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Management of adverse effects of new monoclonal antibody treatments in acute lymphoblastic leukemia
Therapeutic options for relapsed/refractory B-cell acute lymphoblastic leukemia have evolved in the past few years. The FDA has approved three novel therapies for this disease: inotuzumab ozogamicin (an anti-CD22 antibody–drug conjugate), blinatumomab (a bispecific T-cell engager), and chimeric anti...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioExcel Publishing Ltd
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7560100/ https://www.ncbi.nlm.nih.gov/pubmed/33110433 http://dx.doi.org/10.7573/dic.2020-7-2 |
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author | Conde-Royo, Diego Juárez-Salcedo, Luis Miguel Dalia, Samir |
author_facet | Conde-Royo, Diego Juárez-Salcedo, Luis Miguel Dalia, Samir |
author_sort | Conde-Royo, Diego |
collection | PubMed |
description | Therapeutic options for relapsed/refractory B-cell acute lymphoblastic leukemia have evolved in the past few years. The FDA has approved three novel therapies for this disease: inotuzumab ozogamicin (an anti-CD22 antibody–drug conjugate), blinatumomab (a bispecific T-cell engager), and chimeric antigen receptor T-cell therapy. Although these novel immunotherapies have revolutionized the therapeutic landscape, it is important to understand the crucial aspects of administration, especially toxicity. In this article, we review the unique toxicities and adverse effects of blinatumomab and inotuzumab ozogamicin and provide recommendations for prevention of adverse effects as well as the management options for each medication. |
format | Online Article Text |
id | pubmed-7560100 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioExcel Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-75601002020-10-26 Management of adverse effects of new monoclonal antibody treatments in acute lymphoblastic leukemia Conde-Royo, Diego Juárez-Salcedo, Luis Miguel Dalia, Samir Drugs Context Review Therapeutic options for relapsed/refractory B-cell acute lymphoblastic leukemia have evolved in the past few years. The FDA has approved three novel therapies for this disease: inotuzumab ozogamicin (an anti-CD22 antibody–drug conjugate), blinatumomab (a bispecific T-cell engager), and chimeric antigen receptor T-cell therapy. Although these novel immunotherapies have revolutionized the therapeutic landscape, it is important to understand the crucial aspects of administration, especially toxicity. In this article, we review the unique toxicities and adverse effects of blinatumomab and inotuzumab ozogamicin and provide recommendations for prevention of adverse effects as well as the management options for each medication. BioExcel Publishing Ltd 2020-10-14 /pmc/articles/PMC7560100/ /pubmed/33110433 http://dx.doi.org/10.7573/dic.2020-7-2 Text en Copyright © 2020 Mittal SO. Published by Drugs in Context under Creative Commons License Deed CC BY NC ND 4.0 which allows anyone to copy, distribute, and transmit the article provided it is properly attributed in the manner specified below. No commercial use without permission. |
spellingShingle | Review Conde-Royo, Diego Juárez-Salcedo, Luis Miguel Dalia, Samir Management of adverse effects of new monoclonal antibody treatments in acute lymphoblastic leukemia |
title | Management of adverse effects of new monoclonal antibody treatments in acute lymphoblastic leukemia |
title_full | Management of adverse effects of new monoclonal antibody treatments in acute lymphoblastic leukemia |
title_fullStr | Management of adverse effects of new monoclonal antibody treatments in acute lymphoblastic leukemia |
title_full_unstemmed | Management of adverse effects of new monoclonal antibody treatments in acute lymphoblastic leukemia |
title_short | Management of adverse effects of new monoclonal antibody treatments in acute lymphoblastic leukemia |
title_sort | management of adverse effects of new monoclonal antibody treatments in acute lymphoblastic leukemia |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7560100/ https://www.ncbi.nlm.nih.gov/pubmed/33110433 http://dx.doi.org/10.7573/dic.2020-7-2 |
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