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Updated: Feb 7, 2026

An Orthotopic Model of Serous Ovarian Cancer in Immunocompetent Mice for in vivo Tumor Imaging and Monitoring of Tumor Immune Responses
Published on: November 28, 2010
Bibliometric analysis of ovarian cancer immune evasion research from 2015 to 2024
Xiaodong Wang1, Di Xiong2, Songli Cui1
1Department of Oncology, Zhuzhou Hospital Affiliated to Xiangya School of Medicine, Central South University, Zhuzhou, China.
Background:
Ovarian cancer remains lethal and shows limited response to immunotherapy partly due to immune evasion. We mapped global research trends on ovarian cancer immune evasion during 2015-2024.
Methods:
Web of Science Core Collection and Scopus were searched on 6 Oct 2025 for English articles and reviews published 1 Jan 2015-31 Dec 2024. Records were merged and deduplicated in R (bibliometrix). Productivity, collaboration, keywords, thematic clusters, and burst terms and citations were analyzed using bibliometrix, VOSviewer, and CiteSpace.
Results:
A total of 496 publications from 202 sources were included, showing rapid growth (annual growth rate ~24.6%) with a marked rise after 2020. The United States and China contributed the most output, whereas international collaboration was limited (~9.7% of authors with multiple-country affiliations). Keyword co-occurrence revealed major themes in immunotherapy, tumor microenvironment remodeling, immune checkpoint regulation, resistance mechanisms, and genetic/epigenetic modulation. Emerging hotspots highlighted tumor-associated macrophages and STAT3-centered signaling as key drivers of immune suppression and therapeutic resistance.
Conclusion:
Research on ovarian cancer immune evasion is expanding quickly and is shifting toward actionable targets and combination strategies. Strengthening cross-country collaboration and focusing on TME- and STAT3/TAM-directed interventions may accelerate translation and improve immunotherapy outcomes.
Insights
Ovarian cancer immune evasion research is rapidly growing, focusing on tumor microenvironment and STAT3/TAM targets. Enhanced collaboration and targeted interventions are key to improving immunotherapy outcomes.
Area of Science:
- Oncology
- Immunology
- Bibliometrics
Background:
- Ovarian cancer presents a significant challenge due to its lethality and poor response to immunotherapy, largely attributed to immune evasion mechanisms.
- Understanding global research trends in ovarian cancer immune evasion is crucial for advancing treatment strategies.
Purpose of the Study:
- To map and analyze global research trends in ovarian cancer immune evasion from 2015 to 2024.
- To identify key themes, emerging hotspots, and collaboration patterns in this research field.
Main Methods:
- Bibliometric analysis of publications from Web of Science and Scopus databases (2015-2024).
- Utilized bibliometrix, VOSviewer, and CiteSpace for analyzing productivity, collaboration, keywords, thematic clusters, and burst terms.
- Included English articles and reviews, with records merged and deduplicated.
Main Results:
- A total of 496 publications from 202 sources were identified, demonstrating a significant annual growth rate of ~24.6%, with accelerated growth post-2020.
- The United States and China were leading contributors, but international collaboration remained limited.
- Key research themes included immunotherapy, tumor microenvironment remodeling, immune checkpoint regulation, resistance mechanisms, and genetic/epigenetic modulation.
- Emerging research hotspots identified tumor-associated macrophages (TAMs) and STAT3-centered signaling as critical drivers of immune suppression and therapeutic resistance.
Conclusions:
- Research on ovarian cancer immune evasion is rapidly expanding, with a clear shift towards identifying actionable targets and combination therapies.
- Strengthening international research collaboration is essential.
- Focusing on interventions targeting the tumor microenvironment (TME) and STAT3/TAM pathways holds promise for accelerating translation and improving immunotherapy efficacy.
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