dc.creatorZhao, Pengxuan
dc.creatorZhang, Yuebao
dc.creatorLi, Wenqing
dc.creatorJeanty, Christopher
dc.creatorXiang, Guangya
dc.date.accessioned2020-07-23T14:50:12Z
dc.date.accessioned2022-09-23T18:20:13Z
dc.date.available2020-07-23T14:50:12Z
dc.date.available2022-09-23T18:20:13Z
dc.date.created2020-07-23T14:50:12Z
dc.identifierhttps://doi.org/10.1016/j.apsb.2020.04.012
dc.identifierhttp://hdl.handle.net/20.500.12010/11019
dc.identifierhttps://doi.org/10.1016/j.apsb.2020.04.012
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3499057
dc.description.abstractAntibody drug conjugates (ADCs) normally compose of a humanized antibody and small molecular drug via a chemical linker. After decades of preclinical and clinical studies, a series of ADCs have been widely used for treating specific tumor types in the clinic such as brentuximab vedotin (Adcetris® ) for relapsed Hodgkin’s lymphoma and systemic anaplastic large cell lymphoma, gemtuzumab ozogamicin (Mylotarg® ) for acute myeloid leukemia, ado-trastuzumab emtansine (Kadcyla® ) for HER2-positive metastatic breast cancer, inotuzumab ozogamicin (Besponsa® ) and most recently polatuzumab vedotin-piiq (Polivy ® ) for B cell malignancies. More than eighty ADCs have been investigated in different clinical stages from approximately six hundred clinical trials to date. This review summarizes the key elements of ADCs and highlights recent advances of ADCs, as well as important lessons learned from clinical data, and future directions.
dc.publisherScience Direct
dc.rightsinfo:eu-repo/semantics/openAccess
dc.sourcereponame:Expeditio Repositorio Institucional UJTL
dc.sourceinstname:Universidad de Bogotá Jorge Tadeo Lozano
dc.subjectAntibody drug conjugates
dc.subjectAntibody
dc.subjectCytotoxic agents
dc.subjectLinker
dc.subjectClinical application
dc.titleRecent advances of antibody drug conjugates for clinical applications


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