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Postchemoembolisation syndrome – tumour necrosis or hepatocyte injury?

Transarterial chemoembolisation of liver tumours is typically followed by elevated body temperature and liver transaminase enzymes. This has often been considered to indicate successful embolisation. The present study questions whether this syndrome reflects damage to tumour cells or to the normal h...

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Autores principales: Wigmore, S J, Redhead, D N, Thomson, B N J, Currie, E J, Parks, R W, Madhavan, K K, Garden, O J
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2394347/
https://www.ncbi.nlm.nih.gov/pubmed/14562011
http://dx.doi.org/10.1038/sj.bjc.6601329
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author Wigmore, S J
Redhead, D N
Thomson, B N J
Currie, E J
Parks, R W
Madhavan, K K
Garden, O J
author_facet Wigmore, S J
Redhead, D N
Thomson, B N J
Currie, E J
Parks, R W
Madhavan, K K
Garden, O J
author_sort Wigmore, S J
collection PubMed
description Transarterial chemoembolisation of liver tumours is typically followed by elevated body temperature and liver transaminase enzymes. This has often been considered to indicate successful embolisation. The present study questions whether this syndrome reflects damage to tumour cells or to the normal hepatic tissue. The responses to 256 embolisations undertaken in 145 patients subdivided into those with hepatocyte-derived (primary hepatocellular carcinoma) and nonhepatocyte-derived tumours (secondary metastases) were analysed to assess the relative effects of tumour necrosis and damage to normal hepatocytes in each group. Cytolysis, measured by elevated alanine aminotransferase, was detected in 85% of patients, and there was no difference in the abnormalities in liver function tests measured between the two groups. Furthermore, cytolysis was associated with a higher rate of postprocedure symptoms and side effects, and elevated temperature was associated with a worse survival on univariate analysis. Multivariate analysis demonstrated that there was no benefit in terms of survival from having elevated temperature or cytolysis following embolisation. Cytolysis after chemoembolisation is probably due to damage to normal hepatocytes. Temperature changes may reflect tumour necrosis or necrosis of the healthy tissue. There is no evidence that either a postchemoembolisation fever or cytolysis is associated with an enhanced tumour response or improved long-term survival in patients with primary or secondary liver cancer.
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spelling pubmed-23943472009-09-10 Postchemoembolisation syndrome – tumour necrosis or hepatocyte injury? Wigmore, S J Redhead, D N Thomson, B N J Currie, E J Parks, R W Madhavan, K K Garden, O J Br J Cancer Clinical Transarterial chemoembolisation of liver tumours is typically followed by elevated body temperature and liver transaminase enzymes. This has often been considered to indicate successful embolisation. The present study questions whether this syndrome reflects damage to tumour cells or to the normal hepatic tissue. The responses to 256 embolisations undertaken in 145 patients subdivided into those with hepatocyte-derived (primary hepatocellular carcinoma) and nonhepatocyte-derived tumours (secondary metastases) were analysed to assess the relative effects of tumour necrosis and damage to normal hepatocytes in each group. Cytolysis, measured by elevated alanine aminotransferase, was detected in 85% of patients, and there was no difference in the abnormalities in liver function tests measured between the two groups. Furthermore, cytolysis was associated with a higher rate of postprocedure symptoms and side effects, and elevated temperature was associated with a worse survival on univariate analysis. Multivariate analysis demonstrated that there was no benefit in terms of survival from having elevated temperature or cytolysis following embolisation. Cytolysis after chemoembolisation is probably due to damage to normal hepatocytes. Temperature changes may reflect tumour necrosis or necrosis of the healthy tissue. There is no evidence that either a postchemoembolisation fever or cytolysis is associated with an enhanced tumour response or improved long-term survival in patients with primary or secondary liver cancer. Nature Publishing Group 2003-10-20 2003-10-14 /pmc/articles/PMC2394347/ /pubmed/14562011 http://dx.doi.org/10.1038/sj.bjc.6601329 Text en Copyright © 2003 Cancer Research UK 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 Clinical
Wigmore, S J
Redhead, D N
Thomson, B N J
Currie, E J
Parks, R W
Madhavan, K K
Garden, O J
Postchemoembolisation syndrome – tumour necrosis or hepatocyte injury?
title Postchemoembolisation syndrome – tumour necrosis or hepatocyte injury?
title_full Postchemoembolisation syndrome – tumour necrosis or hepatocyte injury?
title_fullStr Postchemoembolisation syndrome – tumour necrosis or hepatocyte injury?
title_full_unstemmed Postchemoembolisation syndrome – tumour necrosis or hepatocyte injury?
title_short Postchemoembolisation syndrome – tumour necrosis or hepatocyte injury?
title_sort postchemoembolisation syndrome – tumour necrosis or hepatocyte injury?
topic Clinical
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2394347/
https://www.ncbi.nlm.nih.gov/pubmed/14562011
http://dx.doi.org/10.1038/sj.bjc.6601329
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