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Long lasting complete molecular remission after suspending dasatinib treatment in chronic myeloid leukemia

Tyrosine kinase inhibitors specific for BCR-ABL, were a major breakthrough in CML therapy. Second generation tyrosine kinase inhibitors (dasatinib, nilotinib) are indicated for imatinib resistant and intolerant patients. Present guidelines recommend continuous drug dosing for maintaining remission....

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Autores principales: Gadó, Klára, Matolcsy, András, Csomor, Judit, Kicsi, Dóra, Bödör, Csaba, Domján, Gyula
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3514089/
https://www.ncbi.nlm.nih.gov/pubmed/23210842
http://dx.doi.org/10.1186/2162-3619-1-17
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author Gadó, Klára
Matolcsy, András
Csomor, Judit
Kicsi, Dóra
Bödör, Csaba
Domján, Gyula
author_facet Gadó, Klára
Matolcsy, András
Csomor, Judit
Kicsi, Dóra
Bödör, Csaba
Domján, Gyula
author_sort Gadó, Klára
collection PubMed
description Tyrosine kinase inhibitors specific for BCR-ABL, were a major breakthrough in CML therapy. Second generation tyrosine kinase inhibitors (dasatinib, nilotinib) are indicated for imatinib resistant and intolerant patients. Present guidelines recommend continuous drug dosing for maintaining remission. There is no available data concerning the optimal duration of dasatinib therapy. We report the case of an imatinib intolerant patient who succeeded a complete molecular remission with dasatinib. Dasatinib was stopped bacause of intolerance, but complete molecular remission was sustained for one year and minor molecular remission for 27 months after discontinuation of dasatinib.
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spelling pubmed-35140892012-12-05 Long lasting complete molecular remission after suspending dasatinib treatment in chronic myeloid leukemia Gadó, Klára Matolcsy, András Csomor, Judit Kicsi, Dóra Bödör, Csaba Domján, Gyula Exp Hematol Oncol Letter to the Editor Tyrosine kinase inhibitors specific for BCR-ABL, were a major breakthrough in CML therapy. Second generation tyrosine kinase inhibitors (dasatinib, nilotinib) are indicated for imatinib resistant and intolerant patients. Present guidelines recommend continuous drug dosing for maintaining remission. There is no available data concerning the optimal duration of dasatinib therapy. We report the case of an imatinib intolerant patient who succeeded a complete molecular remission with dasatinib. Dasatinib was stopped bacause of intolerance, but complete molecular remission was sustained for one year and minor molecular remission for 27 months after discontinuation of dasatinib. BioMed Central 2012-07-11 /pmc/articles/PMC3514089/ /pubmed/23210842 http://dx.doi.org/10.1186/2162-3619-1-17 Text en Copyright ©2012 Gado 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 Letter to the Editor
Gadó, Klára
Matolcsy, András
Csomor, Judit
Kicsi, Dóra
Bödör, Csaba
Domján, Gyula
Long lasting complete molecular remission after suspending dasatinib treatment in chronic myeloid leukemia
title Long lasting complete molecular remission after suspending dasatinib treatment in chronic myeloid leukemia
title_full Long lasting complete molecular remission after suspending dasatinib treatment in chronic myeloid leukemia
title_fullStr Long lasting complete molecular remission after suspending dasatinib treatment in chronic myeloid leukemia
title_full_unstemmed Long lasting complete molecular remission after suspending dasatinib treatment in chronic myeloid leukemia
title_short Long lasting complete molecular remission after suspending dasatinib treatment in chronic myeloid leukemia
title_sort long lasting complete molecular remission after suspending dasatinib treatment in chronic myeloid leukemia
topic Letter to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3514089/
https://www.ncbi.nlm.nih.gov/pubmed/23210842
http://dx.doi.org/10.1186/2162-3619-1-17
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