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Pharmacokinetic interaction between epirubicin and the multidrug resistance reverting agent D-verapamil.
The potential for a pharmacokinetic interaction between epirubicin and the second-generation multidrug resistance modulating agent D-verapamil (DVPM) has been investigated in six patients with advanced colorectal cancer. Our results indicate that a significant interaction takes place. Enhanced distr...
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
1993
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1968306/ https://www.ncbi.nlm.nih.gov/pubmed/8318424 |
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author | Scheithauer, W. Schenk, T. Czejka, M. |
author_facet | Scheithauer, W. Schenk, T. Czejka, M. |
author_sort | Scheithauer, W. |
collection | PubMed |
description | The potential for a pharmacokinetic interaction between epirubicin and the second-generation multidrug resistance modulating agent D-verapamil (DVPM) has been investigated in six patients with advanced colorectal cancer. Our results indicate that a significant interaction takes place. Enhanced distribution of epirubicin from the serum and altered disposition might, in fact, explain the increased level of myelotoxicity in this pilot as well as in other clinical phase II studies involving DVPM. |
format | Text |
id | pubmed-1968306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1993 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-19683062009-09-10 Pharmacokinetic interaction between epirubicin and the multidrug resistance reverting agent D-verapamil. Scheithauer, W. Schenk, T. Czejka, M. Br J Cancer Research Article The potential for a pharmacokinetic interaction between epirubicin and the second-generation multidrug resistance modulating agent D-verapamil (DVPM) has been investigated in six patients with advanced colorectal cancer. Our results indicate that a significant interaction takes place. Enhanced distribution of epirubicin from the serum and altered disposition might, in fact, explain the increased level of myelotoxicity in this pilot as well as in other clinical phase II studies involving DVPM. Nature Publishing Group 1993-07 /pmc/articles/PMC1968306/ /pubmed/8318424 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Scheithauer, W. Schenk, T. Czejka, M. Pharmacokinetic interaction between epirubicin and the multidrug resistance reverting agent D-verapamil. |
title | Pharmacokinetic interaction between epirubicin and the multidrug resistance reverting agent D-verapamil. |
title_full | Pharmacokinetic interaction between epirubicin and the multidrug resistance reverting agent D-verapamil. |
title_fullStr | Pharmacokinetic interaction between epirubicin and the multidrug resistance reverting agent D-verapamil. |
title_full_unstemmed | Pharmacokinetic interaction between epirubicin and the multidrug resistance reverting agent D-verapamil. |
title_short | Pharmacokinetic interaction between epirubicin and the multidrug resistance reverting agent D-verapamil. |
title_sort | pharmacokinetic interaction between epirubicin and the multidrug resistance reverting agent d-verapamil. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1968306/ https://www.ncbi.nlm.nih.gov/pubmed/8318424 |
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