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Therapeutic options for chronic myeloid leukemia: focus on imatinib (Glivec(®), Gleevec™)
Treatment options for chronic myeloid leukemia (CML) have changed dramatically during the last decades. Interferon-α treatment and stem cell transplantation (SCT) clearly improved survival over conventional chemotherapy and offered the possibility of complete and durable responses. With the advent o...
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Formato: | Texto |
Lenguaje: | English |
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Dove Medical Press
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2503652/ https://www.ncbi.nlm.nih.gov/pubmed/18728706 |
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author | Henkes, Martin van der Kuip, Heiko Aulitzky, Walter E |
author_facet | Henkes, Martin van der Kuip, Heiko Aulitzky, Walter E |
author_sort | Henkes, Martin |
collection | PubMed |
description | Treatment options for chronic myeloid leukemia (CML) have changed dramatically during the last decades. Interferon-α treatment and stem cell transplantation (SCT) clearly improved survival over conventional chemotherapy and offered the possibility of complete and durable responses. With the advent of the small molecule inhibitor imatinib mesylate (Glivec(®), Gleevec™) targeting the causative Bcr-Abl oncoprotein, the era of molecular cancer therapy began with remarkable success especially in chronic phase patients. Today, imatinib is the first-line treatment for CML. However, imatinib does not appear to be capable to eliminate all leukemia cells in the patients and pre-existing as well as acquired resistance to the drug has been increasingly recognized. To overcome these problems, several strategies involving dose escalation, combinations with other agents, and novel Bcr-Abl inhibitors have been developed. |
format | Text |
id | pubmed-2503652 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-25036522008-08-26 Therapeutic options for chronic myeloid leukemia: focus on imatinib (Glivec(®), Gleevec™) Henkes, Martin van der Kuip, Heiko Aulitzky, Walter E Ther Clin Risk Manag Review Treatment options for chronic myeloid leukemia (CML) have changed dramatically during the last decades. Interferon-α treatment and stem cell transplantation (SCT) clearly improved survival over conventional chemotherapy and offered the possibility of complete and durable responses. With the advent of the small molecule inhibitor imatinib mesylate (Glivec(®), Gleevec™) targeting the causative Bcr-Abl oncoprotein, the era of molecular cancer therapy began with remarkable success especially in chronic phase patients. Today, imatinib is the first-line treatment for CML. However, imatinib does not appear to be capable to eliminate all leukemia cells in the patients and pre-existing as well as acquired resistance to the drug has been increasingly recognized. To overcome these problems, several strategies involving dose escalation, combinations with other agents, and novel Bcr-Abl inhibitors have been developed. Dove Medical Press 2008-02 2008-02 /pmc/articles/PMC2503652/ /pubmed/18728706 Text en © 2008 Dove Medical Press Limited. All rights reserved |
spellingShingle | Review Henkes, Martin van der Kuip, Heiko Aulitzky, Walter E Therapeutic options for chronic myeloid leukemia: focus on imatinib (Glivec(®), Gleevec™) |
title | Therapeutic options for chronic myeloid leukemia: focus on imatinib (Glivec(®), Gleevec™) |
title_full | Therapeutic options for chronic myeloid leukemia: focus on imatinib (Glivec(®), Gleevec™) |
title_fullStr | Therapeutic options for chronic myeloid leukemia: focus on imatinib (Glivec(®), Gleevec™) |
title_full_unstemmed | Therapeutic options for chronic myeloid leukemia: focus on imatinib (Glivec(®), Gleevec™) |
title_short | Therapeutic options for chronic myeloid leukemia: focus on imatinib (Glivec(®), Gleevec™) |
title_sort | therapeutic options for chronic myeloid leukemia: focus on imatinib (glivec(®), gleevec™) |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2503652/ https://www.ncbi.nlm.nih.gov/pubmed/18728706 |
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