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CAR T-cell therapy for triple-negative breast cancer: Where we are.
- Source :
-
Cancer letters [Cancer Lett] 2020 Oct 28; Vol. 491, pp. 121-131. Date of Electronic Publication: 2020 Aug 12. - Publication Year :
- 2020
-
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.<br /> (Copyright © 2020 Elsevier B.V. All rights reserved.)
- Subjects :
- Antigens, Neoplasm immunology
Chondroitin Sulfate Proteoglycans immunology
Female
Folate Receptor 1 immunology
GPI-Linked Proteins immunology
Humans
Immunotherapy, Adoptive adverse effects
Intercellular Adhesion Molecule-1 immunology
Membrane Proteins immunology
Mesothelin
Mucin-1 immunology
NK Cell Lectin-Like Receptor Subfamily K immunology
Receptor Tyrosine Kinase-like Orphan Receptors immunology
Immunotherapy, Adoptive methods
Triple Negative Breast Neoplasms therapy
Subjects
Details
- Language :
- English
- ISSN :
- 1872-7980
- Volume :
- 491
- Database :
- MEDLINE
- Journal :
- Cancer letters
- Publication Type :
- Academic Journal
- Accession number :
- 32795486
- Full Text :
- https://doi.org/10.1016/j.canlet.2020.07.044