Chimeric antigen receptor-based immunotherapy in breast cancer: Recent progress in China

被引:2
|
作者
Yu, Tianze [1 ,2 ,7 ]
Lu, Yuexin [1 ,2 ]
Fang, Jianwen [1 ,2 ]
Jiang, Xiaocong [1 ,2 ]
Lu, Yue [3 ]
Zheng, Jingyan [4 ]
Shang, Xi [5 ]
Shen, Haixing [6 ]
Fu, Peifen [1 ,7 ]
机构
[1] Zhejiang Univ, Affiliated Hosp 1, Sch Med, Dept Breast Surg, Hangzhou, Peoples R China
[2] Zhejiang Univ, Sch Med, Hangzhou, Peoples R China
[3] Huzhou Univ, Affiliated Hosp 1, Dept Breast & Thyroid Surg, Huzhou, Peoples R China
[4] Wenzhou Med Univ, Affiliated Hosp 6, Lishui Peoples Hosp, Dept Breast & Thyroid Surg, Lishui, Peoples R China
[5] Zhejiang Univ, Taizhou Hosp, Dept Breast & Thyroid Surg, Taizhou, Peoples R China
[6] Cixi Peoples Hosp, Dept Breast & Thyroid Surg, Cixi, Peoples R China
[7] Zhejiang Univ, Affiliated Hosp 1, Sch Med, Dept Breast Surg, Hangzhou 310003, Peoples R China
关键词
breast cancer; chimeric antigen receptor; immunotherapy; macrophages; natural killer cells; T cells; CAR-T-CELLS; NATURAL-KILLER-CELLS; THERAPY; MESOTHELIN; RADIATION; EFFICACY; LYMPHOCYTES; SUPPRESSION; EXPRESSION; IMPROVE;
D O I
10.1002/cncr.35096
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Breast cancer (BC) is the fourth most prevalent cancer in China. Despite conventional treatment strategies, BC patients often have poor therapeutic outcomes, leading to significant global cancer mortality rates. Chimeric antigen receptor (CAR)-based immunotherapy is a promising and innovative approach for cancer treatment that redirects immune cells to attack tumor cells expressing selected tumor antigens (TAs). T cells, natural killer (NK) cells, and macrophages, key components of the immune system, are used in CAR-based immunotherapies. Although remarkable progress has been made with CAR-T cells in hematologic malignancies, the application of CAR-based immunotherapy to BC has lagged. This is partly due to obstacles such as tumor heterogeneity, which is further associated with the TA and BC subtypes, and the immunosuppressive tumor microenvironment (TME). Several combinatorial approaches, including the use of immune checkpoint inhibitors, oncolytic viruses, and antitumor drugs, have been proposed to overcome these obstacles in BC treatment. Furthermore, several CAR-based immunotherapies for BC have been translated into clinical trials. This review provides an overview of the recent progress in CAR-based immunotherapy for BC treatment, including targeting of TAs, consideration of BC subtypes, assessment of the TME, and exploration of combinatorial therapies. The authors focused on preclinical studies and clinical trials of CAR-T cells, CAR-NK cells, and CAR-macrophages especially conducted in China, followed by an internal comparison and discussion of current limits. In conclusion, this review elucidates China's contribution to CAR-based immunotherapies for BC and provides inspiration for further research.Plain Language SummaryDespite conventional treatment strategies, breast cancer (BC) patients in China often have poor therapeutic outcomes.Chimeric antigen receptor (CAR)-based immunotherapy, a promising approach, can redirect immune cells to kill tumor cells expressing selected tumor antigens (TAs). However, obstacles such as TA selection, BC subtypes, and immunosuppressive tumor microenvironment still exist. Therefore, various combinatorial approaches have been proposed.This article elucidates several Chinese CAR-based preclinical and clinical studies in BC treatment with comparisons of foreign research, and CAR-immune cells are analyzed, providing inspiration for further research. This review elucidates China's contribution to chimeric antigen receptor (CAR)-based immunotherapies for breast cancer including preclinical research and clinical trials. The article further makes comparisons between each CAR-based immunotherapy and provides inspirations for further research.
引用
收藏
页码:1378 / 1391
页数:14
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