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过去 15 年三阴性乳腺癌过继性细胞治疗全球研究趋势的文献计量学分析

英文原题:A bibliometric analysis of global research trends in adoptive cell therapy for triple negative breast cancer over the past 15 years.

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A bibliometric analysis of global research trends in adoptive cell therapy for triple negative breast cancer over the past 15 years.

PubMed 2026/06/10(内容时间) Discov Oncol Q3 · IF 2.8(JCR 2025)

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研究概要

过去十年间,TNBC 中 ACT 的研究显著增长,反映出未被满足的临床需求以及日益增长的科学兴趣。

中文摘要

侵袭性且具有多样性的三阴性乳腺癌(TNBC)临床结局较差,特异性治疗选择有限。过继细胞治疗(ACT)已成为有前景的免疫治疗策略,包括TIL(肿瘤浸润淋巴细胞)、T细胞受体工程化T细胞及CAR-T(CAR-T)细胞。然而,其在TNBC中的临床应用仍面临困难。本研究采用文献计量学方法,全面评估TNBC ACT领域的新兴热点、知识结构及全球研究趋势。

检索Scopus数据库中2011至2025年发表的TNBC ACT相关文献,仅纳入英文原创研究和综述。使用VOSviewer(1.6.20版)和Microsoft Excel 2021分析文献计量指标,包括年度发文量、国家和机构贡献、作者合作、引用特征及关键词共现。通过网络可视化和聚类分析考察主题演变与合作模式。

共检索到8496篇文献,复合年增长率超过60%,研究产出呈指数级增长,尤其是2020年以后。中国和美国合计占所有文献的60%以上,在全球研究产出中占主导地位。核心研究网络集中于少数机构和高产作者。关键词分析显示,从基础和临床前研究中逐渐形成了若干面向临床的主题,包括CAR-T 细胞疗法、肿瘤微环境调控、免疫检查点抑制、代谢重编程及生物标志物驱动的方法。尽管研究活跃度提高,文献仍显示实体瘤转化应用面临肿瘤异质性、抗原不稳定、免疫抑制性微环境和安全性等持续挑战。

过去十年,TNBC ACT研究显著增长,反映了未满足的临床需求和科学界不断增强的兴趣。然而,科学领导力仍集中于少数机构,且研究理念正在转向联合方法和新一代工程策略,凸显持续克服生物学和转化限制的必要性。本计量分析全面呈现了该领域现状,可为未来研究、协作及开发更有效的TNBC ACT策略提供方向。

展开英文摘要原文

The aggressive and diverse subtype of breast cancer known as triple-negative breast cancer (TNBC) has poor clinical outcomes and few specific therapeutic choices. Tumor-infiltrating lymphocytes (TILs), T-cell receptor-engineered T cells, and chimeric antigen receptor T (CAR-T) cells are examples of adoptive cell therapy (ACT), which has become a promising immunotherapeutic approach. Its clinical application in TNBC is still difficult, nevertheless. This study used bibliometric techniques to thoroughly assess growing hotspots, intellectual structure, and worldwide research trends pertaining to ACT in TNBC.

The Scopus database was searched for publications related to ACT in TNBC from 2011 to 2025. There were only original articles and reviews written in English. VOSviewer (version 1.6.20) and Microsoft Excel 2021 were used to analyse bibliometric indicators, such as annual publication output, country and institutional contributions, authorship patterns, citation characteristics, and keyword co-occurrence. To investigate thematic evolution and collaboration patterns, network visualisation and clustering analysis were carried out.

With a compound annual growth rate of more than 60%, a total of 8,496 publications were found, indicating an exponential rise in research output, especially beyond 2020. Together, China and the US accounted for over 60% of all publications, dominating the world's research output. The core research network was made up of a few institutions and very productive writers. CAR-T cell therapy, tumor microenvironment manipulation, immunological checkpoint inhibition, metabolic reprogramming, and biomarker-driven methods were among the clinically orientated themes that emerged from foundational and preclinical investigations, according to keyword analysis. The literature shows ongoing translational difficulties with regard to tumor heterogeneity, antigen instability, immunosuppressive microenvironments, and safety concerns in solid tumors, despite increased research activity.

Over the past ten years, research on ACT in TNBC has grown significantly, reflecting both unmet clinical need and growing scientific interest. However, continuous efforts to overcome biological and translational constraints are highlighted by the concentration of scientific leadership and the conceptual move towards combination methods and next-generation engineering approaches. This bibliometric analysis offers a thorough picture of the state of the field and could direct future research, teamwork, and the creation of more potent ACT tactics for TNBC.

论文信息

作者
Elenien WIA、Ibrahim NA、Mohamed M、Elenien YA、Heiba M、Abouelenin O、Mahmood DA、Hussein FK
第一作者单位
Faculty of Pharmacy, Alexandria University, Alexandria, Egypt. Wesamaboelenien2003@gmail.com.Egypt
通讯作者单位
Department of Biology, College of Education for Pure Sciences, University of Kirkuk, Kirkuk, 36001, Iraq. farhankhaleel@uokirkuk.edu.iq.
期刊
Discover oncology2026 Jun 10
原文标识
PubMed 42268462 · DOI 10.1007/s12672-026-05277-6