Payload diversification: a key step in the development of antibody-drug conjugates

  • J Hematol Oncol. 2023 Jan 17;16(1):3. doi: 10.1186/s13045-022-01397-y.
Louise Conilh  1  2 Lenka Sadilkova  3 Warren Viricel  3 Charles Dumontet  4  5
Affiliations
  • 1. Cancer Research Center of Lyon, UMR INSERM 1052; CNRS 5286, University of Lyon, Lyon, France. [email protected].
  • 2. Mablink Bioscience, Lyon, France. [email protected].
  • 3. Mablink Bioscience, Lyon, France.
  • 4. Cancer Research Center of Lyon, UMR INSERM 1052; CNRS 5286, University of Lyon, Lyon, France.
  • 5. Hospices Civils de Lyon, Lyon, France.
Abstract

Antibody-drug conjugates (ADCs) is a fast moving class of targeted biotherapeutics that currently combines the selectivity of monoclonal antibodies with the potency of a payload consisting of cytotoxic agents. For many years microtubule targeting and DNA-intercalating agents were at the forefront of ADC development. The recent approval and clinical success of trastuzumab deruxtecan (Enhertu®) and sacituzumab govitecan (Trodelvy®), two Topoisomerase 1 inhibitor-based ADCs, has shown the potential of conjugating unconventional payloads with differentiated mechanisms of action. Among future developments in the ADC field, payload diversification is expected to play a key role as illustrated by a growing number of preclinical and clinical stage unconventional payload-conjugated ADCs. This review presents a comprehensive overview of validated, forgotten and newly developed payloads with different mechanisms of action.

Keywords
Antibody–drug conjugates; Cytotoxic molecule; Payload; Topoisomerase 1 inhibitor.
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