[Current advances in immunotherapy in ovarian cancer]
Related Experiment Video
Updated: Dec 27, 2025

Author Spotlight: Advancing Personalized Medicine in Ovarian Cancer
Published on: February 23, 2024
Olivia Le Saux1, Bertrand Dubois2, Marc-Henri Stern3
1Hospices civils de Lyon, service d'oncologie médicale, 165, chemin du grand Revoyet, 69495 Pierre-Bénite, France; Université Claude-Bernard Lyon I, centre de recherche en cancérologie de Lyon, CNRS 5286, centre Léon-Bérard, Inserm 1052, 69008 Lyon, France.
Abstract:
Ovarian cancers express highly immunogenic tissue-specific antigens. The resulting immune infiltration is a major prognostic factor. There is therefore a strong biological rationale for the development of immunotherapy in ovarian cancer. However, based on Phase I and II clinical trials data, the efficacy of anti-PD-1 and anti-PD-L1 immune checkpoint inhibitors (ICPIs) remains limited in monotherapy in heavily pre-treated patients. Currently, the identification of predictive biomarkers of response and resistance is one of the major areas of research. Identifying effective combination of anti-PD-1 or anti-PD-L1 with other anticancer agents is another clinical need. Several combinations were evaluated. The association of ICPIs with chemotherapy (anthracyclines or carboplatin+paclitaxel) is disappointing (JAVELIN studies). The association with PARP inhibitors, anti-angiogenic agents and CTLA-4 inhibitors seems promising. Other immune therapies such as cell therapies (adoptive transfer of intra-tumor lymphocytes, CAR T cells or vaccines from dendritic cells) could be the future of immunotherapy in ovarian cancer but only early phase studies clinical data is available at this time.
Insights
Immunotherapy shows promise for ovarian cancer, but anti-PD-1/PD-L1 drugs alone have limited efficacy. Combinations with other agents and cell therapies are areas of active research for improved treatment outcomes.
Area of Science:
- Oncology
- Immunology
- Cancer Therapy
Background:
- Ovarian cancers possess immunogenic antigens, leading to immune infiltration that impacts prognosis.
- Immunotherapy is a biologically rational approach for ovarian cancer treatment.
- Current anti-PD-1/PD-L1 immune checkpoint inhibitors (ICPIs) show limited efficacy as monotherapy in heavily pre-treated ovarian cancer patients.
Purpose of the Study:
- To review the current landscape of immunotherapy in ovarian cancer.
- To identify predictive biomarkers for response and resistance to ICPIs.
- To explore effective combination strategies for anti-PD-1 or anti-PD-L1 therapy.
Main Methods:
- Review of Phase I and II clinical trial data for ICPIs in ovarian cancer.
- Evaluation of various combination therapies with ICPIs.
- Assessment of emerging immunotherapeutic approaches, including cell therapies.
Main Results:
- Monotherapy with anti-PD-1/PD-L1 agents has shown limited success in heavily pre-treated patients.
- Combinations of ICPIs with chemotherapy have yielded disappointing results.
- Promising results are emerging from combinations of ICPIs with PARP inhibitors, anti-angiogenic agents, and CTLA-4 inhibitors.
Conclusions:
- Identifying predictive biomarkers is crucial for optimizing ICPI efficacy in ovarian cancer.
- Combination therapies, particularly with PARP inhibitors, anti-angiogenic agents, and CTLA-4 inhibitors, hold significant promise.
- Cell-based immunotherapies represent a potential future direction, though further clinical data is needed.
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10:35An Orthotopic Model of Serous Ovarian Cancer in Immunocompetent Mice for in vivo Tumor Imaging and Monitoring of Tumor Immune Responses
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07:59Evaluating the Angiogenetic Properties of Ovarian Cancer Stem-Like Cells using the Three-Dimensional Co-Culture System, NICO-1
Published on: December 5, 2020
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