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Novel agents and biomarkers for acute lymphoid leukemia

New genetic markers for adult acute lymphoblastic leukemia (ALL) have been found to have prognostic impact, such as the lymphoid transcription factor gene IKZF1 alterations, which are associated with a high rate of leukemic relapse in B-ALL. Although complete remission rates by induction chemotherap...

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Detalles Bibliográficos
Autores principales: Zhao, Yanmin, Huang, He, Wei, Guoqing
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3718656/
https://www.ncbi.nlm.nih.gov/pubmed/23773228
http://dx.doi.org/10.1186/1756-8722-6-40
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author Zhao, Yanmin
Huang, He
Wei, Guoqing
author_facet Zhao, Yanmin
Huang, He
Wei, Guoqing
author_sort Zhao, Yanmin
collection PubMed
description New genetic markers for adult acute lymphoblastic leukemia (ALL) have been found to have prognostic impact, such as the lymphoid transcription factor gene IKZF1 alterations, which are associated with a high rate of leukemic relapse in B-ALL. Although complete remission rates by induction chemotherapy in ALL are now high, the long-term survival is still disappointing. Improvements in the survival outcome of ALL have been observed in young adults as a result of the use of pediatric inspired regimens and the broadening of the number of patients who are eligible for allogeneic SCT. Development of new and less toxic agents also provide promise to improve the outcome in adult ALL, such as tyrosine kinase inhibitors in Ph-positive ALL, rituximab in CD20-positive disease, blinatumomab in precursor B-ALL and nelarabine in T-lineage ALL. Challenges for the future are to implement genomic profiling into the clinical setting to guide risk stratification and providing novel targets for tailored therapies.
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spelling pubmed-37186562013-07-23 Novel agents and biomarkers for acute lymphoid leukemia Zhao, Yanmin Huang, He Wei, Guoqing J Hematol Oncol Review New genetic markers for adult acute lymphoblastic leukemia (ALL) have been found to have prognostic impact, such as the lymphoid transcription factor gene IKZF1 alterations, which are associated with a high rate of leukemic relapse in B-ALL. Although complete remission rates by induction chemotherapy in ALL are now high, the long-term survival is still disappointing. Improvements in the survival outcome of ALL have been observed in young adults as a result of the use of pediatric inspired regimens and the broadening of the number of patients who are eligible for allogeneic SCT. Development of new and less toxic agents also provide promise to improve the outcome in adult ALL, such as tyrosine kinase inhibitors in Ph-positive ALL, rituximab in CD20-positive disease, blinatumomab in precursor B-ALL and nelarabine in T-lineage ALL. Challenges for the future are to implement genomic profiling into the clinical setting to guide risk stratification and providing novel targets for tailored therapies. BioMed Central 2013-06-18 /pmc/articles/PMC3718656/ /pubmed/23773228 http://dx.doi.org/10.1186/1756-8722-6-40 Text en Copyright © 2013 Zhao et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review
Zhao, Yanmin
Huang, He
Wei, Guoqing
Novel agents and biomarkers for acute lymphoid leukemia
title Novel agents and biomarkers for acute lymphoid leukemia
title_full Novel agents and biomarkers for acute lymphoid leukemia
title_fullStr Novel agents and biomarkers for acute lymphoid leukemia
title_full_unstemmed Novel agents and biomarkers for acute lymphoid leukemia
title_short Novel agents and biomarkers for acute lymphoid leukemia
title_sort novel agents and biomarkers for acute lymphoid leukemia
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3718656/
https://www.ncbi.nlm.nih.gov/pubmed/23773228
http://dx.doi.org/10.1186/1756-8722-6-40
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