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Inotuzumab ozogamicin for the treatment of acute lymphoblastic leukemia
Therapy for adult acute lymphoblastic leukemia (ALL) with multiagent cytotoxic chemotherapy has not been as successful as that for pediatric patients. The advent of targeted monoclonal antibodies against common cell surface antigens (i.e. CD19, CD20, and CD22) has resulted in improved outcomes witho...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992772/ https://www.ncbi.nlm.nih.gov/pubmed/33815734 http://dx.doi.org/10.1177/2040620718812013 |
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author | Savoy, J. Michael Welch, Mary Alma Nasnas, Patrice E. Kantarjian, Hagop Jabbour, Elias |
author_facet | Savoy, J. Michael Welch, Mary Alma Nasnas, Patrice E. Kantarjian, Hagop Jabbour, Elias |
author_sort | Savoy, J. Michael |
collection | PubMed |
description | Therapy for adult acute lymphoblastic leukemia (ALL) with multiagent cytotoxic chemotherapy has not been as successful as that for pediatric patients. The advent of targeted monoclonal antibodies against common cell surface antigens (i.e. CD19, CD20, and CD22) has resulted in improved outcomes without additional toxicities. Inotuzumab ozogamicin is an anti-CD22 antibody–drug conjugate approved for the treatment of relapsed or refractory B-cell precursor ALL. It improved outcomes compared with standard salvage chemotherapy. Its combination with low-intensity chemotherapy in the relapse setting and in frontline elderly patients is promising. |
format | Online Article Text |
id | pubmed-7992772 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-79927722021-04-02 Inotuzumab ozogamicin for the treatment of acute lymphoblastic leukemia Savoy, J. Michael Welch, Mary Alma Nasnas, Patrice E. Kantarjian, Hagop Jabbour, Elias Ther Adv Hematol Review Therapy for adult acute lymphoblastic leukemia (ALL) with multiagent cytotoxic chemotherapy has not been as successful as that for pediatric patients. The advent of targeted monoclonal antibodies against common cell surface antigens (i.e. CD19, CD20, and CD22) has resulted in improved outcomes without additional toxicities. Inotuzumab ozogamicin is an anti-CD22 antibody–drug conjugate approved for the treatment of relapsed or refractory B-cell precursor ALL. It improved outcomes compared with standard salvage chemotherapy. Its combination with low-intensity chemotherapy in the relapse setting and in frontline elderly patients is promising. SAGE Publications 2018-11-22 /pmc/articles/PMC7992772/ /pubmed/33815734 http://dx.doi.org/10.1177/2040620718812013 Text en © The Author(s), 2018 http://www.creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (http://www.creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Review Savoy, J. Michael Welch, Mary Alma Nasnas, Patrice E. Kantarjian, Hagop Jabbour, Elias Inotuzumab ozogamicin for the treatment of acute lymphoblastic leukemia |
title | Inotuzumab ozogamicin for the treatment of acute lymphoblastic leukemia |
title_full | Inotuzumab ozogamicin for the treatment of acute lymphoblastic leukemia |
title_fullStr | Inotuzumab ozogamicin for the treatment of acute lymphoblastic leukemia |
title_full_unstemmed | Inotuzumab ozogamicin for the treatment of acute lymphoblastic leukemia |
title_short | Inotuzumab ozogamicin for the treatment of acute lymphoblastic leukemia |
title_sort | inotuzumab ozogamicin for the treatment of acute lymphoblastic leukemia |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992772/ https://www.ncbi.nlm.nih.gov/pubmed/33815734 http://dx.doi.org/10.1177/2040620718812013 |
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