Chronic myelogenous leukemia: the present and the future of the TKI therapy

Impressive response rates and the good tolerability have allowed imatinib to become the gold standard frontline therapy for all CML patients in the early chronic phase. Optimal outcomes are attained with more than two thirds of the CML cases treated with standard dose imatinib (400 mg daily). Criteria to establish failure and suboptimal responses to imatinib have been defined. Treatment guidelines have also suggested imatinib dose escalation based on clinical assessments of disease response. However, despite all the effort to optimize therapy with imatinib, cases of real resistance exist. For imatinib resistant and intolerant cases, second generation powerful tyrosine kinase inhibitors (TKIs) have been developed and registered. Sequential kinase inhibitor therapy is used to overcome resistance however, a future strategy might be a combination therapy with different ABL kinase inhibitors in the same therapeutic scheme, used sequentially or simultaneousl.

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Main Authors: Saglio,Giuseppe, Fava,Carmen
Format: Digital revista
Language:English
Published: Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular 2009
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842009000800015
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spelling oai:scielo:S1516-848420090008000152009-09-29Chronic myelogenous leukemia: the present and the future of the TKI therapySaglio,GiuseppeFava,Carmen Chronic myeloid leukemia TKi inhibitor resistence and intolerance Impressive response rates and the good tolerability have allowed imatinib to become the gold standard frontline therapy for all CML patients in the early chronic phase. Optimal outcomes are attained with more than two thirds of the CML cases treated with standard dose imatinib (400 mg daily). Criteria to establish failure and suboptimal responses to imatinib have been defined. Treatment guidelines have also suggested imatinib dose escalation based on clinical assessments of disease response. However, despite all the effort to optimize therapy with imatinib, cases of real resistance exist. For imatinib resistant and intolerant cases, second generation powerful tyrosine kinase inhibitors (TKIs) have been developed and registered. Sequential kinase inhibitor therapy is used to overcome resistance however, a future strategy might be a combination therapy with different ABL kinase inhibitors in the same therapeutic scheme, used sequentially or simultaneousl.info:eu-repo/semantics/openAccessAssociação Brasileira de Hematologia e Hemoterapia e Terapia CelularRevista Brasileira de Hematologia e Hemoterapia v.31 suppl.2 20092009-08-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842009000800015en10.1590/S1516-84842009000800015
institution SCIELO
collection OJS
country Brasil
countrycode BR
component Revista
access En linea
databasecode rev-scielo-br
tag revista
region America del Sur
libraryname SciELO
language English
format Digital
author Saglio,Giuseppe
Fava,Carmen
spellingShingle Saglio,Giuseppe
Fava,Carmen
Chronic myelogenous leukemia: the present and the future of the TKI therapy
author_facet Saglio,Giuseppe
Fava,Carmen
author_sort Saglio,Giuseppe
title Chronic myelogenous leukemia: the present and the future of the TKI therapy
title_short Chronic myelogenous leukemia: the present and the future of the TKI therapy
title_full Chronic myelogenous leukemia: the present and the future of the TKI therapy
title_fullStr Chronic myelogenous leukemia: the present and the future of the TKI therapy
title_full_unstemmed Chronic myelogenous leukemia: the present and the future of the TKI therapy
title_sort chronic myelogenous leukemia: the present and the future of the tki therapy
description Impressive response rates and the good tolerability have allowed imatinib to become the gold standard frontline therapy for all CML patients in the early chronic phase. Optimal outcomes are attained with more than two thirds of the CML cases treated with standard dose imatinib (400 mg daily). Criteria to establish failure and suboptimal responses to imatinib have been defined. Treatment guidelines have also suggested imatinib dose escalation based on clinical assessments of disease response. However, despite all the effort to optimize therapy with imatinib, cases of real resistance exist. For imatinib resistant and intolerant cases, second generation powerful tyrosine kinase inhibitors (TKIs) have been developed and registered. Sequential kinase inhibitor therapy is used to overcome resistance however, a future strategy might be a combination therapy with different ABL kinase inhibitors in the same therapeutic scheme, used sequentially or simultaneousl.
publisher Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular
publishDate 2009
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842009000800015
work_keys_str_mv AT sagliogiuseppe chronicmyelogenousleukemiathepresentandthefutureofthetkitherapy
AT favacarmen chronicmyelogenousleukemiathepresentandthefutureofthetkitherapy
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