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肝细胞癌中PD-1/PD-L1免疫治疗的结构与时间动态分析:历史、研究热点及新趋势

Structural and temporal dynamics analysis of PD-1/PD-L1 immunotherapy in hepatocellular carcinoma: History, research hotspots, and emerging trends.

作者信息

Tuergan Talaiti, Abulaiti Aimitaji, Shao Yingmei, Aji Tuerganaili

机构信息

Hepatobiliary and Echinococcosis Surgery Department, Digestive and Vascular Surgery Center, First Affiliated Hospital of Xinjiang Medical University, Urumqi, China.

出版信息

Hum Vaccin Immunother. 2025 Dec;21(1):2540143. doi: 10.1080/21645515.2025.2540143. Epub 2025 Aug 17.


DOI:10.1080/21645515.2025.2540143
PMID:40820303
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12363510/
Abstract

This research aims to explore the historical evolution, key research areas, and new trends in PD-1/PD-L1 immunotherapy for hepatocellular carcinoma (HCC) over the last twenty years, focusing on structural and temporal dynamics. The Web of Science Core Collection (WoSCC) database was used to gather studies on PD-1/PD-L1 immunotherapy for HCC.CiteSpace and HistCite were utilized for a bibliometric analysis to investigate the historical progression, research evolution, and emerging trends in this area. In the last two decades, 2804 papers on PD-1/PD-L1 immunotherapy in HCC have been published, comprising 541 reviews and contributions from 13,796 authors across 2,659 institutions. Since 2014, the number of annual publications has significantly increased, with extensive international collaboration. Several active research topics have emerged, covering 72 disciplines, generating 561 keywords, and 1,199 articles that experienced citation bursts. Cluster analysis of keywords revealed five emerging subfields: lenvatinib, immune escape, immne checkpoint inhibitors, prognostic models, and tumor microenvironment. According to the "Timeline visualization of references," classic topics include CMTM6, regulatory T cells, liver transplantation, and bioinformatics analysis, while emerging topics include prognosis, lenvatinib, transarterial chemoembolization, hepatic arterial infusion chemotherapy, and single-cell RNA sequencing. This study sheds light on the current status and developing trends in PD-1/PD-L1 immunotherapy research for HCC, offering researchers valuable insights to identify crucial areas and explore new research directions.

摘要

本研究旨在探讨过去二十年来肝细胞癌(HCC)的PD-1/PD-L1免疫疗法的历史演变、关键研究领域和新趋势,重点关注结构和时间动态。使用科学网核心合集(WoSCC)数据库收集关于HCC的PD-1/PD-L1免疫疗法的研究。利用CiteSpace和HistCite进行文献计量分析,以研究该领域的历史进展、研究演变和新趋势。在过去二十年中,已发表了2804篇关于HCC的PD-1/PD-L1免疫疗法的论文,其中包括541篇综述以及来自2659个机构的13796位作者的贡献。自2014年以来,年度出版物数量显著增加,且有广泛的国际合作。出现了几个活跃的研究主题,涵盖72个学科,产生了561个关键词以及1199篇经历了引用爆发的文章。关键词聚类分析揭示了五个新兴子领域:乐伐替尼、免疫逃逸、免疫检查点抑制剂、预后模型和肿瘤微环境。根据“参考文献的时间线可视化”,经典主题包括CMTM6、调节性T细胞、肝移植和生物信息学分析,而新兴主题包括预后、乐伐替尼、经动脉化疗栓塞、肝动脉灌注化疗和单细胞RNA测序。本研究揭示了HCC的PD-1/PD-L1免疫疗法研究的现状和发展趋势,为研究人员提供了宝贵的见解,以确定关键领域并探索新的研究方向。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e535/12363510/a98eb83a96f0/KHVI_A_2540143_F0009_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e535/12363510/55ba76b9e2b6/KHVI_A_2540143_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e535/12363510/66346c9c0cfe/KHVI_A_2540143_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e535/12363510/594763c66a5c/KHVI_A_2540143_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e535/12363510/dc451dc4431b/KHVI_A_2540143_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e535/12363510/947f6f1dbba9/KHVI_A_2540143_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e535/12363510/7b361e24e677/KHVI_A_2540143_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e535/12363510/e4015fdbfb83/KHVI_A_2540143_F0007_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e535/12363510/4be7728f392b/KHVI_A_2540143_F0008_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e535/12363510/a98eb83a96f0/KHVI_A_2540143_F0009_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e535/12363510/55ba76b9e2b6/KHVI_A_2540143_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e535/12363510/66346c9c0cfe/KHVI_A_2540143_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e535/12363510/594763c66a5c/KHVI_A_2540143_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e535/12363510/dc451dc4431b/KHVI_A_2540143_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e535/12363510/947f6f1dbba9/KHVI_A_2540143_F0005_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e535/12363510/7b361e24e677/KHVI_A_2540143_F0006_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e535/12363510/e4015fdbfb83/KHVI_A_2540143_F0007_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e535/12363510/4be7728f392b/KHVI_A_2540143_F0008_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e535/12363510/a98eb83a96f0/KHVI_A_2540143_F0009_OC.jpg

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本文引用的文献

[1]
Prognostic significance of the cachexia index (CXI) in patients with cancer: A systematic review and meta-analysis.

Clin Nutr ESPEN. 2025-3-27

[2]
The immunosuppressive role of MDSCs in HCC: mechanisms and therapeutic opportunities.

Cell Commun Signal. 2025-3-27

[3]
Sophisticated roles of tumor microenvironment in resistance to immune checkpoint blockade therapy in hepatocellular carcinoma.

Cancer Drug Resist. 2025-2-26

[4]
High serum levels of soluble PD‑1 and PD‑L1 are associated with advanced clinical stages in patients with cervical cancer.

Biomed Rep. 2025-2-19

[5]
E-twenty-six-specific sequence variant 5 (ETV5) facilitates hepatocellular carcinoma progression and metastasis through enhancing polymorphonuclear myeloid-derived suppressor cell (PMN-MDSC)-mediated immunosuppression.

Gut. 2025-6-6

[6]
Comprehensive analysis of publications concerning combinations of immunotherapy and targeted therapies for hepatocellular carcinoma: a bibliometric study.

Front Immunol. 2025-2-12

[7]
Identification of immunogenic HLA-A*02:01 epitopes associated with HCC for immunotherapy development.

Hepatol Commun. 2025-2-26

[8]
Complete Response to Immunotherapy in Patients With Hepatocellular Carcinoma.

JAMA Netw Open. 2025-2-3

[9]
Predicting hepatocellular carcinoma survival with artificial intelligence.

Sci Rep. 2025-2-20

[10]
Demographic and survival characteristics of untreated hepatocellular carcinoma patients: insights into the natural history and prognostic determinants.

Rev Esp Enferm Dig. 2025-7

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