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

被引:120
作者
Conilh, Louise [1 ,2 ]
Sadilkova, Lenka [2 ]
Viricel, Warren [2 ]
Dumontet, Charles [1 ,3 ]
机构
[1] Univ Lyon, Canc Res Ctr Lyon, UMR INSERM 1052, CNRS 5286, Lyon, France
[2] Mablink Biosci, Lyon, France
[3] Hosp Civils Lyon, Lyon, France
关键词
Antibody-drug conjugates; Payload; Topoisomerase; 1; inhibitor; Cytotoxic molecule; TOPOISOMERASE-I INHIBITOR; RNA-POLYMERASE-II; MONOCLONAL-ANTIBODY; ANTITUMOR-ACTIVITY; VIVO TOXICITY; PHASE-II; PHARMACOKINETIC FEATURES; TRASTUZUMAB DERUXTECAN; GEMTUZUMAB OZOGAMICIN; BIOLOGICAL EVALUATION;
D O I
10.1186/s13045-022-01397-y
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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((R))) and sacituzumab govitecan (Trodelvy((R))), 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.
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页数:28
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