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MAbs. 2016 May-Jun;8(4):659-71. doi: 10.1080/19420862.2016.1156829. Epub 2016 Apr 5.

Effects of antibody, drug and linker on the preclinical and clinical toxicities of antibody-drug conjugates.

Author information

1
a Hanson Wade , 52 Grosvenor Gardens, London , UK.

Abstract

Antibody-drug conjugates (ADCs) represent a new class of cancer therapeutics. Their design involves a tumor-specific antibody, a linker and a cytotoxic payload. They were designed to allow specific targeting of highly potent cytotoxic agents to tumor cells whilst sparing normal cells. Frequent toxicities that may be driven by any of the components of an ADC have been reported. There are currently more than 50 ADCs in active clinical development, and a further ∼20 that have been discontinued. For this review, the reported toxicities of ADCs were analysed, and the mechanisms for their effects are explored in detail. Methods to reduce toxicities, including dosing strategies and drug design, are discussed. The toxicities reported for active and discontinued drugs are important to drive the rational design and improve the therapeutic index of ADCs of the future.

KEYWORDS:

ADC; Antibody-drug conjugate; clinical trials; payload; therapeutic index; toxicity

PMID:
27045800
PMCID:
PMC4966843
DOI:
10.1080/19420862.2016.1156829
[Indexed for MEDLINE]
Free PMC Article

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