Development of small-molecule immune checkpoint inhibitors of PD-1/PD-L1 as a new therapeutic strategy for tumour immunotherapy
Cancer immunotherapy has been increasingly utilised to treat advanced malignancies. The signalling network of immune checkpoints has attracted considerable attention. Immune checkpoint inhibitors are revolutionising the treatment options and expectations for patients with cancer. The reported clinic...
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Published in | Journal of drug targeting Vol. 27; no. 3; pp. 244 - 256 |
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Main Authors | , |
Format | Journal Article |
Language | English |
Published |
England
Taylor & Francis
16.03.2019
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Subjects | |
Online Access | Get full text |
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Summary: | Cancer immunotherapy has been increasingly utilised to treat advanced malignancies. The
signalling network of immune checkpoints has attracted considerable attention. Immune
checkpoint inhibitors are revolutionising the treatment options and expectations for patients
with cancer. The reported clinical success of targeting the T-cell immune checkpoint receptors
PD-1/PD-L1 has demonstrated the importance of immune modulation. Indeed, antibodies binding to
PD-1 or PD-L1 have shown remarkable efficacy. However, antibody drugs have many disadvantages,
such as their production cost, stability, and immunogenicity and, therefore, small-molecule
inhibitors of PD-1 and its ligand PD-L1 are being introduced. Small-molecule inhibitors could
offer inherent advantages in terms of pharmacokinetics and druggability, thereby providing
additional methods for cancer treatment and achieving better therapeutic effects. In this
review, we first discuss how PD-1/PD-L1-targeting inhibitors modulate the relationship between
immune cells and tumour cells in tumour immunotherapy. Second, we discuss how the
immunomodulatory potential of these inhibitors can be exploited via rational combinations with
immunotherapy and targeted therapy. Third, this review is the first to summarise the current
clinical and preclinical evidence regarding small-molecule inhibitors of the PD-1/PD-L1 immune
checkpoint, considering features and responses related to the tumours and to the host immune
system.
Trial registration:
ClinicalTrials.gov identifier: NCT02812875. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 ObjectType-Review-3 content type line 23 |
ISSN: | 1061-186X 1029-2330 1029-2330 |
DOI: | 10.1080/1061186X.2018.1440400 |