantly increased prognostic performance (AUC 0.9511; sensitivity 90.0%; specificity 91.7%; Cohen's d > 1) for EOC detection. Our data demonstrate that ART provides a useful method to accurately discriminate between patients with benign versus malignant EOC, and highlights their relevance to ovarian cancer diagnosis. This marker combination may also be applicable in broader screening applications, to identify or discriminate benign from malignant disease in asymptomatic women.

Sections du résumé

BACKGROUND BACKGROUND
Despite substantial effort, there remains a lack of biomarker-based, clinically relevant testing for the accurate, non-invasive diagnostic or prognostic profiling of epithelial ovarian cancers (EOC). Our previous work demonstrated that whilst the inflammatory marker C-X-C motif chemokine ligand 10 (CXCL10) has prognostic relevance in ovarian cancer, its use is complicated by the presence of multiple, N-terminally modified variants, mediated by several enzymes including Dipeptidyl Peptidase 4 (DPP4).
METHODS METHODS
In this study, we provide the first evidence for the "Active Ratio Test" (ART) as a novel method to measure biologically relevant CXCL10 proteoforms in clinical samples.
RESULTS RESULTS
In a cohort of 275 patients, ART accurately differentiated patients with malignant EOCs from those with benign gynaecological conditions (AUC 0.8617) and significantly out-performed CA125 alone. Moreover, ART combined with the measurement of CA125 and DPP4 significantly increased prognostic performance (AUC 0.9511; sensitivity 90.0%; specificity 91.7%; Cohen's d > 1) for EOC detection.
CONCLUSION CONCLUSIONS
Our data demonstrate that ART provides a useful method to accurately discriminate between patients with benign versus malignant EOC, and highlights their relevance to ovarian cancer diagnosis. This marker combination may also be applicable in broader screening applications, to identify or discriminate benign from malignant disease in asymptomatic women.

Identifiants

pubmed: 34200333
pii: diagnostics11061048
doi: 10.3390/diagnostics11061048
pmc: PMC8230042
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Ovarian Cancer Research Foundation
ID : GA-2018-11

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Auteurs

Sung-Woog Kang (SW)

Hudson Institute of Medical Research, Clayton 3168, Australia.
Department of Molecular and Translational Sciences, Monash University, Clayton 3168, Australia.

Adam Rainczuk (A)

Hudson Institute of Medical Research, Clayton 3168, Australia.
Department of Molecular and Translational Sciences, Monash University, Clayton 3168, Australia.
Bruker Pty Ltd., Preston 3072, Australia.

Martin K Oehler (MK)

Department of Gynaecological Oncology, Royal Adelaide Hospital, Adelaide 5000, Australia.
Robinson Institute, University of Adelaide, Adelaide 5000, Australia.

Thomas W Jobling (TW)

Department of Gynaecology Oncology, Monash Medical Centre, Bentleigh East 3165, Australia.

Magdalena Plebanski (M)

School of Health and Biomedical Sciences, RMIT University, Bundoora 3083, Australia.

Andrew N Stephens (AN)

Hudson Institute of Medical Research, Clayton 3168, Australia.
Department of Molecular and Translational Sciences, Monash University, Clayton 3168, Australia.

Classifications MeSH