4.7 Review

Novel chimeric antigen receptor T cell-based immunotherapy: a perspective for triple-negative breast cancer

Journal

Publisher

FRONTIERS MEDIA SA
DOI: 10.3389/fcell.2023.1158539

Keywords

triple negative breast cancer; tumor antigens; immunotherapy; chimeric antigen receptors; radiotherapy

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Triple-negative breast cancer (TNBC) is a highly aggressive form of breast cancer that does not express certain receptors. Traditional therapies have limited efficacy against TNBC, and new treatment options are urgently needed. CAR-T therapy, a type of immunotherapy, has shown success in hematological cancers but has limitations in solid tumors like TNBC. This review explores the potential of CAR-T therapy in TNBC treatment, identifies therapeutic targets, and discusses strategies to overcome limitations and improve efficacy.
Triple-negative breast cancer (TNBC) is highly aggressive and does not express estrogen receptor (ER), progesterone (PR), or human epidermal growth factor receptor 2 (HER2). It has a poor prognosis, and traditional endocrine and anti-HER2 targeted therapies have low efficacy against it. In contrast, surgery, radiotherapy, and/or systemic chemotherapy are relatively effective at controlling TNBC. The resistance of TNBC to currently available clinical therapies has had a significantly negative impact on its treatment outcomes. Hence, new therapeutic options are urgently required. Chimeric antigen receptor T cell (CAR-T) therapy is a type of immunotherapy that integrates the antigen specificity of antibodies and the tumor-killing effect of T cells. CAR-T therapy has demonstrated excellent clinical efficacy against hematological cancers. However, its efficacy against solid tumors such as TNBC is inadequate. The present review aimed to investigate various aspects of CAR-T administration as TNBC therapy. We summarized the potential therapeutic targets of CAR-T that were identified in preclinical studies and clinical trials on TNBC. We addressed the limitations of using CAR-T in the treatment of TNBC in particular and solid tumors in general and explored key strategies to overcome these impediments. Finally, we comprehensively examined the advancement of CAR-T immunotherapy as well as countermeasures that could improve its efficacy as a TNBC treatment and the prognosis of patients with this type of cancer.

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