| Literature DB >> 32795486 |
Yuetao Xie1, Yi Hu1, Nawu Zhou1, Cuicui Yao1, Lixin Wu1, Lin Liu2, Fang Chen3.
Abstract
Triple-negative breast cancer (TNBC) is the most complex and challenging breast cancer subtype to treat, and chemotherapy remains the standard of care. Clinically, TNBC has a relatively high rate of recurrence and poor prognosis, which leads to a significant effort to discover novel strategies to treat patients with these tumors. Currently, chimeric antigen receptor (CAR) T cell-based immunotherapy redirects the patient's immune system directly to recognize and eradicate tumor-associated antigens (TAAs) expressing tumor cells being explored as a treatment for TNBC. A steadily increasing research in CAR T-cell therapy targeting different TAAs in TNBC has reported. In this review, we introduce the CAR technology and summarize the potential TAAs, available CARs, the antitumor activity, and the related toxicity of CARs currently under investigation for TNBC. We also highlight the potential strategies to prevent/reduce potential "on target, off tumor" toxicity induced by CAR T-cell therapy. This review will help to explore proper targets to expand further the CAR T-cell therapy for TNBCs in the clinic.Entities:
Keywords: Chimeric antigen receptor; Immunotherapy; T cells; Triple-negative breast cancer; Tumor antigens
Year: 2020 PMID: 32795486 DOI: 10.1016/j.canlet.2020.07.044
Source DB: PubMed Journal: Cancer Lett ISSN: 0304-3835 Impact factor: 8.679