# Knowledge mapping of immunotherapy in castration-resistant prostate cancer: a bibliometric and visualized study (2003–2022)

**Authors:** Xianfu Cai, Chenguang Ding, Yang Li, Jin Zheng, Wujun Xue

PMC · DOI: 10.3389/fruro.2023.1239328 · Frontiers in Urology · 2023-10-12

## TL;DR

This study maps the development of immunotherapy research for prostate cancer from 2003 to 2022 using bibliometric analysis and visualization.

## Contribution

The paper provides a visualized knowledge map and identifies emerging trends in immunotherapy for castration-resistant prostate cancer.

## Key findings

- The USA and China's National Cancer Center are leading in immunotherapy research for castration-resistant prostate cancer.
- Key research trends include membrane antigen expression, CTLA4 blockade, radium-223, and vaccines.
- Combining therapies to enhance immune response is expected to be a major future trend in the field.

## Abstract

To utilize bibliometric analysis to examine the literature about immunotherapy for castration-resistant prostate cancer published within the past two decades. Through this method, we aim to visualize and analyze the research progress in this field and identify the most recent trends and developments.

This research conducted a comprehensive literature review on immunotherapy for castration-resistant prostate cancer. The time frame spanned from January 2003 to December 2022, and the data were extracted from the Web of Science Core Collection database. The application of various software tools, such as CiteSpace, Bibliometrix, and VOSviewer, facilitated the visualization and analysis of the gathered data. These technological utilities illustrated the progression of prominent focus areas within the field.

After excluding irrelevant studies, 373 papers were selected for this study. The findings suggested that the field of immunotherapy for castration-resistant prostate cancer was rapidly developing. The USA was considered to have a significant early entrant advantage in this area and profoundly influenced the field. Similarly, China’s National Cancer center demonstrated notable advantages as a recent participant in this research domain. Major research institutions contributing to the field include the University of California, San Francisco; the University of Washington; and the Memorial Sloan Kettering Cancer Research Center. Notably, US authors James L. Gulley, Charles G. Drake, and Lawrence Fong had the largest number of publications in this area. The main research trends for immunotherapy of castration-resistant prostate cancer are membrane antigen expression, checkpoints T-lymphocyte-associated protein 4 (CTLA4) blockade, radium-223, and vaccines, and the refinement of establishing organoid models might fuel castration-resistant prostate cancer immunotherapy research in the ongoing development.

The key trends in immunotherapy research for castration-resistant prostate cancer are membrane antigen expression, CTLA4 blockade, radium-223, and vaccines. Exploring new immune pathways and combining different therapeutic approaches to enhance immune response will be a major trend in the field in the future.

## Linked entities

- **Proteins:** CTLA4 (cytotoxic T-lymphocyte associated protein 4)
- **Chemicals:** radium-223 (PubChem CID 6335825)
- **Diseases:** prostate cancer (MONDO:0005159)

## Full-text entities

- **Genes:** CTLA4 (cytotoxic T-lymphocyte associated protein 4) [NCBI Gene 1493] {aka ALPS5, CD, CD152, CELIAC3, CTLA-4, GRD4}
- **Diseases:** Cancer (MESH:D009369), prostate cancer (MESH:D011471), castration-resistant (MESH:D064129)
- **Chemicals:** radium-223 (MESH:C000615150)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

_Full body text omitted from this summary view._ Fetch the complete paper as Markdown: https://tomesphere.com/paper/PMC12327239/full.md

## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12327239/full.md

## References

37 references — full list in the complete paper: https://tomesphere.com/paper/PMC12327239/full.md

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Source: https://tomesphere.com/paper/PMC12327239