Antibody-drug conjugates in solid tumors: a look into novel targets
- PMID: 33509252
- PMCID: PMC7844898
- DOI: 10.1186/s13045-021-01035-z
Antibody-drug conjugates in solid tumors: a look into novel targets
Abstract
Antibody-drug conjugates (ADCs) are a relatively new class of anticancer agents designed to merge the selectivity of monoclonal antibodies with cell killing properties of chemotherapy. They are commonly described as the "Trojan Horses" of therapeutic armamentarium, because of their capability of directly conveying cytotoxic drug (payloads) into the tumor space, thus transforming chemotherapy into a targeted agent. Three novel ADCs have been recently approved, i.e., trastuzumab deruxtecan, sacituzumab govitecan and enfortumab vedotin, respectively, targeting HER2, Trop2 and Nectin4. Thanks to progressive advances in engineering technologies these drugs rely on, the spectrum of diseases sensitive to these drugs as well as their indications are in continuous expansion. Several novel ADCs are under evaluation, exploring new potential targets along with innovative payloads. This review aims at providing a summary of the technology behind these compounds and at presenting the latest ADCs approved in solid tumors, as well as at describing novel targets for ADCs under investigation and new strategies to optimize their efficacy in solid tumors.
Keywords: ADCs; Antibody–drug conjugates; Cancer; Solid tumors.
Conflict of interest statement
CC has received honoraria for consultancy/advisory role/speaker bureau from Pfizer, Lilly, Novartis, Roche, all outside the submitted work. SM has no potential conflicts of interest to disclose. GC served as consultant or advisor for Roche, Lilly, and Bristol-Myers Squibb, served on the speaker’s bureau for Roche, Pfizer, and Lilly, received travel funding from Pfizer and Roche, and received honoraria from Roche, Pfizer, Lilly, Novartis, and SEAGEN.
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