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Intra-Arterial Delivery of Idarubicin in Two Patients with Glioblastoma
There is no effective treatment for recurrent glioblastoma (GB) when temozolomide-based radiochemotherapy fails. In theory, intra-arterial (IA) delivery of cytotoxic agents could achieve higher drug concentrations in tumors compared to intravenous injection. Moreover, choosing a highly lipid-soluble...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
S. Karger AG
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5043287/ https://www.ncbi.nlm.nih.gov/pubmed/27721775 http://dx.doi.org/10.1159/000448654 |
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author | Chehimi, Mohamad Boone, Mathieu Chivot, Cyril Deramond, Hervé Constans, Jean-Marc Ly, Mony Chenda Chauffert, Bruno |
author_facet | Chehimi, Mohamad Boone, Mathieu Chivot, Cyril Deramond, Hervé Constans, Jean-Marc Ly, Mony Chenda Chauffert, Bruno |
author_sort | Chehimi, Mohamad |
collection | PubMed |
description | There is no effective treatment for recurrent glioblastoma (GB) when temozolomide-based radiochemotherapy fails. In theory, intra-arterial (IA) delivery of cytotoxic agents could achieve higher drug concentrations in tumors compared to intravenous injection. Moreover, choosing a highly lipid-soluble drug could make the most of the first-pass effect. Here, we evaluated idarubicin (IDA), a lipophilic anthracycline, in an in vitro assay using four human GB cell lines and compared it with 11 other drugs previously used for the IA treatment of brain tumors. Despite impressive in vitro cytotoxicity, IA IDA did not produce a beneficial effect in 2 patients with recurrent GB. |
format | Online Article Text |
id | pubmed-5043287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | S. Karger AG |
record_format | MEDLINE/PubMed |
spelling | pubmed-50432872016-10-07 Intra-Arterial Delivery of Idarubicin in Two Patients with Glioblastoma Chehimi, Mohamad Boone, Mathieu Chivot, Cyril Deramond, Hervé Constans, Jean-Marc Ly, Mony Chenda Chauffert, Bruno Case Rep Oncol Case Report There is no effective treatment for recurrent glioblastoma (GB) when temozolomide-based radiochemotherapy fails. In theory, intra-arterial (IA) delivery of cytotoxic agents could achieve higher drug concentrations in tumors compared to intravenous injection. Moreover, choosing a highly lipid-soluble drug could make the most of the first-pass effect. Here, we evaluated idarubicin (IDA), a lipophilic anthracycline, in an in vitro assay using four human GB cell lines and compared it with 11 other drugs previously used for the IA treatment of brain tumors. Despite impressive in vitro cytotoxicity, IA IDA did not produce a beneficial effect in 2 patients with recurrent GB. S. Karger AG 2016-08-30 /pmc/articles/PMC5043287/ /pubmed/27721775 http://dx.doi.org/10.1159/000448654 Text en Copyright © 2016 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission. |
spellingShingle | Case Report Chehimi, Mohamad Boone, Mathieu Chivot, Cyril Deramond, Hervé Constans, Jean-Marc Ly, Mony Chenda Chauffert, Bruno Intra-Arterial Delivery of Idarubicin in Two Patients with Glioblastoma |
title | Intra-Arterial Delivery of Idarubicin in Two Patients with Glioblastoma |
title_full | Intra-Arterial Delivery of Idarubicin in Two Patients with Glioblastoma |
title_fullStr | Intra-Arterial Delivery of Idarubicin in Two Patients with Glioblastoma |
title_full_unstemmed | Intra-Arterial Delivery of Idarubicin in Two Patients with Glioblastoma |
title_short | Intra-Arterial Delivery of Idarubicin in Two Patients with Glioblastoma |
title_sort | intra-arterial delivery of idarubicin in two patients with glioblastoma |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5043287/ https://www.ncbi.nlm.nih.gov/pubmed/27721775 http://dx.doi.org/10.1159/000448654 |
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