Abstract
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 lip-idome 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 unad-justed 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.
| Original language | English |
|---|---|
| Article number | 1764 |
| Journal | Cancers |
| Volume | 13 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - 2 Apr 2021 |
| MoE publication type | A1 Journal article-refereed |
Funding
Funding: L.S. and J.H. were financially supported by the Clinical Research (VTR) Fund of the Turku University Hospital, K.H. by the Cancer Society of South‐West Finland, and O.C. by Finnish Cancer Society, Sigrid Juselius Foundation, and Finska Läkaresälskapet.
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 3 Good Health and Well-being
Keywords
- Bi-omarker
- Ceramide
- Lipid
- Lipidomics
- Outcome
- Ovarian cancer
- Patient stratification
- Personalized medicine
- Phospholipid
- Plasmalogen
- Prognosis
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