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卵巢癌PARP抑制剂的全球研究趋势:一项文献计量分析

Global research trends in PARP inhibitors for ovarian cancer: a bibliometric analysis.

作者信息

Wang Xiaodong, Ding Gouping, He Jing, Huang Yiping, Wang Qianqian

机构信息

Department of Oncology, The Second Xiangya Hospital, Central South University, Changsha, 410011, Hunan, China.

Department of Oncology, Zhuzhou Hospital Affiliated to Xiangya School of Medicine, Central South University, Zhuzhou, China.

出版信息

Discov Oncol. 2025 Aug 25;16(1):1614. doi: 10.1007/s12672-025-03487-y.


DOI:10.1007/s12672-025-03487-y
PMID:40853616
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12379664/
Abstract

This bibliometric analysis maps global research trends on PARP inhibitors (PARPis) in ovarian cancer from January 2021 to May 2025, utilizing 1,434 publications retrieved from the Web of Science Core Collection. Employing Bibliometrix, VOSviewer, and CiteSpace, the study quantifies contributions across countries, institutions, authors, and research foci. Key findings reveal the United States (440 publications) and China (352) as leading producers, with UNICANCER (287 publications) and Memorial Sloan Kettering Cancer Center (61) as top institutions. Keyword clustering identified six research themes: PARPi resistance mechanisms (Cluster 1, red) emerged as the dominant focus, followed by immunotherapy combinations for platinum-resistant disease (Cluster 2, green), maintenance therapy (Cluster 3, blue), BRCA mutations (Cluster 4, yellow), applications beyond ovarian cancer (Cluster 5, purple), and anti-angiogenic mechanisms (Cluster 6, light blue). Temporal analysis highlighted an evolution from foundational research (e.g., DNA repair pathways) toward clinical translation (e.g., maintenance therapy optimization). Notable citation bursts surrounded clinical milestones, including the SOLO1 trial's 7-year overall survival data (burst strength: 23.99), underscoring the field's emphasis on survival outcomes. Critical gaps persist in understanding resistance mechanisms and developing immuno-combination strategies, which constituted only 4.8% of keyword frequency. The study underscores the need for intensified research into resistance mitigation and transnational collaboration, particularly between established Euro-American networks and emerging East Asian hubs, to address therapeutic challenges and optimize clinical impact.

摘要

这项文献计量分析描绘了2021年1月至2025年5月全球卵巢癌中PARP抑制剂(PARPis)的研究趋势,使用了从科学网核心合集检索到的1434篇出版物。该研究利用文献计量学、VOSviewer和CiteSpace量化了各国、机构、作者和研究重点的贡献。主要发现显示,美国(440篇出版物)和中国(352篇)是主要产出国,UNICANCER(287篇出版物)和纪念斯隆凯特琳癌症中心(61篇)是顶尖机构。关键词聚类确定了六个研究主题:PARPi耐药机制(第1组,红色)成为主要焦点,其次是铂耐药疾病的免疫治疗联合(第2组,绿色)、维持治疗(第3组,蓝色)、BRCA突变(第4组,黄色)、卵巢癌以外的应用(第5组,紫色)和抗血管生成机制(第6组,浅蓝色)。时间分析突出了从基础研究(如DNA修复途径)向临床转化(如维持治疗优化)的演变。显著的引用爆发围绕着临床里程碑,包括SOLO1试验的7年总生存数据(爆发强度:23.99),强调了该领域对生存结果的重视。在理解耐药机制和开发免疫联合策略方面仍然存在关键差距,这些仅占关键词频率的4.8%。该研究强调需要加强对耐药缓解的研究和跨国合作,特别是在成熟的欧美网络和新兴的东亚中心之间,以应对治疗挑战并优化临床影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c932/12379664/53e1b3c8defe/12672_2025_3487_Fige_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c932/12379664/b1c4c45a753d/12672_2025_3487_Figa_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c932/12379664/c8153bf0c2bc/12672_2025_3487_Figb_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c932/12379664/f4c8e291113b/12672_2025_3487_Figc_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c932/12379664/481cb7868327/12672_2025_3487_Figd_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c932/12379664/53e1b3c8defe/12672_2025_3487_Fige_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c932/12379664/b1c4c45a753d/12672_2025_3487_Figa_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c932/12379664/c8153bf0c2bc/12672_2025_3487_Figb_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c932/12379664/f4c8e291113b/12672_2025_3487_Figc_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c932/12379664/481cb7868327/12672_2025_3487_Figd_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c932/12379664/53e1b3c8defe/12672_2025_3487_Fige_HTML.jpg

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Global research trends in PARP inhibitors for ovarian cancer: a bibliometric analysis.

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本文引用的文献

[1]
Homologous recombination deficiency (HRD) testing landscape: clinical applications and technical validation for routine diagnostics.

Biomark Res. 2025-2-21

[2]
Functional evaluation and clinical classification of BRCA2 variants.

Nature. 2025-2

[3]
Saturation genome editing-based clinical classification of BRCA2 variants.

Nature. 2025-2

[4]
PARP inhibitors in ovarian cancer.

Semin Oncol. 2024

[5]
BRCA2 promotes genomic integrity and therapy resistance primarily through its role in homology-directed repair.

Mol Cell. 2024-2-1

[6]
Safety of PARP inhibitors as maintenance therapy in ovarian cancer.

Expert Opin Drug Saf. 2023

[7]
PARP Inhibitors in Newly Diagnosed and Recurrent Ovarian Cancer.

Am J Clin Oncol. 2023-9-1

[8]
PARP Inhibitors in Ovarian Cancer: A Review.

Target Oncol. 2023-7

[9]
Targeting DNA damage response pathways in cancer.

Nat Rev Cancer. 2023-2

[10]
Overall Survival With Maintenance Olaparib at a 7-Year Follow-Up in Patients With Newly Diagnosed Advanced Ovarian Cancer and a BRCA Mutation: The SOLO1/GOG 3004 Trial.

J Clin Oncol. 2023-1-20

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