Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2018 Mar;13(1):27-31.
doi: 10.1159/000486706. Epub 2018 Feb 20.

Checkpoint Inhibitors in Breast Cancer - Current Status and Future Directions

Affiliations
Review

Checkpoint Inhibitors in Breast Cancer - Current Status and Future Directions

Joachim Bischoff. Breast Care (Basel). 2018 Mar.

Abstract

Antineoplastic agents directly targeting tumor cells have represented the major strategy of systemic anticancer therapy for many years. Nevertheless, overcoming resistance mechanisms remains a great challenge because treatment options are limited in many cases. From this point of view, immunotherapeutic approaches seem promising in a broad spectrum of solid tumors. These include in particular the currently available inhibitors directed against immune checkpoints leading to a significant T-cell activation. To date, the programmed death receptor 1 (PD-1) and its ligand are the most prominent targets in this context. However, the role of checkpoint inhibitors in the treatment of breast cancer is still being debated, and the main focus is on triple-negative breast cancer patients as a target population in many ongoing trials. Moreover, the potential superiority of combinations with other anticancer drugs such as cytotoxics and targeted agents will be discussed.

Keywords: Checkpoint inhibitors; Expression; Immune oncology; Monoclonal antibodies; PD-1/PD-L1 system; Triple-negative breast cancer.

PubMed Disclaimer

References

    1. Yao S, Zhu Y, Chen L. Advances in targeting cell surface sigalling molecules for immune modulation. Nat Ref Drug Discov. 2013;12:130–146. - PMC - PubMed
    1. Brunet JF, Denizot F, Lucianni MF, et al. A new member of the immunoglobulin superfamily - CTLA-4. Nature. 1987;328:267–270. - PubMed
    1. Chemnitz JM, Parry RV, Nichols KE, et al. SHP-1 and SHP-2 associate with immunoreceptor tyrosine-based switch motif of programmed death 1 upon primary human T cell stimulation, but only receptor ligation prevents T cell activation. J Immunol. 2004;173:945–954. - PubMed
    1. Pardoll DM. The blockade of immune checkpoints in cancer immunotherapy. Nat Rev Cancer. 2012;12:252–264. - PMC - PubMed
    1. Sage PT, Francisco LM, Carman CV, Shape AH. The receptor PD-1 controls follicular regulatory T cells in the lymph nodes and blood. Nat Immunol. 2013;14:152–181. - PMC - PubMed