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Angiogenesis is an independent prognostic factor in malignant mesothelioma

Angiogenesis is essential for tumour growth beyond 1 to 2 mm in diameter. The clinical relevance of angiogenesis, as assessed by microvessel density (MVD), is unclear in malignant mesothelioma (MM). Immunohistochemistry was performed on 104 archival, paraffin-embedded, surgically resected MM samples...

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Autores principales: Edwards, J G, Cox, G, Andi, A, Jones, J L, Walker, R A, Waller, D A, O'Byrne, K J
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375086/
https://www.ncbi.nlm.nih.gov/pubmed/11556838
http://dx.doi.org/10.1054/bjoc.2001.1997
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author Edwards, J G
Cox, G
Andi, A
Jones, J L
Walker, R A
Waller, D A
O'Byrne, K J
author_facet Edwards, J G
Cox, G
Andi, A
Jones, J L
Walker, R A
Waller, D A
O'Byrne, K J
author_sort Edwards, J G
collection PubMed
description Angiogenesis is essential for tumour growth beyond 1 to 2 mm in diameter. The clinical relevance of angiogenesis, as assessed by microvessel density (MVD), is unclear in malignant mesothelioma (MM). Immunohistochemistry was performed on 104 archival, paraffin-embedded, surgically resected MM samples with an anti-CD34 monoclonal antibody, using the Streptavidin–biotin complex immunoperoxidase technique. 93 cases were suitable for microvessel quantification. MVD was obtained from 3 intratumoural hotspots, using a Chalkley eyepiece graticule at × 250 power. MVD was correlated with survival by Kaplan–Meier and log-rank analysis. A stepwise, multivariate Cox model was used to compare MVD with known prognostic factors and the EORTC and CALGB prognostic scoring systems. Overall median survival from the date of diagnosis was 5.0 months. Increasing MVD was a poor prognostic factor in univariate analysis (P = 0.02). Independent indicators of poor prognosis in multivariate analysis were non-epithelial cell type (P = 0.002), performance status > 0 (P = 0.003) and increasing MVD (P = 0.01). In multivariate Cox analysis, MVD contributed independently to the EORTC (P = 0.006), but not to the CALGB (P = 0.1), prognostic groups. Angiogenesis, as assessed by MVD, is a poor prognostic factor in MM, independent of other clinicopathological variables and the EORTC prognostic scoring system. Further work is required to assess the prognostic importance of angiogenic regulatory factors in this disease. http://www.bjcancer.com © 2001 Cancer Research Campaign  http://www.bjcancer.com
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spelling pubmed-23750862009-09-10 Angiogenesis is an independent prognostic factor in malignant mesothelioma Edwards, J G Cox, G Andi, A Jones, J L Walker, R A Waller, D A O'Byrne, K J Br J Cancer Regular Article Angiogenesis is essential for tumour growth beyond 1 to 2 mm in diameter. The clinical relevance of angiogenesis, as assessed by microvessel density (MVD), is unclear in malignant mesothelioma (MM). Immunohistochemistry was performed on 104 archival, paraffin-embedded, surgically resected MM samples with an anti-CD34 monoclonal antibody, using the Streptavidin–biotin complex immunoperoxidase technique. 93 cases were suitable for microvessel quantification. MVD was obtained from 3 intratumoural hotspots, using a Chalkley eyepiece graticule at × 250 power. MVD was correlated with survival by Kaplan–Meier and log-rank analysis. A stepwise, multivariate Cox model was used to compare MVD with known prognostic factors and the EORTC and CALGB prognostic scoring systems. Overall median survival from the date of diagnosis was 5.0 months. Increasing MVD was a poor prognostic factor in univariate analysis (P = 0.02). Independent indicators of poor prognosis in multivariate analysis were non-epithelial cell type (P = 0.002), performance status > 0 (P = 0.003) and increasing MVD (P = 0.01). In multivariate Cox analysis, MVD contributed independently to the EORTC (P = 0.006), but not to the CALGB (P = 0.1), prognostic groups. Angiogenesis, as assessed by MVD, is a poor prognostic factor in MM, independent of other clinicopathological variables and the EORTC prognostic scoring system. Further work is required to assess the prognostic importance of angiogenic regulatory factors in this disease. http://www.bjcancer.com © 2001 Cancer Research Campaign  http://www.bjcancer.com Nature Publishing Group 2001-09 /pmc/articles/PMC2375086/ /pubmed/11556838 http://dx.doi.org/10.1054/bjoc.2001.1997 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
Edwards, J G
Cox, G
Andi, A
Jones, J L
Walker, R A
Waller, D A
O'Byrne, K J
Angiogenesis is an independent prognostic factor in malignant mesothelioma
title Angiogenesis is an independent prognostic factor in malignant mesothelioma
title_full Angiogenesis is an independent prognostic factor in malignant mesothelioma
title_fullStr Angiogenesis is an independent prognostic factor in malignant mesothelioma
title_full_unstemmed Angiogenesis is an independent prognostic factor in malignant mesothelioma
title_short Angiogenesis is an independent prognostic factor in malignant mesothelioma
title_sort angiogenesis is an independent prognostic factor in malignant mesothelioma
topic Regular Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2375086/
https://www.ncbi.nlm.nih.gov/pubmed/11556838
http://dx.doi.org/10.1054/bjoc.2001.1997
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