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High survivin expression as a risk factor in patients with anal carcinoma treated with concurrent chemoradiotherapy
PURPOSE: To investigate the prognostic value of survivin expression in pretreatment specimens from patients with anal cancer treated with concurrent 5-FU and mitomycin C-based chemoradiation (CRT). MATERIAL AND METHODS: Immunohistochemical staining for survivin was performed in pretreatment biopsies...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3430559/ https://www.ncbi.nlm.nih.gov/pubmed/22697293 http://dx.doi.org/10.1186/1748-717X-7-88 |
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author | Fraunholz, Ingeborg Rödel, Claus Distel, Luitpold Rave-Fränk, Marget Kohler, Daniela Falk, Stefan Rödel, Franz |
author_facet | Fraunholz, Ingeborg Rödel, Claus Distel, Luitpold Rave-Fränk, Marget Kohler, Daniela Falk, Stefan Rödel, Franz |
author_sort | Fraunholz, Ingeborg |
collection | PubMed |
description | PURPOSE: To investigate the prognostic value of survivin expression in pretreatment specimens from patients with anal cancer treated with concurrent 5-FU and mitomycin C-based chemoradiation (CRT). MATERIAL AND METHODS: Immunohistochemical staining for survivin was performed in pretreatment biopsies of 62 patients with anal carcinoma. Survivin expression was correlated with clinical and histopathological characteristics as well as local failure free- (LFFS), distant metastases free- (DMFS), cancer specific- (CSS), and overall survival (OS). RESULTS: Survivin staining intensity was weak in 10%, intermediate in 48% and intense in 42% of the patients. No association between survivin expression and clinicopathologic factors (tumor stage, age and HIV status) could be shown. In univariate analysis, the level of survivin staining was significantly correlated with DMFS (low survivin vs. high survivin: 94% vs. 74%, p = 0.04). T-stage, N-stage and the tumor grading were significantly associated with OS and CSS and with DMFS and LFFS, respectively. In multivariate analysis, survivin was confirmed as independent prognostic parameter for DMFS (RR, 0.04; p = 0.02) and for OS (RR, 0.27; p = 0.04). CONCLUSION: Our results demonstrated that the level of pretreatment survivin is correlated with the clinical outcome in patients with anal carcinoma treated with concurrent CRT. Further studies are warranted to elucidate the complex role of survivin for the oncologic treatment and to exploit the protein as a therapeutic target in combined modality treatment of anal cancer. |
format | Online Article Text |
id | pubmed-3430559 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-34305592012-08-30 High survivin expression as a risk factor in patients with anal carcinoma treated with concurrent chemoradiotherapy Fraunholz, Ingeborg Rödel, Claus Distel, Luitpold Rave-Fränk, Marget Kohler, Daniela Falk, Stefan Rödel, Franz Radiat Oncol Research PURPOSE: To investigate the prognostic value of survivin expression in pretreatment specimens from patients with anal cancer treated with concurrent 5-FU and mitomycin C-based chemoradiation (CRT). MATERIAL AND METHODS: Immunohistochemical staining for survivin was performed in pretreatment biopsies of 62 patients with anal carcinoma. Survivin expression was correlated with clinical and histopathological characteristics as well as local failure free- (LFFS), distant metastases free- (DMFS), cancer specific- (CSS), and overall survival (OS). RESULTS: Survivin staining intensity was weak in 10%, intermediate in 48% and intense in 42% of the patients. No association between survivin expression and clinicopathologic factors (tumor stage, age and HIV status) could be shown. In univariate analysis, the level of survivin staining was significantly correlated with DMFS (low survivin vs. high survivin: 94% vs. 74%, p = 0.04). T-stage, N-stage and the tumor grading were significantly associated with OS and CSS and with DMFS and LFFS, respectively. In multivariate analysis, survivin was confirmed as independent prognostic parameter for DMFS (RR, 0.04; p = 0.02) and for OS (RR, 0.27; p = 0.04). CONCLUSION: Our results demonstrated that the level of pretreatment survivin is correlated with the clinical outcome in patients with anal carcinoma treated with concurrent CRT. Further studies are warranted to elucidate the complex role of survivin for the oncologic treatment and to exploit the protein as a therapeutic target in combined modality treatment of anal cancer. BioMed Central 2012-06-14 /pmc/articles/PMC3430559/ /pubmed/22697293 http://dx.doi.org/10.1186/1748-717X-7-88 Text en Copyright ©2012 Fraunholz et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Fraunholz, Ingeborg Rödel, Claus Distel, Luitpold Rave-Fränk, Marget Kohler, Daniela Falk, Stefan Rödel, Franz High survivin expression as a risk factor in patients with anal carcinoma treated with concurrent chemoradiotherapy |
title | High survivin expression as a risk factor in patients with anal carcinoma treated with concurrent chemoradiotherapy |
title_full | High survivin expression as a risk factor in patients with anal carcinoma treated with concurrent chemoradiotherapy |
title_fullStr | High survivin expression as a risk factor in patients with anal carcinoma treated with concurrent chemoradiotherapy |
title_full_unstemmed | High survivin expression as a risk factor in patients with anal carcinoma treated with concurrent chemoradiotherapy |
title_short | High survivin expression as a risk factor in patients with anal carcinoma treated with concurrent chemoradiotherapy |
title_sort | high survivin expression as a risk factor in patients with anal carcinoma treated with concurrent chemoradiotherapy |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3430559/ https://www.ncbi.nlm.nih.gov/pubmed/22697293 http://dx.doi.org/10.1186/1748-717X-7-88 |
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