J Gynecol Oncol.  2021 Mar;32(2):e18. 10.3802/jgo.2021.32.e18.

Ovarian cancer risk score predicts chemo-response and outcome in epithelial ovarian carcinoma patients

Affiliations
  • 1Graduate Institute of Molecular Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan
  • 2Department of Obstetrics and Gynecology, College of Medicine, National Taiwan University, Taipei, Taiwan
  • 3Department of Obstetrics and Gynecology, National Taiwan University Hospital, Hsin-Chu Branch, HsinChu City, Taiwan
  • 4Department of Obstetrics and Gynecology, National Taiwan University Hospital, Yun-Lin Branch, Douliou, Taiwan
  • 5Graduate Institute of Clinical Medicine, College of Medicine, National Taiwan University, Taipei, Taiwan
  • 6Graduate Institute of Oncology, College of Medicine, National Taiwan University, Taipei, Taiwan

Abstract


Objective
Cytoreductive surgery followed by adjuvant chemotherapy is a standard frontline treatment for epithelial ovarian cancer (EOC). We aimed to develop an ovarian cancer risk score (OVRS) based on the expression of 10 ovarian-cancer-related genes to predict the chemoresistance, and outcomes of EOC patients.
Methods
We designed a case-control study with total 149 EOC women including 75 chemosensitives and 74 chemoresistants. Gene expression was measured using the quantitative real-time polymerase chain reaction. We tested for correlation between the OVRS and chemosensitivity or chemoresistance, disease-free survival (DFS), and overall survival (OS), and validated the OVRS by analyzing patients from the TCGA database.
Results
The chemosensitive group had lower OVRS than the chemoresistant group (5 vs. 15, p≤0.001, Mann-Whitney U test). Patients with disease relapse (13 vs. 5, p<0.001, MannWhitney U test) or disease-related death (13.5 vs. 6, p<0.001) had higher OVRS than those without. OVRS ≥10 (hazard ratio=3.29; 95% confidence interval=1.94–5.58; p<0.001) was the only predictor for chemoresistance in multivariate analysis. The median DFS (5 months vs. 24 months) and OS (39 months vs. >60 months) of patients with OVRS ≥10 were significantly shorter than those of patients with OVRS <9). The high OVRS group also had significantly shorter median OS than the low OVRS group in 255 patients in the TCGA database (39 vs. 49 months, p=0.046).
Conclusions
Specific genes panel can be clinically applied in predicting the chemoresistance and outcome, and decision-making of epithelial ovarian cancer.

Keyword

Ovarian Cancer; Prognostic Factor; Gene Analysis; Drug Resistance; Risk Score
Full Text Links
  • JGO
Actions
Cited
CITED
export Copy
Close
Share
  • Twitter
  • Facebook
Similar articles
Copyright © 2024 by Korean Association of Medical Journal Editors. All rights reserved.     E-mail: koreamed@kamje.or.kr