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Microdialysis and response during regional chemotherapy by isolated limb infusion of melphalan for limb malignancies

This study sought to use a microdialysis technique to relate clinical and biochemical responses to the time course of melphalan concentrations in the subcutaneous interstitial space and in tumour tissue (melanoma, malignant fibrous histiocytoma, Merkel cell tumour and osteosarcoma) in patients under...

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Autores principales: Thompson, J F, Siebert, G A, Anissimov, Y G, Smithers, B M, Doubrovsky, A, Anderson, C D, Roberts, M S
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364039/
https://www.ncbi.nlm.nih.gov/pubmed/11461070
http://dx.doi.org/10.1054/bjoc.2001.1902
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author Thompson, J F
Siebert, G A
Anissimov, Y G
Smithers, B M
Doubrovsky, A
Anderson, C D
Roberts, M S
author_facet Thompson, J F
Siebert, G A
Anissimov, Y G
Smithers, B M
Doubrovsky, A
Anderson, C D
Roberts, M S
author_sort Thompson, J F
collection PubMed
description This study sought to use a microdialysis technique to relate clinical and biochemical responses to the time course of melphalan concentrations in the subcutaneous interstitial space and in tumour tissue (melanoma, malignant fibrous histiocytoma, Merkel cell tumour and osteosarcoma) in patients undergoing regional chemotherapy by Isolated Limb Infusion (ILI). 19 patients undergoing ILI for treatment of various limb malignancies were monitored for intra-operative melphalan concentrations in plasma and, using microdialysis, in subcutaneous and tumour tissues. Peak and mean concentrations of melphalan were significantly higher in plasma than in subcutaneous or tumour microdialysate. There was no significant difference between drug peak and mean concentrations in interstitial and tumour tissue, indicating that there was no preferential uptake of melphalan into the tumours. The time course of melphalan in the microdialysate could be described by a pharmacokinetic model which assumed melphalan distributed from the plasma into the interstitial space. The model also accounted for the vascular dispersion of melphalan in the limb. Tumour response in the whole group to treatment was partial response: 53.8% (n= 7); complete response: 33.3% (n= 5); no response: 6.7% (n= 1). There was a significant association between tumour response and melphalan concentrations measured over time in subcutaneous microdialysate (P< 0.01). No significant relationship existed between the severity of toxic reactions in the limb or peak plasma creatine phosphokinase levels and peak melphalan microdialysate or plasma concentrations. It is concluded that microdialysis is a technique well suited for measuring concentrations of cytotoxic drug during ILI. The possibility of predicting actual concentrations of cytotoxic drug in the limb during ILI using our model opens an opportunity for improved drug dose calculation. The combination of predicting tissue concentrations and monitoring in microdialysate of subcutaneous tissue could help optimise ILI with regard to post-operative limb morbidity and tumour response. © 2001 Cancer Research Campaign http://www.bjcancer.com
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spelling pubmed-23640392009-09-10 Microdialysis and response during regional chemotherapy by isolated limb infusion of melphalan for limb malignancies Thompson, J F Siebert, G A Anissimov, Y G Smithers, B M Doubrovsky, A Anderson, C D Roberts, M S Br J Cancer Regular Article This study sought to use a microdialysis technique to relate clinical and biochemical responses to the time course of melphalan concentrations in the subcutaneous interstitial space and in tumour tissue (melanoma, malignant fibrous histiocytoma, Merkel cell tumour and osteosarcoma) in patients undergoing regional chemotherapy by Isolated Limb Infusion (ILI). 19 patients undergoing ILI for treatment of various limb malignancies were monitored for intra-operative melphalan concentrations in plasma and, using microdialysis, in subcutaneous and tumour tissues. Peak and mean concentrations of melphalan were significantly higher in plasma than in subcutaneous or tumour microdialysate. There was no significant difference between drug peak and mean concentrations in interstitial and tumour tissue, indicating that there was no preferential uptake of melphalan into the tumours. The time course of melphalan in the microdialysate could be described by a pharmacokinetic model which assumed melphalan distributed from the plasma into the interstitial space. The model also accounted for the vascular dispersion of melphalan in the limb. Tumour response in the whole group to treatment was partial response: 53.8% (n= 7); complete response: 33.3% (n= 5); no response: 6.7% (n= 1). There was a significant association between tumour response and melphalan concentrations measured over time in subcutaneous microdialysate (P< 0.01). No significant relationship existed between the severity of toxic reactions in the limb or peak plasma creatine phosphokinase levels and peak melphalan microdialysate or plasma concentrations. It is concluded that microdialysis is a technique well suited for measuring concentrations of cytotoxic drug during ILI. The possibility of predicting actual concentrations of cytotoxic drug in the limb during ILI using our model opens an opportunity for improved drug dose calculation. The combination of predicting tissue concentrations and monitoring in microdialysate of subcutaneous tissue could help optimise ILI with regard to post-operative limb morbidity and tumour response. © 2001 Cancer Research Campaign http://www.bjcancer.com Nature Publishing Group 2001-07 /pmc/articles/PMC2364039/ /pubmed/11461070 http://dx.doi.org/10.1054/bjoc.2001.1902 Text en Copyright © 2001 Cancer Research Campaign 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 Regular Article
Thompson, J F
Siebert, G A
Anissimov, Y G
Smithers, B M
Doubrovsky, A
Anderson, C D
Roberts, M S
Microdialysis and response during regional chemotherapy by isolated limb infusion of melphalan for limb malignancies
title Microdialysis and response during regional chemotherapy by isolated limb infusion of melphalan for limb malignancies
title_full Microdialysis and response during regional chemotherapy by isolated limb infusion of melphalan for limb malignancies
title_fullStr Microdialysis and response during regional chemotherapy by isolated limb infusion of melphalan for limb malignancies
title_full_unstemmed Microdialysis and response during regional chemotherapy by isolated limb infusion of melphalan for limb malignancies
title_short Microdialysis and response during regional chemotherapy by isolated limb infusion of melphalan for limb malignancies
title_sort microdialysis and response during regional chemotherapy by isolated limb infusion of melphalan for limb malignancies
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2364039/
https://www.ncbi.nlm.nih.gov/pubmed/11461070
http://dx.doi.org/10.1054/bjoc.2001.1902
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