Advancements in CAR-T Therapy: A Comprehensive Review

被引:0
作者
Tanwar, Aastha [1 ]
Targhotra, Monika [1 ]
Chauhan, Meenakshi Kanwar [1 ]
机构
[1] DPSR Univ, Delhi Inst Pharmaceut Sci & Res, Dept Pharmaceut, NDDS Res Lab, Pushp Vihar Sec 3,MB Rd, New Delhi 110017, India
关键词
CAR-T therapy; immunotherapy; pipeline molecules; cancer treatment; CHIMERIC ANTIGEN RECEPTORS; SPACER DOMAIN; CELL THERAPY; CANCER; TUMORS; IMMUNOTHERAPY; EFFICACY; REGIONS; DESIGN;
D O I
10.2174/0115733947320632240517093549
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chimeric Antigen Receptor T-cell (CAR-T) therapy has emerged as a ground-breaking approach in cancer treatment, offering new hope to patients with refractory or relapsed malignancies. By genetically modifying T lymphocytes, this potent method allows for the targeted eradication of infectious cells. The efficient production of CAR-T cells is essential for the effective use of these treatments to treat malignancies, as it affects not just the product's efficacy as well as safety but also its general availability to patients who require it. This article's primary goal is to provide a comprehensive overview of CAR-T therapy, encompassing its historical evolution, mechanistic insights, clinical applications, challenges, and future directions. By synthesizing existing literature and real-world evidence, this review seeks to elucidate the significance of CAR-T therapy in the landscape of cancer treatment and its potential to redefine the standard of care for patients with refractory or relapsed malignancies. The methodology involved a comprehensive literature search conducted using various databases, including PubMed, Google Scholar, and clinical trial registries such as ClinicalTrials.gov. The search strategy incorporated a combination of relevant keywords and Medical Subject Headings (MeSH) terms, including but not limited to "CAR-T therapy," "chimeric antigen receptor T-cell therapy," "cancer immunotherapy," "clinical trials," "pharmaceutical companies," "regulatory approvals," "pipeline molecules," and "cancer types." Boolean operators (AND, OR) were utilized to refine the search and capture relevant articles and studies. In addition to database searches, manual screening of reference lists from relevant review articles and primary studies was performed to identify additional relevant publications. The inclusion criteria encompassed original research articles, clinical trials, systematic reviews, meta-analyses, and regulatory documents related to CAR-T cell therapy and its applications in cancer treatment and the review included studies published in English between January 2010 and March 2024. Exclusion criteria comprised studies not relevant to the scope of the review, such as those focusing on non-CAR-T cell therapies or non-cancer-related topics. This review underscores the transformative potential of CAR-T therapy in cancer treatment, highlighting its efficacy, safety, and clinical relevance across various malignancies. By synthesizing findings from preclinical studies, clinical trials, and real-world data from patients, CAR-T therapy has consistently exhibited remarkable therapeutic outcomes. These include high response rates, durable remissions, and significant improvements in survival outcomes among patients with refractory or relapsed cancers. Additionally, the inclusion of practical research with big data from real patients further supports the robustness and applicability of CAR-T therapy in clinical practice. In conclusion, CAR-T therapy represents a paradigm shift in cancer treatment, offering new avenues for personalized and precision-driven oncology. By addressing current gaps, optimizing treatment protocols, and exploring novel strategies, CAR-T therapy holds immense promise in reshaping the landscape of oncology and providing hope to patients with advanced malignancies.
引用
收藏
页数:10
相关论文
共 58 条
[1]   A Novel Chimeric Antigen Receptor Against Prostate Stem Cell Antigen Mediates Tumor Destruction in a Humanized Mouse Model of Pancreatic Cancer [J].
Abate-Daga, Daniel ;
Lagisetty, Kiran H. ;
Tran, Eric ;
Zheng, Zhili ;
Gattinoni, Luca ;
Yu, Zhiya ;
Burns, William R. ;
Miermont, Anne M. ;
Teper, Yaroslav ;
Rudloff, Udo ;
Restifo, Nicholas P. ;
Feldman, Steven A. ;
Rosenberg, Steven A. ;
Morgan, Richard A. .
HUMAN GENE THERAPY, 2014, 25 (12) :1003-1012
[2]  
Ahmadiankia N., 2021, Eur. J. Pharmacol, V899, P174072, DOI [10.1016/j.ejphar.2020.174072, DOI 10.1016/J.EJPHAR.2020.174072]
[3]   Function of Novel Anti-CD19 Chimeric Antigen Receptors with Human Variable Regions Is Affected by Hinge and Transmembrane Domains [J].
Alabanza, Leah ;
Pegues, Melissa ;
Geldres, Claudia ;
Shi, Victoria ;
Wiltzius, Jed J. W. ;
Sievers, Stuart A. ;
Yang, Shicheng ;
Kochenderfer, James N. .
MOLECULAR THERAPY, 2017, 25 (11) :2452-2465
[4]   Inclusion of an IgG1-Fc spacer abrogates efficacy of CD19 CAR T cells in a xenograft mouse model [J].
Almasbak, H. ;
Walseng, E. ;
Kristian, A. ;
Myhre, M. R. ;
Suso, E. M. ;
Munthe, L. A. ;
Andersen, J. T. ;
Wang, M. Y. ;
Kvalheim, G. ;
Gaudernack, G. ;
Kyte, J. A. .
GENE THERAPY, 2015, 22 (05) :391-403
[5]  
[Anonymous], 2024, Brown-Forsythe test
[6]  
[Anonymous], 2019, W.O. Patent, Patent No. [2019210293A1, 2019210293]
[7]  
[Anonymous], 2017, K.R. Patent, Patent No. [102546839B1, 102546839]
[8]  
[Anonymous], 2018, U.S. Patent, Patent No. [11759480B2, 11759480]
[9]  
[Anonymous], 2018, C.N. Patent, Patent No. [114144430B, 114144430]
[10]  
[Anonymous], ?About us"