Affiliations 

  • 1 Department of Immunology & Pathology, Monash University, Central Clinical School, Level 6, 89, Commercial Road, Melbourne, 3181, VIC, Australia
  • 2 Biostatistics Consulting Platform, Central Clinical School, Monash University, Central Clinical School, Level 6, Commercial Road, Melbourne, 3181, VIC, Australia
  • 3 Gynae-oncology Unit, Royal Women's Hospital, 20 Flemington Road, Parkville, Melbourne, Victoria, 3052, Australia
  • 4 Epworth Research Institute, Epworth Healthcare, Richmond, 3121, Australia
  • 5 Centre for Cancer Research, Hudson Institute of Medical Research, 27-31 Wright St, Clayton, VIC, 3168, Australia
  • 6 Department of Immunology & Pathology, Monash University, Central Clinical School, Level 6, 89, Commercial Road, Melbourne, 3181, VIC, Australia. magdalena.plebanski@rmit.edu.au
Sci Rep, 2020 02 10;10(1):2213.
PMID: 32042020 DOI: 10.1038/s41598-020-59009-z

Abstract

Pre-operative discrimination of malignant masses is crucial for accurate diagnosis and prompt referral to a gynae oncology centre for optimal surgical intervention. HGSOC progression is correlated with local and systemic inflammation. We hypothesised that inclusion of inflammatory biomarkers in sera may improve diagnostic tests. In the training cohort, we tested four existing clinical tests (RMI score and ROMA, CA125 and HE4) and a panel of 28 immune soluble biomarkers in sera from 66 patients undergoing surgery for suspected ovarian cancer. Six promising immune biomarkers alone, or in combination with conventional tests, were subsequently analysed in an independent validation cohort (n = 69). IL-6 was identified as the main driver of variability followed closely by conventional diagnostic tests. Median sera IL-6 was higher in HGSOC patients compared to those with a benign mass or controls with normal ovaries (28.3 vs 7.3 vs 1.2 pg/ml, p  3.75 pg/ml as primary triage followed by conventional tests (CA125 or RMI score) identified ovarian cancer in patients with a misclassification rate of 4.54-3.03%, superior to the use of CA125 or RMI alone (9.09 to 10.60). The validation cohort demonstrated a similar improvement in the diagnostic sensitivity following addition of IL-6. IL-6 in combination with conventional tests may be a useful clinical biomarker for triage of patients with a suspected malignant ovarian mass.

* Title and MeSH Headings from MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.

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