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Bibliometric analysis of targeted immunotherapy for osteosarcoma-current knowledge, hotspots and future perspectives.

作者信息

Hu Yunxiang, Yang Rui, Ni Shuai, Song Zefeng

机构信息

Department of Orthopaedic Trauma, The Second Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China.

School of Graduates, Dalian Medical University, Dalian, Liaoning, China.

出版信息

Front Immunol. 2025 Feb 10;15:1485053. doi: 10.3389/fimmu.2024.1485053. eCollection 2024.


DOI:10.3389/fimmu.2024.1485053
PMID:39995821
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11847827/
Abstract

OBJECTIVE: The objective of this study is to conduct a bibliometric analysis on examining the current condition, areas of interest, and rising trends of immunotherapy for osteosarcoma (ITFOS), as well as its importance in associated research domains. METHODS: An extensive collection of academic papers on the use of ITFOS was obtained from the Web of Science between January 1, 2000 and October 20, 2023. Then, using a variety of tools like HisCite, VOSviewer, CiteSpace, and the bibliometrix package, a bibliometric study was carried out. This study included the collection of information on country, institution, author, journal, and keywords. RESULTS: A comprehensive analysis was undertaken on a total of 616 publications obtained from 247 journals, encompassing the contributions of 3725 authors affiliated with 831 institutes spanning across 43 countries/regions. Notably, China exhibited the highest quantity of published 277 (44.99%) articles on ITFOS. The most productive institution was Zhejiang University, with 26 (4.22%) publications. The author with the highest publication output was Tsukahara, Tomohide from Japan with 15 (2.44%) publications. The article with the most citation was "DOI: 10.1200/JCO.2014.58.0225". Frontiers in Immunology demonstrated the highest level of productivity, having published a total of 31 (5.03%) articles. The most frequently used were "osteosarcoma," "immunotherapy," and "cancer,". Meanwhile, "sequencing", "prognostic signature" and "immune microenvironment" have been identified as the research frontiers for the forthcoming years. CONCLUSION: This paper provides a thorough evaluation of current research trends and advancements in ITFOS. It includes relevant research findings and emphasizes collaborative efforts among authors, institutions, and countries.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9172/11847827/549203519d21/fimmu-15-1485053-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9172/11847827/8c3926cd00f6/fimmu-15-1485053-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9172/11847827/4a2dfe363e8c/fimmu-15-1485053-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9172/11847827/ed9a2fe9c23d/fimmu-15-1485053-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9172/11847827/3fc541c76313/fimmu-15-1485053-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9172/11847827/be7dd0769c2f/fimmu-15-1485053-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9172/11847827/06fa69b01e18/fimmu-15-1485053-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9172/11847827/77b28d30ea35/fimmu-15-1485053-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9172/11847827/549203519d21/fimmu-15-1485053-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9172/11847827/8c3926cd00f6/fimmu-15-1485053-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9172/11847827/4a2dfe363e8c/fimmu-15-1485053-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9172/11847827/ed9a2fe9c23d/fimmu-15-1485053-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9172/11847827/3fc541c76313/fimmu-15-1485053-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9172/11847827/be7dd0769c2f/fimmu-15-1485053-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9172/11847827/06fa69b01e18/fimmu-15-1485053-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9172/11847827/77b28d30ea35/fimmu-15-1485053-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9172/11847827/549203519d21/fimmu-15-1485053-g008.jpg

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本文引用的文献

[1]
Camrelizumab in combination with doxorubicin, cisplatin, ifosfamide, and methotrexate in neoadjuvant treatment of resectable osteosarcoma: A prospective, single-arm, exploratory phase II trial.

Cancer Med. 2024-9

[2]
Stratifying osteosarcoma patients using an epigenetic modification-related prognostic signature: implications for immunotherapy and chemotherapy selection.

Transl Cancer Res. 2024-7-31

[3]
Long term survival in adult osteosarcoma patients treated with a two-drug regimen: Final results of the OSAD93 phase II study of the FSG-GETO.

Eur J Cancer. 2024-9

[4]
Exploring the impact of PDGFD in osteosarcoma metastasis through single-cell sequencing analysis.

Cell Oncol (Dordr). 2024-10

[5]
Construction of an ER stress-related prognostic signature for predicting prognosis and screening the effective anti-tumor drug in osteosarcoma.

J Transl Med. 2024-1-16

[6]
Exploring the relationship between metabolism and immune microenvironment in osteosarcoma based on metabolic pathways.

J Biomed Sci. 2024-1-12

[7]
Synergistic Chemoimmunotherapy Augmentation via Sequential Nanocomposite Hydrogel-Mediated Reprogramming of Cancer-Associated Fibroblasts in Osteosarcoma.

Adv Mater. 2024-4

[8]
A pilot study of multi-antigen stimulated cell therapy-I plus camrelizumab and apatinib in patients with advanced bone and soft-tissue sarcomas.

BMC Med. 2023-11-29

[9]
Single-cell and bulk RNA sequencing reveals Anoikis related genes to guide prognosis and immunotherapy in osteosarcoma.

Sci Rep. 2023-11-18

[10]
Exploratory study of an anti-PD-L1/TGF-β antibody, TQB2858, in patients with refractory or recurrent osteosarcoma and alveolar soft part sarcoma: a report from Chinese sarcoma study group (TQB2858-Ib-02).

BMC Cancer. 2023-9-15

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