A Bibliometric Analysis of Immunotherapy in Diffuse large B-cell lymphoma from 2004 to 2024

免疫疗法 淋巴瘤 癌症 医学 弥漫性大B细胞淋巴瘤 癌症免疫疗法 肿瘤科 疾病 内科学
作者
Yanling Wu,Xiaomin Chen,Yang Liu,Yu Zhao,Ling Luo,Qiuwen Mi,Xiaoying Wen,Chunlan Huang
出处
期刊:Acta Haematologica [Karger Publishers]
卷期号:: 1-31
标识
DOI:10.1159/000545152
摘要

Introduction: Immunotherapy in DLBCL (diffuse large B-cell lymphoma disease) has become an active research area with great value and potential. However, bibliometric research in this area is still sparse. Through bibliometric analysis, we aimed to visualize the research hot spots and trends of immunotherapy in DLBCL disease to help understand the future development of basic and clinical research. Methods: The Web of Science Core Collection database was searched for articles and reviews related to the immunotherapy of DLBCL from 2004 to 2024. VOSviewers, CiteSpace, and the R package “bibliometrix” were used to conduct the bibliometric analysis. Results: A total of 662 articles were included. The number of immunotherapy treatments in DLBCL increased year by year. The publications came from 55 countries, led by the United States and the People’s Republic of China, and 1,349 institutions, with the leading research institutions being The University of Texas MD Anderson Cancer Center and Memorial Sloan Kettering Cancer Center. Leukemia & lymphoma is the journal with the most research, and Blood is the journal with the most co-citations. We identified 4833 authors, among which Young and Ken H had the most significant articles, while Neelapu SS had the largest number of co-citations. After analysis, the most common keyword is CAR T. CAR T cells (chimeric antigen receptor T cells immunotherapy), a current and developing area of research. Conclusions: This is the first bibliometric study to comprehensively summarize research trends and advances in immunotherapy in DLBCL disease. This information will provide a reference for researchers and healthcare providers in immunotherapy research by clarifying recent research frontiers and hotspots such as CAR T cells, bispecific antibodies, and so on.

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