Bibliometric Analysis of Chimeric Antigen Receptor-Based Immunotherapy in Cancers From 2001 to 2021

Zhanpeng Ou1, Ling Qiu1, Haixu Rong1

  • 1Guangdong Provincial Key Laboratory of Malignant Tumor Epigenetics and Gene Regulation, Sun Yat-sen Memorial Hospital, Guangzhou, China.

Abstract

Insights

Chimeric antigen receptor (CAR)-based immunotherapy shows promise for treating cancers. Research trends highlight overcoming challenges in solid tumors and developing safer CAR-engineered cell products for enhanced cancer treatment.

Area of Science:

  • Immunotherapy
  • Oncology
  • Biotechnology

Background:

  • Chimeric antigen receptor (CAR)-based immunotherapy demonstrates significant potential for treating both blood cancers and solid tumors.
  • Clinical development of CAR-based immunotherapy faces several persistent obstacles.
  • This study aims to map the research landscape and identify key trends in CAR-based immunotherapy.

Purpose of the Study:

  • To summarize the research landscape of CAR-based immunotherapy.
  • To highlight the front lines and emerging trends in the field.
  • To identify key research areas and influential contributors.

Main Methods:

  • Bibliometric analysis of literature published from 2001 to 2021 from the Web of Science Core Collection.
  • Data extraction and screening of full records and cited references.
  • Visualization and analysis using CiteSpace, Microsoft Excel 2019, VOSviewer, and R software.

Main Results:

  • A total of 5981 articles and reviews were analyzed, showing increasing publication and citation trends over 20 years.
  • The United States led in publications and collaborations, with China and Germany also being significant contributors.
  • Key research hotspots include multiple myeloma, safety and toxicity, solid tumors, CAR-engineered non-T cells, and gene editing.

Conclusions:

  • CAR-based immunotherapy is a promising cancer treatment modality.
  • Advanced gene modification technologies are crucial for overcoming therapeutic challenges, particularly in solid tumors.
  • The field is moving towards developing safer, more effective universal CAR-engineered cell products.

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