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Gemtuzumab Ozogamicin: Back Again

Despite the recent onslaught of approved medications in oncology, acute myeloid leukemia (AML) has been a disease state bereft of pharmaceutical development for decades. The long-standing first-line regimen, 7 + 3, was developed in 1973. A group of four physicians at Roswell Park Memorial Institute...

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Autores principales: Selby, Chris, Yacko, Lisa R., Glode, Ashley E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Harborside Press 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6605703/
https://www.ncbi.nlm.nih.gov/pubmed/31308990
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author Selby, Chris
Yacko, Lisa R.
Glode, Ashley E.
author_facet Selby, Chris
Yacko, Lisa R.
Glode, Ashley E.
author_sort Selby, Chris
collection PubMed
description Despite the recent onslaught of approved medications in oncology, acute myeloid leukemia (AML) has been a disease state bereft of pharmaceutical development for decades. The long-standing first-line regimen, 7 + 3, was developed in 1973. A group of four physicians at Roswell Park Memorial Institute built upon prior combinations of daunorubicin and cytarabine to find the optimal combination of 7 days of cytarabine and 3 days of daunorubicin (Lichtman, 2013). This regimen has undergone multiple modifications and patient performance status-based stratifications, but has remained the first-line therapy for AML for the past 45 years. In September 2017, gemtuzumab ozogamicin returned to market and shortly thereafter was added to the National Comprehensive Cancer Network (NCCN) Clinical Practice Guidelines for AML, to be administered in combination with 7 + 3, and as monotherapy for both newly diagnosed and relapsed patients with acute myeloid leukemia (NCCN, 2018; US Food & Drug Administration, 2017). Gemtuzumab ozogamicin continues to be explored in various leukemia settings and is a welcomed addition to the currently available treatment options for AML.
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spelling pubmed-66057032019-07-15 Gemtuzumab Ozogamicin: Back Again Selby, Chris Yacko, Lisa R. Glode, Ashley E. J Adv Pract Oncol Review Article Despite the recent onslaught of approved medications in oncology, acute myeloid leukemia (AML) has been a disease state bereft of pharmaceutical development for decades. The long-standing first-line regimen, 7 + 3, was developed in 1973. A group of four physicians at Roswell Park Memorial Institute built upon prior combinations of daunorubicin and cytarabine to find the optimal combination of 7 days of cytarabine and 3 days of daunorubicin (Lichtman, 2013). This regimen has undergone multiple modifications and patient performance status-based stratifications, but has remained the first-line therapy for AML for the past 45 years. In September 2017, gemtuzumab ozogamicin returned to market and shortly thereafter was added to the National Comprehensive Cancer Network (NCCN) Clinical Practice Guidelines for AML, to be administered in combination with 7 + 3, and as monotherapy for both newly diagnosed and relapsed patients with acute myeloid leukemia (NCCN, 2018; US Food & Drug Administration, 2017). Gemtuzumab ozogamicin continues to be explored in various leukemia settings and is a welcomed addition to the currently available treatment options for AML. Harborside Press 2019 2019-01-01 /pmc/articles/PMC6605703/ /pubmed/31308990 Text en Copyright © 2019, Harborside Press http://creativecommons.org/licenses/by-nc/3.0/ This article is distributed under the terms of the Creative Commons Attribution Non-Commercial License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Selby, Chris
Yacko, Lisa R.
Glode, Ashley E.
Gemtuzumab Ozogamicin: Back Again
title Gemtuzumab Ozogamicin: Back Again
title_full Gemtuzumab Ozogamicin: Back Again
title_fullStr Gemtuzumab Ozogamicin: Back Again
title_full_unstemmed Gemtuzumab Ozogamicin: Back Again
title_short Gemtuzumab Ozogamicin: Back Again
title_sort gemtuzumab ozogamicin: back again
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6605703/
https://www.ncbi.nlm.nih.gov/pubmed/31308990
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