A Novel Two-Lipid Signature Is a Strong and Independent Prognostic Factor in Ovarian Cancer.

biomarker ceramide lipid lipidomics outcome ovarian cancer patient stratification personalized medicine phospholipid plasmalogen prognosis

Journal

Cancers
ISSN: 2072-6694
Titre abrégé: Cancers (Basel)
Pays: Switzerland
ID NLM: 101526829

Informations de publication

Date de publication:
07 Apr 2021
Historique:
received: 23 02 2021
revised: 30 03 2021
accepted: 03 04 2021
entrez: 30 4 2021
pubmed: 1 5 2021
medline: 1 5 2021
Statut: epublish

Résumé

Epithelial ovarian cancer (EOC) generally responds well to oncological treatments, but the eventual development of a refractory disease is a major clinical problem. Presently, there are no prognostic blood-based biomarkers for the stratification of EOC patients at the time of diagnosis. We set out to assess and validate the prognostic utility of a novel two-lipid signature, as the lipidome is known to be markedly aberrant in EOC patients. The study consisted of 499 women with histologically confirmed EOC that were prospectively recruited at the university hospitals in Turku (Finland) and Charité (Berlin, Germany). Lipidomic screening by tandem liquid chromatography-mass spectrometry (LC-MS/MS) was performed for all baseline serum samples of these patients, and additionally for 20 patients of the Turku cohort at various timepoints. A two-lipid signature, based on the ratio of the ceramide Cer(d18:1/18:0) and phosphatidylcholine PC(O-38:4), showed consistent prognostic performance in all investigated study cohorts. In the Turku cohort, the unadjusted hazard ratios (HRs) per standard deviation (SD) (95% confidence interval) were 1.79 (1.40, 2.29) for overall and 1.40 (1.14, 1.71) for progression-free survival. In a Charité cohort incorporating only stage III completely resected patients, the corresponding HRs were 1.59 (1.08, 2.35) and 1.53 (1.02, 2.30). In linear-mixed models predicting progression of the disease, the two-lipid signature showed higher performance (beta per SD increase 1.99 (1.38, 2.97)) than cancer antigen 125 (CA-125, 1.78 (1.13, 2.87)). The two-lipid signature was able to identify EOC patients with an especially poor prognosis at the time of diagnosis, and also showed promise for the detection of disease relapse.

Identifiants

pubmed: 33917079
pii: cancers13081764
doi: 10.3390/cancers13081764
pmc: PMC8067677
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Liina Salminen (L)

Department of Obstetrics and Gynecology, Turku University Hospital and University of Turku, 20521 Turku, Finland.

Elena Ioana Braicu (EI)

Department of Gynecology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt Universität zu Berlin, and Berlin Institute of Health, Campus Virchow Klinikum, 13353 Berlin, Germany.

Mitja Lääperi (M)

Zora Biosciences Oy, 02150 Espoo, Finland.

Antti Jylhä (A)

Zora Biosciences Oy, 02150 Espoo, Finland.

Sinikka Oksa (S)

Satasairaala Central Hospital, Department of Obstetrics and Gynecology, 28500 Pori, Finland.

Sakari Hietanen (S)

Department of Obstetrics and Gynecology, Turku University Hospital and University of Turku, 20521 Turku, Finland.

Jalid Sehouli (J)

Department of Gynecology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt Universität zu Berlin, and Berlin Institute of Health, Campus Virchow Klinikum, 13353 Berlin, Germany.

Hagen Kulbe (H)

Department of Gynecology, Charité-Universitätsmedizin Berlin, Corporate Member of Freie Universität Berlin, Humboldt Universität zu Berlin, and Berlin Institute of Health, Campus Virchow Klinikum, 13353 Berlin, Germany.

Andreas du Bois (AD)

Department of Gynecology and Gynecologic Oncology, Kliniken Essen-Mitte, 45136 Essen, Germany.

Sven Mahner (S)

Department of Obstetrics and Gynecology, University Hospital, LMU Munich, 80337 Munich, Germany.

Philipp Harter (P)

Department of Gynecology and Gynecologic Oncology, Kliniken Essen-Mitte, 45136 Essen, Germany.

Olli Carpén (O)

Institute of Biomedicine and FICAN West Cancer Centre Cancer Research Unit, University of Turku, 20521 Turku, Finland.
Department of Pathology and Research Program in Systems Oncology, University of Helsinki and Helsinki University Hospital, 00014 Helsinki, Finland.

Kaisa Huhtinen (K)

Institute of Biomedicine and FICAN West Cancer Centre Cancer Research Unit, University of Turku, 20521 Turku, Finland.

Johanna Hynninen (J)

Department of Obstetrics and Gynecology, Turku University Hospital and University of Turku, 20521 Turku, Finland.

Mika Hilvo (M)

Zora Biosciences Oy, 02150 Espoo, Finland.

Classifications MeSH