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Cleavable linkers in antibody–drug conjugates.

Authors :
Bargh, Jonathan D.
Isidro-Llobet, Albert
Parker, Jeremy S.
Spring, David R.
Source :
Chemical Society Reviews; 8/21/2019, Vol. 48 Issue 16, p4361-4374, 14p
Publication Year :
2019

Abstract

Antibody–Drug Conjugates (ADCs) are now established as a major class of therapeutics for the clinical treatment of cancer. The properties of the linker between the antibody and the payload are proven to be critical to the success of an ADC. Although ADC linkers can be 'non-cleavable', the vast majority of ADCs in clinical development have specific release mechanisms to allow controlled linker cleavage at the target site and are thus termed 'cleavable'. In recent years, the development of new methods of drug release from ADCs has continued in parallel to the deepening understanding of the biological processes underlying the mechanisms of action of pre-existing technologies. This review summarises the advances in the field of cleavable linker technologies for ADCs. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03060012
Volume :
48
Issue :
16
Database :
Complementary Index
Journal :
Chemical Society Reviews
Publication Type :
Academic Journal
Accession number :
138030622
Full Text :
https://doi.org/10.1039/c8cs00676h