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Tipifarnib in the treatment of acute myeloid leukemia
Farnesyltransferase inhibitors (FTIs) are a new class of biologically active anticancer drugs. The exact anti-tumorigenic mechanism is currently unknown. FTIs inhibit farnesylation of a wide range of target proteins. In preclinical models, tipifarnib (R115777, Zarnestra®), a non-peptidomimetic compe...
Autores principales: | , |
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Formato: | Texto |
Lenguaje: | English |
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Dove Medical Press
2007
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2721284/ https://www.ncbi.nlm.nih.gov/pubmed/19707311 |
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author | Thomas, Xavier Elhamri, Mohamed |
author_facet | Thomas, Xavier Elhamri, Mohamed |
author_sort | Thomas, Xavier |
collection | PubMed |
description | Farnesyltransferase inhibitors (FTIs) are a new class of biologically active anticancer drugs. The exact anti-tumorigenic mechanism is currently unknown. FTIs inhibit farnesylation of a wide range of target proteins. In preclinical models, tipifarnib (R115777, Zarnestra®), a non-peptidomimetic competitive FTI, showed great potency against leukemic cells. Although it has recently demonstrated clinical responses in adults with refractory and relapsed acute myeloid leukemia (AML), and in older adults with newly diagnosed poor-risk AML, its activity was far less than anticipated. However, it appears that tipifarnib as a single agent may be important in selected groups of patients. Much remains to be learned to optimize such therapy in patients with AML. To this end, trials that combine tipifarnib with cytotoxics are ongoing. |
format | Text |
id | pubmed-2721284 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2007 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-27212842009-08-25 Tipifarnib in the treatment of acute myeloid leukemia Thomas, Xavier Elhamri, Mohamed Biologics Review Farnesyltransferase inhibitors (FTIs) are a new class of biologically active anticancer drugs. The exact anti-tumorigenic mechanism is currently unknown. FTIs inhibit farnesylation of a wide range of target proteins. In preclinical models, tipifarnib (R115777, Zarnestra®), a non-peptidomimetic competitive FTI, showed great potency against leukemic cells. Although it has recently demonstrated clinical responses in adults with refractory and relapsed acute myeloid leukemia (AML), and in older adults with newly diagnosed poor-risk AML, its activity was far less than anticipated. However, it appears that tipifarnib as a single agent may be important in selected groups of patients. Much remains to be learned to optimize such therapy in patients with AML. To this end, trials that combine tipifarnib with cytotoxics are ongoing. Dove Medical Press 2007-12 2007-12 /pmc/articles/PMC2721284/ /pubmed/19707311 Text en © 2007 Dove Medical Press Limited. All rights reserved |
spellingShingle | Review Thomas, Xavier Elhamri, Mohamed Tipifarnib in the treatment of acute myeloid leukemia |
title | Tipifarnib in the treatment of acute myeloid leukemia |
title_full | Tipifarnib in the treatment of acute myeloid leukemia |
title_fullStr | Tipifarnib in the treatment of acute myeloid leukemia |
title_full_unstemmed | Tipifarnib in the treatment of acute myeloid leukemia |
title_short | Tipifarnib in the treatment of acute myeloid leukemia |
title_sort | tipifarnib in the treatment of acute myeloid leukemia |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2721284/ https://www.ncbi.nlm.nih.gov/pubmed/19707311 |
work_keys_str_mv | AT thomasxavier tipifarnibinthetreatmentofacutemyeloidleukemia AT elhamrimohamed tipifarnibinthetreatmentofacutemyeloidleukemia |