Organoids and epithelial ovarian cancer - a future tool for personalized treatment decisions? (Review)

Yagmur Sisman1,2, Tine Schnack3, Estrid Høgdall2

  • 1Department of Gynecology, Copenhagen University Hospital, Rigshospitalet, 2100 Copenhagen, Denmark.

Insights

Patient-derived organoids show promise for predicting epithelial ovarian cancer (EOC) treatment response. While they can model tumor heterogeneity, more research is needed to confirm their clinical utility in guiding chemotherapy and gene-targeting therapies.

Area of Science:

  • Oncology
  • Biotechnology
  • Genomics

Background:

  • Epithelial ovarian cancer (EOC) is a leading cause of cancer death in women.
  • Most EOC cases initially respond to treatment but often recur with chemoresistance.
  • Predictive biomarkers are crucial for personalized treatment strategies in EOC.

Purpose of the Study:

  • To systematically review the current applications of patient-derived organoids for drug screening in EOC.
  • To assess the potential of organoids in predicting treatment response for EOC patients.

Main Methods:

  • A systematic literature search was conducted using PubMed and the Cochrane Library.
  • Studies investigating ovarian cancer and organoids were included based on specific criteria.
  • Data on organoid growth rates, clinical outcomes, and heterogeneity were extracted.

Main Results:

  • Ten studies met the inclusion criteria, with organoid growth rates ranging from 29% to 90%.
  • Four studies reported a positive correlation between organoid drug screening results and clinical response.
  • Seven studies confirmed that organoids effectively recapitulate inter- and intratumoral heterogeneity.

Conclusions:

  • Patient-derived organoids show potential as a platform for predicting chemotherapy and gene-targeting therapy response in EOC.
  • Current evidence is exploratory, with a limited number of published drug screening studies.
  • Further research is essential to validate organoids for guiding oncological treatment decisions in EOC.

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