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Antibody-drug conjugates in clinical trials for lymphoid malignancies and multiple myeloma

Antibody-drug conjugates (ADC) represent a distinct family of chemoimmunotherapy agents. ADCs are composed of monoclonal antibodies conjugated to cytotoxic payloads via specialized chemical linkers. ADCs therefore combine the immune therapy with targeted chemotherapy. Due to the distinct biomarkers...

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Detalles Bibliográficos
Autores principales: Yu, Bo, Liu, Delong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6734251/
https://www.ncbi.nlm.nih.gov/pubmed/31500657
http://dx.doi.org/10.1186/s13045-019-0786-6
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author Yu, Bo
Liu, Delong
author_facet Yu, Bo
Liu, Delong
author_sort Yu, Bo
collection PubMed
description Antibody-drug conjugates (ADC) represent a distinct family of chemoimmunotherapy agents. ADCs are composed of monoclonal antibodies conjugated to cytotoxic payloads via specialized chemical linkers. ADCs therefore combine the immune therapy with targeted chemotherapy. Due to the distinct biomarkers associated with lymphocytes and plasma cells, ADCs have emerged as a promising treatment option for lymphoid malignancies and multiple myeloma. Several ADCs have been approved for clinical applications: brentuximab vedotin, inotuzumab ozogamicin, moxetumomab pasudotox, and polatuzumab vedotin. More novel ADCs are under clinical development. In this article, we summarized the general principles for ADC design, and updated novel ADCs under various stages of clinical trials for lymphoid malignancies and multiple myeloma.
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spelling pubmed-67342512019-09-12 Antibody-drug conjugates in clinical trials for lymphoid malignancies and multiple myeloma Yu, Bo Liu, Delong J Hematol Oncol Review Antibody-drug conjugates (ADC) represent a distinct family of chemoimmunotherapy agents. ADCs are composed of monoclonal antibodies conjugated to cytotoxic payloads via specialized chemical linkers. ADCs therefore combine the immune therapy with targeted chemotherapy. Due to the distinct biomarkers associated with lymphocytes and plasma cells, ADCs have emerged as a promising treatment option for lymphoid malignancies and multiple myeloma. Several ADCs have been approved for clinical applications: brentuximab vedotin, inotuzumab ozogamicin, moxetumomab pasudotox, and polatuzumab vedotin. More novel ADCs are under clinical development. In this article, we summarized the general principles for ADC design, and updated novel ADCs under various stages of clinical trials for lymphoid malignancies and multiple myeloma. BioMed Central 2019-09-10 /pmc/articles/PMC6734251/ /pubmed/31500657 http://dx.doi.org/10.1186/s13045-019-0786-6 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Review
Yu, Bo
Liu, Delong
Antibody-drug conjugates in clinical trials for lymphoid malignancies and multiple myeloma
title Antibody-drug conjugates in clinical trials for lymphoid malignancies and multiple myeloma
title_full Antibody-drug conjugates in clinical trials for lymphoid malignancies and multiple myeloma
title_fullStr Antibody-drug conjugates in clinical trials for lymphoid malignancies and multiple myeloma
title_full_unstemmed Antibody-drug conjugates in clinical trials for lymphoid malignancies and multiple myeloma
title_short Antibody-drug conjugates in clinical trials for lymphoid malignancies and multiple myeloma
title_sort antibody-drug conjugates in clinical trials for lymphoid malignancies and multiple myeloma
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6734251/
https://www.ncbi.nlm.nih.gov/pubmed/31500657
http://dx.doi.org/10.1186/s13045-019-0786-6
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