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程序性死亡受体1/程序性死亡配体1抑制剂相关不良事件:2014年至2024年的文献计量分析

PD-1/PD-L1 inhibitors related adverse events: A bibliometric analysis from 2014 to 2024.

作者信息

Song Qingya, Yu Zongliang, Lu Wenping, Zhuo Zhili, Chang Lei, Mei Heting, Cui Yongjia, Zhang Dongni

机构信息

Department of Oncology, Guang'anmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.

Graduate School, Beijing University of Chinese Medicine, Beijing, China.

出版信息

Hum Vaccin Immunother. 2025 Dec;21(1):2424611. doi: 10.1080/21645515.2024.2424611. Epub 2025 Jan 6.

Abstract

Programmed cell death-1 (PD-1) inhibitors and programmed cell death ligand 1 (PD-L1) inhibitors are considered effective alternatives for the primary treatment of recurrent metastatic cancers. However, they can induce various adverse events affecting multiple organ systems, potentially diminishing patients' quality of life, and even leading to treatment interruptions. Adverse events related to PD-1/PD-L1 inhibitors differ from those associated with CTLA-4 inhibitors and are more commonly observed in the treatment of solid tumors. This study aimed to address the knowledge gap regarding adverse events related to PD-1/PD-L1 inhibitors. A visual bibliometric network was constructed using VOSviewer, CiteSpace, R software, and the Web of Science Core Collection (WoSCC) to quantitatively analyze this research field. Future research directions were also explored. The USA ranked first in publication count and total citations. Over time, publication types transitioned from case reports to clinical trials. Research on for nivolumab was the most prevalent. The spectrum of cancers treated by PD-1/PD-L1 inhibitors expanded beyond melanoma and lung cancer to include renal cell carcinoma, esophageal cancer, and others. Common adverse events included pneumonitis, myasthenia gravis, and vitiligo. There was a significant increase in multi-phase clinical trials and studies related to biomarkers. This study offers valuable insights for potential collaborators and institutions, highlighting trends in the study of adverse events related to PD-1/PD-L1 inhibitors. The management of these adverse events has become more refined and standardized. Biomarker research and multi-phase clinical trials are likely to be key areas of focus in future studies.

摘要

程序性细胞死亡蛋白1(PD-1)抑制剂和程序性细胞死亡配体1(PD-L1)抑制剂被认为是复发性转移性癌症一线治疗的有效替代方案。然而,它们可诱发影响多个器官系统的各种不良事件,可能降低患者的生活质量,甚至导致治疗中断。与PD-1/PD-L1抑制剂相关的不良事件不同于与细胞毒性T淋巴细胞相关抗原4(CTLA-4)抑制剂相关的不良事件,且在实体瘤治疗中更常见。本研究旨在填补与PD-1/PD-L1抑制剂相关不良事件的知识空白。使用VOSviewer、CiteSpace、R软件和科学网核心合集(WoSCC)构建可视化文献计量网络,以定量分析该研究领域。还探索了未来的研究方向。美国在发表数量和总被引次数方面排名第一。随着时间的推移,发表类型从病例报告转变为临床试验。对纳武单抗的研究最为普遍。PD-1/PD-L1抑制剂治疗的癌症谱已从黑色素瘤和肺癌扩展到包括肾细胞癌、食管癌等。常见的不良事件包括肺炎、重症肌无力和白癜风。多阶段临床试验和与生物标志物相关的研究显著增加。本研究为潜在的合作者和机构提供了有价值的见解,突出了与PD-1/PD-L1抑制剂相关不良事件研究的趋势。这些不良事件的管理已变得更加精细和规范。生物标志物研究和多阶段临床试验可能是未来研究的关键重点领域。

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