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Prolonged intraperitoneal infusion of 5-fluorouracil using a novel carrier solution.
A novel peritoneal carrier solution, Icodextrin 20 (7.5%), has allowed exploration of prolonged, intraperitoneal (i.p.) infusion of the cytotoxic drug 5-fluorouracil (5-FU). A phase I and pharmacokinetic study was performed to determine the toxicities and maximum tolerated dose of prolonged and cont...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1996
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2074829/ https://www.ncbi.nlm.nih.gov/pubmed/8980409 |
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author | Kerr, D. J. Young, A. M. Neoptolemos, J. P. Sherman, M. Van-Geene, P. Stanley, A. Ferry, D. Dobbie, J. W. Vincke, B. Gilbert, J. el Eini, D. Dombros, N. Fountzilas, G. |
author_facet | Kerr, D. J. Young, A. M. Neoptolemos, J. P. Sherman, M. Van-Geene, P. Stanley, A. Ferry, D. Dobbie, J. W. Vincke, B. Gilbert, J. el Eini, D. Dombros, N. Fountzilas, G. |
author_sort | Kerr, D. J. |
collection | PubMed |
description | A novel peritoneal carrier solution, Icodextrin 20 (7.5%), has allowed exploration of prolonged, intraperitoneal (i.p.) infusion of the cytotoxic drug 5-fluorouracil (5-FU). A phase I and pharmacokinetic study was performed to determine the toxicities and maximum tolerated dose of prolonged and continuous intraperitoneal 5-FU in patients with peritoneal carcinomatosis. Seventeen patients were entered into this study. Each patient had a Tenckhoff catheter placed into the peritoneal cavity under general anaesthetic. After initial flushing and gradual increase in exchange volumes with Icodextrin 20, 5-FU was administered daily from Monday to Friday, 50% as a bolus in the exchange bag and 50% in an elastomeric infusor device delivering continuous 5-FU to the peritoneal cavity at 2 ml h-1. Treatment was continued for 12 weeks or until intolerable toxicity developed. Abdominal pain and infective peritonitis proved to be the main dose-limiting toxicities. Initial problems with infective peritonitis were overcome by redesign of the delivery system, and it proved possible to deliver 300 mg m-2 5-FU daily (5 days per week) for 12 weeks. Pharmacokinetic studies showed i.p. steady-state 5-FU concentrations (mean 47 500 ng ml-1) that were > 1000-fold higher than systemic venous levels (mean 30 ng ml-1). |
format | Text |
id | pubmed-2074829 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1996 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20748292009-09-10 Prolonged intraperitoneal infusion of 5-fluorouracil using a novel carrier solution. Kerr, D. J. Young, A. M. Neoptolemos, J. P. Sherman, M. Van-Geene, P. Stanley, A. Ferry, D. Dobbie, J. W. Vincke, B. Gilbert, J. el Eini, D. Dombros, N. Fountzilas, G. Br J Cancer Research Article A novel peritoneal carrier solution, Icodextrin 20 (7.5%), has allowed exploration of prolonged, intraperitoneal (i.p.) infusion of the cytotoxic drug 5-fluorouracil (5-FU). A phase I and pharmacokinetic study was performed to determine the toxicities and maximum tolerated dose of prolonged and continuous intraperitoneal 5-FU in patients with peritoneal carcinomatosis. Seventeen patients were entered into this study. Each patient had a Tenckhoff catheter placed into the peritoneal cavity under general anaesthetic. After initial flushing and gradual increase in exchange volumes with Icodextrin 20, 5-FU was administered daily from Monday to Friday, 50% as a bolus in the exchange bag and 50% in an elastomeric infusor device delivering continuous 5-FU to the peritoneal cavity at 2 ml h-1. Treatment was continued for 12 weeks or until intolerable toxicity developed. Abdominal pain and infective peritonitis proved to be the main dose-limiting toxicities. Initial problems with infective peritonitis were overcome by redesign of the delivery system, and it proved possible to deliver 300 mg m-2 5-FU daily (5 days per week) for 12 weeks. Pharmacokinetic studies showed i.p. steady-state 5-FU concentrations (mean 47 500 ng ml-1) that were > 1000-fold higher than systemic venous levels (mean 30 ng ml-1). Nature Publishing Group 1996-12 /pmc/articles/PMC2074829/ /pubmed/8980409 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 Kerr, D. J. Young, A. M. Neoptolemos, J. P. Sherman, M. Van-Geene, P. Stanley, A. Ferry, D. Dobbie, J. W. Vincke, B. Gilbert, J. el Eini, D. Dombros, N. Fountzilas, G. Prolonged intraperitoneal infusion of 5-fluorouracil using a novel carrier solution. |
title | Prolonged intraperitoneal infusion of 5-fluorouracil using a novel carrier solution. |
title_full | Prolonged intraperitoneal infusion of 5-fluorouracil using a novel carrier solution. |
title_fullStr | Prolonged intraperitoneal infusion of 5-fluorouracil using a novel carrier solution. |
title_full_unstemmed | Prolonged intraperitoneal infusion of 5-fluorouracil using a novel carrier solution. |
title_short | Prolonged intraperitoneal infusion of 5-fluorouracil using a novel carrier solution. |
title_sort | prolonged intraperitoneal infusion of 5-fluorouracil using a novel carrier solution. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2074829/ https://www.ncbi.nlm.nih.gov/pubmed/8980409 |
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